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Genetic Aberrations of DNA Repair Pathways in Prostate Cancer: Translation to the Clinic
Prostate most cancers (PC) is the second most typical most cancers in males worldwide. Because of the large-scale sequencing efforts, there may be presently a greater understanding of the genomic panorama of PC. The identification of defects in DNA restore genes has led to medical research that present a powerful rationale for growing poly (ADP-ribose) polymerase (PARP) inhibitors and DNA-damaging brokers on this molecularly outlined subset of sufferers.
The identification of molecularly outlined subgroups of sufferers has additionally different medical implications; for instance, we now know that carriers of breast most cancers 2 (BRCA2) pathogenic sequence variants (PSVs) have elevated ranges of serum prostate particular antigen (PSA) at analysis, elevated proportion of excessive Gleason tumors, elevated charges of nodal and distant metastases, and excessive recurrence fee; BRCA2 PSVs confer decrease general survival (OS). Distinct tumor PSV, methylation, and expression patterns have been recognized in BRCA2 in contrast with non-BRCA2 mutant prostate tumors.
A number of DNA injury response and restore (DDR)-targeting brokers are presently being evaluated both as single brokers or together in sufferers with PC. On this overview article, we spotlight the biology and medical implications of deleterious inherited or acquired DNA restore pathway aberrations in PC and provide an outline of recent brokers being developed for the remedy of PC.

Analyzing Plant Gene Focusing on Outcomes and Conversion Tracts with Nanopore Sequencing

The high-throughput molecular evaluation of gene concentrating on (GT) occasions is made technically difficult by the residual presetabce of donor molecules. Giant donor molecules prohibit primer placement, leading to lengthy amplicons that can’t be readily analyzed utilizing customary NGS pipelines or qPCR-based approaches resembling ddPCR. In crops, removing of extra donor is time and useful resource intensive, typically requiring plant regeneration and weeks to months of effort.
Right here, we utilized Oxford Nanopore Amplicon Sequencing (ONAS) to bypass the constraints imposed by donor molecules with 1 kb of homology to the goal and dissected GT outcomes at three loci in Nicotiana benthamia leaves. We developed a novel bioinformatic pipeline, Phased ANalysis of Genome Modifying Amplicons (PANGEA), to cut back the impact of ONAS error on amplicon evaluation and captured tens of 1000’s of somatic plant GT occasions.
Moreover, PANGEA allowed us to gather 1000’s of GT conversion tracts 5 days after reagent supply with no choice, revealing that almost all occasions utilized tracts lower than 100 bp in size when incorporating an 18 bp or three bp insertion. These knowledge reveal the usefulness of ONAS and PANGEA for plant GT evaluation and supply a mechanistic foundation for future plant GT optimization.

Genome Sequence Evaluation of the Fungal Pathogen Fusarium graminearum Utilizing Oxford Nanopore Know-how

Fusarium graminearum is a plant pathogen of world significance which causes not solely important yield loss but additionally crop spoilage as a consequence of mycotoxins that render grain unsafe for human or livestock consumption. Though the complete genome of a number of F. graminearum isolates from completely different elements of the world have been sequenced, there aren’t any comparable research of isolates originating from China.
The present research sought to deal with this by sequencing the F. graminearum isolate FG-12, which was remoted from the roots of maize seedlings exhibiting typical signs of blight rising within the Gansu province, China, utilizing Oxford Nanopore Know-how (ONT). The FG-12 isolate was discovered to have a 35.9 Mb genome comprised of 5 scaffolds comparable to the 4 chromosomes and mitochondrial DNA of the F. graminearum sort pressure, PH-1.
The genome was discovered to comprise an roughly 2.23% repetitive sequence and encode 12,470 predicted genes. Extra bioinformatic evaluation recognized 437 genes that had been predicted to be secreted effectors, certainly one of which was confirmed to set off a hypersensitive responses (HR) within the leaves of Nicotiana benthamiana throughout transient expression experiments using agro-infiltration. The F. graminearum FG-12 genome sequence and annotation knowledge produced within the present research present a particularly helpful useful resource for each intra- and inter-species comparative analyses in addition to for gene purposeful research, and will enormously advance our understanding of this essential plant pathogen.
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Prevalence of Virulence Genes and Antimicrobial Resistance of E. coli O157:H7 Remoted from the Beef Carcass of Bahir Dar Metropolis, Ethiopia

Ecoli O157:H7 is among the most virulent foodborne pathogens. The purpose of this research was to isolate E. coli O157:H7, decide virulence genes carried by the organism, and assess the antimicrobial susceptibility sample of the isolates from beef carcass samples at Bahir Dar metropolis. Swab samples (n = 280) had been collected from the carcass of cattle slaughtered on the abattoir and processed utilizing sorbitol MacConkey agar supplemented with cefixime telluride and confirmed with latex agglutination take a look at.
A polymerase chain response was carried out on isolates for the detection of virulence genes stx1stx2hlyA, and eae. Antimicrobial susceptibility testing was carried out utilizing the disk diffusion technique. Of 280 samples processed, 25 (8.9%) isolates had been optimistic. Out of 25 isolates subjected for molecular detection, 8 (32%) and 14 (56%) isolates possessed stx1 and stx2 genes, respectively; from these, 5 (20%) isolates had each genes for the manufacturing of Shiga toxins.
In contrast from different virulent genes comparatively increased proportion of 18 (72%) isolates carried the hlyA gene. Solely 5 (2%) isolates had been optimistic for eae. Resistance was detected in all 25 (100%) isolates and three (12%) towards clindamycin and trimethoprim, respectively. This research end result highlights the potential risk to public well being. The abattoir staff should be conscious concerning the pathogen and may comply with applicable practices to stop contamination of meat supposed for human consumption.

Genome-scale RNAi screens in African trypanosomes

Genome-scale genetic screens enable researchers to quickly establish the genes and proteins that influence a specific phenotype of curiosity. In African trypanosomes, RNA interference (RNAi) knockdown screens have revealed mechanisms underpinning drug resistance, drug transport, prodrug metabolism, quorum sensing, genome replication, and gene expression management.
RNAi screening has additionally been remarkably efficient at highlighting promising potential antitrypanosomal drug targets. The primary ever RNAi library display was applied in African trypanosomes, and genome-scale RNAi screens and different associated approaches proceed to have a serious influence on trypanosomatid analysis. Right here, I overview these impacts when it comes to each discovery and translation.
The latest software of macroecological instruments and ideas has made it potential to establish constant patterns within the distribution of microbial biodiversity, which enormously improved our understanding of the microbial world at massive scales. Nevertheless, the distribution of microbial capabilities stays largely uncharted from the macroecological perspective. Right here, we used macroecological fashions to look at how the genes encoding the purposeful capabilities of microorganisms are distributed inside and throughout soil methods.
Fashions constructed utilizing purposeful gene array knowledge from 818 soil microbial communities confirmed that the occupancy-frequency distributions of genes had been bimodal in each studied website, and that their rank-abundance distributions had been finest described by a lognormal mannequin. As well as, the relationships between gene occupancy and abundance had been optimistic in all websites.
This allowed us to establish genes with excessive abundance and ubiquitous distribution (core) and genes with low abundance and restricted spatial distribution (satellites), and to indicate that they encode completely different units of microbial traits. Widespread genes encode microbial traits associated to the primary biogeochemical cycles (C, N, P and S) whereas uncommon genes encode traits associated to adaptation to environmental stresses, resembling nutrient limitation, resistance to heavy metals and degradation of xenobiotics.
Total, this research characterised for the primary time the distribution of microbial purposeful genes inside soil methods, and spotlight the curiosity of macroecological fashions for understanding the purposeful group of microbial methods throughout spatial scales.
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Postharvest Treatment of Hydrogen Sulfide Delays the Softening of Chilean Strawberry Fruit by Downregulating the Expression of Key Genes Involved in Pectin Catabolism
Hydrogen sulfide (H2S) performs a number of physiological roles in crops. Regardless of the proof, the position of H2S on cell wall disassembly and its implications on fleshy fruit firmness stays unknown. On this work, the impact of H2S therapy on the shelf-life, cell wall polymers and cell wall modifying-related gene expression of Chilean strawberry (Fragaria chiloensis) fruit was examined throughout postharvest storage.
The therapy with H2S extended the shelf-life of fruit by an impact of optimum dose. Fruit handled with 0.2 mM H2S maintained considerably increased fruit firmness than non-treated fruit, lowering its decay and tripling its shelf-life. Moreover, H2S therapy delays pectin degradation all through the storage interval and considerably downregulated the expression of genes encoding for pectinases, corresponding to polygalacturonase, pectate lyase, and expansin.
This proof means that H2S as a gasotransmitter prolongs the post-harvest shelf-life of the fruit and prevents its quick softening fee by a downregulation of the expression of key pectinase genes, which results in a decreased pectin degradation.

The Lipid-Modulating Impact of Tangeretin on the Inhibition of Angiopoietin-like 3 (ANGPTL3) Gene Expression via Regulation of LXRα Activation in Hepatic Cells

The extreme accumulation of TG-rich lipoproteins (TGRLs) in plasma is related to dyslipidemia and atherosclerotic cardiovascular illnesses (ASCVDs). Tangeretin is a bioactive pentamethoxyflavone primarily present in citrus peels, and it has been reported to guard towards hyperlipidemia, diabetes, and weight problems. The intention of this examine was to research the lipid-modulating results and the underlying mechanisms of tangeretin motion in hepatic cells.
Transcriptome and bioinformatics analyses with the Gene Ontology (GO) database confirmed that tangeretin considerably regulated a set of 13 differentially expressed genes (DEGs) related to the regulation of lipoprotein lipase (LPL) exercise. Amongst these DEGs, angiopoietin-like 3 (ANGPTL3), an important inhibitor of LPL catalytic exercise that regulates TGRL metabolism in plasma, was markedly downregulated by tangeretin. We demonstrated that tangeretin considerably inhibited the mRNA expression of ANGPTL3 in HepG2 and Huh-7 cells. Tangeretin therapy of hepatic cells additionally lowered the degrees of each intracellular and secreted ANGPTL3 proteins. Furthermore, we discovered that inhibition of ANGPTL3 manufacturing by tangeretin augmented LPL exercise.
We additional demonstrated that the transcriptional exercise of the ANGPTL3 promoter was considerably attenuated by tangeretin, and we recognized a DNA aspect positioned between the -250 and -121 positions that responded to tangeretin. Moreover, we discovered that tangeretin didn’t alter the degrees of the nuclear liver X receptor α (LXRα) protein, an important transcription issue that binds to the tangeretin-responsive aspect, however it could actually counteract LXRα-mediated ANGPTL3 transcription.
On the premise of molecular docking evaluation, tangeretin was predicted to bind to the ligand-binding area of LXRα, which might lead to suppression of LXRα activation. Our findings help the speculation that tangeretin exerts a lipid-lowering impact by modulating the LXRα-ANGPTL3-LPL pathway, and thus, it may be used as a possible phytochemical for the prevention or therapy of dyslipidemia.

Factors of View on the Instruments for Genome/Gene Modifying

Theoretically, a DNA sequence-specific recognition protein that may distinguish a DNA sequence equal to or greater than 16 bp might be distinctive to mammalian genomes. Lengthy-sequence-specific nucleases, corresponding to naturally occurring Homing Endonucleases and artificially engineered ZFN, TALEN, and Cas9-sgRNA, have been developed and broadly utilized in genome enhancing. In distinction to different counterparts, which acknowledge DNA goal websites by the protein moieties themselves, Cas9 makes use of a single-guide RNA (sgRNA) as a template for DNA goal recognition.
As a result of simplicity in designing and synthesizing a sgRNA for a goal website, Cas9-sgRNA has turn into essentially the most present software for genome enhancing. Furthermore, the RNA-guided DNA recognition exercise of Cas9-sgRNA is impartial of each of the nuclease actions of it on the complementary strand by the HNH area and the non-complementary strand by the RuvC area, and HNH nuclease exercise null mutant (H840A) and RuvC nuclease exercise null mutant (D10A) had been recognized.
In accompaniment with the sgRNA, Cas9, Cas9(D10A), Cas9(H840A), and Cas9(D10A, H840A) can be utilized to attain double strand breakage, complementary strand breakage, non-complementary strand breakage, and no breakage on-target website, respectively. Based mostly on such distinctive traits, many engineered enzyme actions, corresponding to DNA methylation, histone methylation, histone acetylation, cytidine deamination, adenine deamination, and primer-directed mutation, might be launched inside or across the goal website.
In an effort to stop off-targeting by the lasting expression of Cas9 derivatives, numerous transient expression strategies, together with the direct supply of Cas9-sgRNA riboprotein, had been developed. The difficulty of biosafety is indispensable in in vivo purposes; Cas9-sgRNA packaged into virus-like particles or extracellular vesicles have been designed and a few in vivo therapeutic trials have been reported.
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De Novo Transcriptome Meeting, Practical Annotation, and Transcriptome Dynamics Analyses Reveal Stress Tolerance Genes in Mangrove Tree ( Bruguiera gymnorhiza)

Their excessive adaptability to troublesome coastal circumstances makes mangrove bushes a precious useful resource and an fascinating mannequin system for understanding the molecular mechanisms underlying stress tolerance and adaptation of crops to the annoying environmental circumstances. On this examine, we used RNA sequencing (RNA-Seq) for de novo assembling and characterizing the Bruguiera gymnorhiza (L.) Lamk leaf transcriptome. B. gymnorhiza is likely one of the most generally distributed mangrove species from the largest household of mangroves; Rhizophoraceae. The de novo meeting was adopted by useful annotations and identification of particular person transcripts and gene households which are concerned in abiotic stress response.
We then in contrast the genome-wide expression profiles between two populations of B. gymnorhiza, rising beneath totally different ranges of stress, of their pure habitats. One inhabitants residing in excessive salinity atmosphere, within the shore of the Pacific Ocean- Japan, and the opposite inhabitants residing about one kilometre farther from the ocean, and subsequent to the estuary of a river; in much less saline and extra brackish situation.
Many genes concerned in response to salt and osmotic stress, confirmed elevated expression ranges in bushes rising subsequent to the ocean in excessive salinity situation. Validation of those genes might contribute to future salt-resistance analysis in mangroves and different woody crops. Moreover, the sequences and transcriptome information offered on this examine are precious scientific assets for future comparative transcriptome analysis in crops rising beneath annoying circumstances.

 

 

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The Effect of Water Deficit on Two Greek Vitis vinifera L. Cultivars: Physiology, Grape Composition and Gene Expression during Berry Development
Vegetation are uncovered to quite a few abiotic stresses. Drought might be crucial of them and determines crop distribution world wide. Grapevine is taken into account to be a drought-resilient species, historically overlaying semiarid areas. Furthermore, within the case of grapevine, average water deficit is thought to enhance the standard traits of grape berries and subsequently wine composition.
Nonetheless, in opposition to the backdrop of local weather change, vines are anticipated to expertise sustained water deficits which may very well be detrimental to each grape high quality and yield. The affect of water deficit on two Greek Vitis vinifera L. cultivars, ‘Agiorgitiko’ and ‘Assyrtiko’, was investigated in the course of the 2019 and 2020 vintages. Vine physiology measurements in irrigated and non-irrigated crops have been carried out at three time-points all through berry improvement (inexperienced berry, veraison and harvest).
Berry progress and composition have been examined throughout ripening. In response to the outcomes, water deficit resulted in diminished berry dimension and elevated ranges of soluble sugars, whole phenols and anthocyanins. The expression profile of particular genes, recognized to manage grape coloration, aroma and taste was altered by water availability throughout maturation in a cultivar-specific method.
In settlement with the elevated focus of phenolic compounds attributable to water deficit, genes of the phenylpropanoid pathway within the red-skinned Agiorgitiko exhibited greater expression ranges and earlier up-regulation than within the white Assyrtiko. The expression profile of the opposite genes throughout maturation or in response to water deficit was relied on the classic.

Figuring out Clinicopathological Elements Related to Oncotype DX  21-Gene Recurrence Rating: A Actual-World Retrospective Cohort Examine of Breast Most cancers Sufferers in Quebec Metropolis, Canada

Gene expression profiling assessments such because the Oncotype DX (ODX) 21-gene recurrence rating (RS) assay is more and more utilized in medical follow to foretell the chance of recurrence and assist therapy planning for early-stage breast most cancers (BC). Nonetheless, this check has some disadvantages similar to a excessive value and an extended turnaround time to get outcomes, which can result in disparities in entry. We intention to determine clinicopathological components related to ODX RS in girls with early-stage BC. We performed a retrospective cohort examine of girls recognized within the medical database of the Deschênes-Fabia Breast Illness Middle of Quebec Metropolis College, Canada. Our pattern consists of 425 girls identified with early-stage BC who’ve obtained an ODX RS between January 2011 and April 2015. The ODX RS has been categorized into three ranges as initially outlined: low (0-17), intermediate (18-30), and excessive (>30). The imply RS was 17.8 (SD = 9.2).
Univariate analyses and multinomial logistic regressions have been carried out to determine components related to intermediate and excessive RS in contrast with low RS. A complete of 237 (55.8%) sufferers had low RS, 148 (34.8%) had intermediate RS, and 40 (9.4%) had excessive RS. Girls with progesterone receptor (PR)-negative (ORs starting from 3.51 to 10.34) and histologic grade II (ORs starting from 3.16 to 23.04) tumors have been constantly extra prone to have intermediate or excessive RS than low RS. Comparable patterns of associations have been noticed when the RS was categorised utilizing redefined thresholds from (i.e., from the TAILORx examine or dichotomized).
This examine gives proof suggesting that histologic grade and PR standing are predictive components for intermediate or excessive RS in girls with early-stage BC. If these outcomes are confirmed in future research, contemplating these clinicopathological components may spare girls the necessity to get such a check earlier than the start of a doable adjuvant remedy. This feature may very well be thought of in settings the place the price of testing is a matter.
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Gene Evaluation, Cloning, and Heterologous Expression of Protease from a Micromycete Aspergillus ochraceus Able to Activating Protein C of Blood Plasma

Micromycetes are recognized to secrete quite a few enzymes of biotechnological and medical potential. Fibrinolytic protease-activator of protein C (PAPC) of blood plasma from micromycete Aspergillus ochraceus VKM-F4104D was obtained in recombinant type utilising the bacterial expression system. This enzyme, which belongs to the proteinase-Ok-like proteases, is much like the proteases encoded within the genomes of Aspergillus fumigatus ATCC MYA-4609, A. oryzae ATCC 42149 and A. flavus 28.
Mature PAPC-4104 is 282 amino acids lengthy, preceded by the 101-amino acid propeptide crucial for correct folding and maturation. The recombinant protease was similar to the native enzyme from micromycete by way of its organic properties, together with a capability to hydrolyse substrates of activated protein C (pGlu-Professional-Arg-pNA) and issue Xa (Z-D-Arg-Gly-Arg-pNA) in conjugant reactions with human blood plasma.
Subsequently, recombinant PAPC-4104 can probably be utilized in medication, veterinary science, diagnostics, and different purposes. Useful annotation of unknown operate genes reveals unidentified features that may improve our understanding of advanced genome communications. A typical method for inferring gene operate entails the ortholog-based methodology. Nonetheless, genetic information alone are sometimes not sufficient to offer data for operate annotation.
Thus, integrating different sources of knowledge can probably improve the potential for retrieving annotations. Community-based strategies are environment friendly strategies for exploring interactions amongst genes and can be utilized for practical inference. On this examine, we current an evaluation framework for inferring the features of Plasmodium falciparum genes primarily based on connection profiles in a heterogeneous community between human and Plasmodium falciparum proteins. These profiles have been fed right into a hybrid deep studying algorithm to foretell the orthologs of unknown operate genes.
The outcomes present excessive efficiency of the mannequin’s predictions, with an AUC of 0.89. 100 and twenty-one predicted pairs with excessive prediction scores have been chosen for inferring the features utilizing statistical enrichment evaluation. Utilizing this methodology, PF3D7_1248700 and PF3D7_0401800 have been discovered to be concerned with muscle contraction and striated muscle tissue improvement, whereas PF3D7_1303800 and PF3D7_1201000 have been discovered to be associated to protein dephosphorylation. In conclusion, combining a heterogeneous community and a hybrid deep studying approach can enable us to determine unknown gene features of malaria parasites. This method is generalized and will be utilized to different illnesses that improve the sphere of biomedical science.

 

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The impact of anionic polymers on gene delivery: how composition and assembly help evading the toxicity-efficiency dilemma
Cationic polymers have been broadly studied for non-viral gene supply on account of their means to bind genetic materials and to work together with mobile membranes. Nonetheless, their charged nature carries the danger of elevated cytotoxicity and interplay with serum proteins, limiting their potential in vivo utility. Due to this fact, hydrophilic or anionic shielding polymers are utilized to counteract these results. Herein, a sequence of micelle-forming and micelle-shielding polymers have been synthesized through RAFT polymerization.
The copolymer poly[(n-butyl acrylate)-b-(2-(dimethyl amino)ethyl acrylamide)] (P(nBA-b-DMAEAm)) was assembled into cationic micelles and totally different shielding polymers have been utilized, i.e., poly(acrylic acid) (PAA), poly(4-acryloyl morpholine) (PNAM) or P(NAM-b-AA) block copolymer. These techniques have been in comparison with a triblock terpolymer micelle comprising PAA as the center block. The assemblies have been investigated relating to their morphology, interplay with pDNA, cytotoxicity, transfection effectivity, polyplex uptake and endosomal escape.
The bare cationic micelle exhibited superior transfection effectivity, however elevated cytotoxicity. The addition of protecting polymers led to diminished toxicity. Particularly, the triblock terpolymer micelle satisfied with excessive cell viability and no important loss in effectivity. The very best shielding impact was achieved by layering micelles with P(NAM-b-AA) supporting the colloidal stability at impartial zeta potential and utterly restoring cell viability whereas sustaining reasonable transfection efficiencies. The excessive potential of this micelle-layer-combination for gene supply was illustrated for the primary time.

Genetic Evaluation, Inhabitants Construction, and Characterisation of Multidrug-Resistant Klebsiella pneumoniae from the Al-Hofuf Area of Saudi Arabia

Multidrug-resistant Klebsiella pneumoniae (MDR-KP) is a significant public well being drawback that’s globally related to illness outbreaks and excessive mortality charges. Because the world seeks options to such pathogens, international and regional surveillance is required. The goal of the current research was to look at the antimicrobial susceptibility sample and clonal relatedness of Klebsiella pneumoniae isolates collected for a interval of three years by way of pulse discipline gel electrophoresis (PFGE).
Isolate IDs, antimicrobial assays, ESBL-production, and minimal inhibitory concentrations (MICs) have been examined with the Vitek 2 Compact Automated System. IDs have been confirmed by 16S rRNA gene sequencing, with the ensuing sequences being deposited in NCBI databases. DNA was extracted and resistance genes have been detected by PCR amplification with applicable primers. Isolates have been intensive (31%) and multidrug-resistant (65%).
Pulsotype clusters grouped the isolates into 22 band profiles that confirmed no particular sample with phenotypes. Of the isolates, 98% have been ESBL-KP, 69% have been carbapenem-resistant Enterobacteriaceae (CRE) strains, and 72.5% comprised the carriage of two MBLs (SIM and IMP). Integrons (ISAba1, ISAba2, and IS18) have been detected in 69% of the MDR-KP. Moreover, OXA-23 was detected in 67% of the isolates. This research subsequently demonstrates clonal range amongst scientific Ok. pneumoniae, confirming that this bacterium has entry to an infinite pool of genes that confer excessive resistance-developing potential.

Full Genome Sequencing of Leptospira interrogans Isolates from Malaysia Reveals Large Genome Rearrangement however Excessive Conservation of Virulence-Related Genes

The power of Leptospirae to persist in environments and animal hosts however to trigger clinically extremely variable illness in people has made leptospirosis the most typical zoonotic illness. Contemplating the paucity of knowledge on variation in full genomes of human pathogenic Leptospirae, we’ve used a mix of Single Molecule Actual-Time (SMRT) and Illumina sequencing to acquire full genome sequences of six human scientific L. interrogans isolates from Malaysia.
  • All six contained the bigger (4.28-4.56 Mb) and smaller (0.34-0.395 Mb) chromosome typical of human pathogenic Leptospirae and 0-7 plasmids. Solely 24% of the plasmid sequences could possibly be matched to databases. We recognized a chromosomal core genome of 3318 coding sequences and strain-specific accent genomes of 49-179 coding sequences.
  • These sequences enabled detailed genomic pressure typing (Genome BLAST Distance Phylogeny, DNA-DNA hybridization, and multi locus sequence typing) and phylogenetic classification (whole-genome SNP genotyping). Regardless that there was some shared synteny and collinearity throughout the six genomes, there was proof of main genome rearrangement, doubtless pushed by horizontal gene switch and homologous recombination.
  • Cellular genetic parts have been recognized in all strains in extremely various numbers, together with within the rfb locus, which defines serogroups and contributes to immune escape and pathogenesis. Then again, there was excessive conservation of virulence-associated genes together with these referring to sialic acid, alginate, and lipid A biosynthesis.
  • These findings counsel (i) that the antigenic variation, adaption to numerous host environments, and broad spectrum of virulence of L. interrogans are partially on account of a excessive diploma of genomic plasticity and (ii) that human pathogenic strains keep a core set of genes required for virulence.
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Genomic Analyses of Penicillium Species Have Revealed Patulin and Citrinin Gene Clusters and Novel Loci Concerned in Oxylipin Manufacturing

Blue mildew of apple is attributable to a number of totally different Penicillium species, amongst which P. expansum and P. solitum are essentially the most ceaselessly remoted. P. expansum is essentially the most aggressive species, and P. solitum could be very weak when infecting apple fruit throughout storage. On this research, we report full genomic analyses of three totally different Penicillium species: P. expansum R21 and P. crustosum NJ1, remoted from saved apple fruit; and Pmaximae 113, remoted in 2013 from a flooded house in New Jersey, USA, within the aftermath of Hurricane Sandy. Patulin and citrinin gene cluster analyses defined the shortage of patulin manufacturing in NJ1 in comparison with R21 and lack of citrinin manufacturing in all three strains.
Drosophila bioassay demonstrated that volatiles emitted by Psolitum SA and Ppolonicum RS1 have been extra poisonous than these from Pexpansum and P. crustosum strains (R27, R11, R21, G10, and R19). The toxicity was hypothesized to be associated to manufacturing of eight-carbon oxylipins. Putative lipoxygenase genes have been recognized in Pexpansum and Pmaximae strains, however not in Pcrustosum. Our information will present a greater understanding of Penicillium spp. complicated secondary metabolic capabilities, particularly regarding the genetic bases of mycotoxins and poisonous VOCs.
Pig-to-human xenotransplantation appears to be the response to the up to date scarcity of tissue/organ donors. Sadly, the phylogenetic distance between pig and human implies hyperacute xenograft rejection. On this research, we examined the speculation that combining expression of human α1,2-fucosyltransferase (hFUT2) and α-galactosidase A (hGLA) genes would enable for removing of this impediment in porcine transgenic epidermal keratinocytes (PEKs). We sought to find out not solely the expression profiles of recombinant human α1,2-fucosyltransferase (rhα1,2-FT) and α-galactosidase A (rhα-Gal A) proteins, but in addition the relative abundance (RA) of Galα1→3Gal epitopes within the PEKs stemming from not solely hFUT2 or hGLA single-transgenic and hFUT2×hGLA double-transgenic pigs. Our confocal microscopy and Western blotting analyses revealed that each rhα1,2-FT and rhα-Gal A enzymes have been overabundantly expressed in respective transgenic PEK traces.
Furthermore, the semiquantitative ranges of Galα1→3Gal epitope that have been assessed by lectin fluorescence and lectin blotting have been discovered to be considerably diminished in every variant of genetically modified PEK line as in comparison with these noticed within the management nontransgenic PEKs. Notably, the bi-transgenic PEKs have been characterised by considerably lessened (however nonetheless detectable) RAs of Galα1→3Gal epitopes as in comparison with these recognized for each varieties of mono-transgenic PEK traces. Moreover, our present investigation confirmed that the coexpression of two protecting transgenes gave rise to enhanced abrogation of Galα→3Gal epitopes in hFUT2×hGLA double-transgenic PEKs.
To summarize, detailed estimation of semiquantitative profiles for human α-1,2-FT and α-Gal A proteins adopted by identification of the extent of abrogating the abundance of Galα1→3Gal epitopes within the ex vivo expanded PEKs stemming from mono- and bi-transgenic pigs have been discovered to be a sine qua non situation for effectively ex situ defending steady traces of skin-derived somatic cells inevitable in additional research.
The latter is because of be targeted on figuring out epigenomic reprogrammability of single- or double-transgenic cell nuclei inherited from grownup cutaneous keratinocytes in porcine nuclear-transferred oocytes and corresponding cloned embryos. To our data, this idea was proven to signify a very new strategy designed to generate and multiply genetically reworked pigs by somatic cell cloning for the wants of reconstructive drugs and dermoplasty-mediated tissue engineering of human integumentary system.
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Epigenetic and Genetic Integrity, Metabolic Stability, and Field Performance of Cryopreserved Plants
Cryopreservation is taken into account an excellent technique for the long-term preservation of plant genetic assets. Important progress was achieved over the previous a number of many years, ensuing within the profitable cryopreservation of the genetic assets of various plant species. Cryopreservation procedures typically make use of in vitro tradition methods and require the exact management of a number of steps, such because the excision of explants, preculture, osmo- and cryoprotection, dehydration, freeze-thaw cycle, unloading, and post-culture for the restoration of vegetation.
These processes create a worrying surroundings and trigger reactive oxygen species (ROS)-induced oxidative stress, which is detrimental to the expansion and regeneration of tissues and vegetation from cryopreserved tissues. ROS-induced oxidative stresses had been documented to induce (epi)genetic and somatic variations.
Subsequently, the event of true-to-type regenerants of the supply germplasm is of major concern within the utility of plant cryopreservation know-how. The current article supplies a complete evaluation of epigenetic and genetic integrity, metabolic stability, and discipline efficiency of cryopreserved vegetation developed prior to now decade. Potential areas and the instructions of future analysis in plant cryopreservation are additionally proposed.

Dosage-Dependent Gynoecium Improvement and Gene Expression in Brassica napus-Orychophragmus violaceus Addition Traces

Distant hybridization often results in feminine sterility of the hybrid however the mechanism behind that is poorly understood. Full pistil abortion however regular male fertility was proven by one Brassica napus-Orychophragmus violaceus monosomic alien addition line (MA, AACC + 1 IO, 2n = 39) produced beforehand. To review the impact of a single O. violaceus chromosome addition on pistil improvement in numerous genetic backgrounds, hybrids between the MA and B. carinata (BBCC), B. juncea (AABB), and two artificial hexaploids (AABBCC) had been firstly produced on this research which present full feminine sterility.
A microspore tradition was additional carried out to provide the haploid monosomic alien addition line (HMA, AC + 1 IO, 2n = 20) and disomic addition line (DA, AACC + 2 IO, 2n = 40) along with haploid (H, AC, 2n = 19) and double haploid (DH, AACC, 2n = 38) vegetation of B. napus from MA to analyze the dosage impact of the alien O. violaceus chromosome on pistil improvement and gene expression. In comparison with MA, the event of the pistils of DA and HMA was fully or partially recovered, wherein the pistils might swell and elongate to a traditional form after open pollination, though no seeds had been produced.
Comparative RNA-seq analyses revealed that the numbers of the differentially expressed genes (DEGs) had been considerably totally different, dosage-dependent, and in step with the phenotypic distinction in pairwise comparisons of HMA vs. H, DA vs. DH, MA vs. DH, MA vs. DA, and MA vs. HMA. The gene ontology (GO) enrichment evaluation of DEGs confirmed that a lot of genes concerned within the improvement of the gynoecium, embryo sac, ovule, and integuments. Significantly, a number of frequent DEGs for pistil improvement shared in HMA vs. H and DA vs. DH confirmed capabilities in genotoxic stress response, auxin transport, and signaling and adaxial/abaxial axis specification. The outcomes supplied up to date data for the molecular mechanisms behind the gynoecium improvement of B. napus responding to the dosage of alien O. violaceus chromosomes.

Courting the Frequent Ancestor from an NCBI Tree of 83688 Excessive-High quality and Full-Size SARS-CoV-2 Genomes

All relationship research involving SARS-CoV-2 are problematic. Earlier research have dated the latest frequent ancestor (MRCA) between SARS-CoV-2 and its shut kin from bats and pangolins. Nevertheless, the evolutionary price thus derived is predicted to vary from the speed estimated from sequence divergence of SARS-CoV-2 lineages. Right here, I current relationship outcomes for the primary time from a big phylogenetic tree with 86,582 high-quality full-length SARS-CoV-2 genomes.
  • The tree accommodates 83,688 genomes with full specification of assortment time. Such a big tree spanning a interval of about 1.5 years gives a superb alternative for relationship the MRCA of the sampled SARS-CoV-2 genomes. The MRCA is dated 16 August 2019, with the evolutionary price estimated to be 0.05526 mutations/genome/day.
  • The Pearson correlation coefficient (r) between the root-to-tip distance (D) and the gathering time (T) is 0.86295. The NCBI tree additionally consists of 10 SARS-CoV-2 genomes remoted from cats, collected over roughly the identical time span as human COVID-19 an infection.
  • The MRCA from these cat-derived SARS-CoV-2 is dated 30 July 2019, with r = 0.98464. Whereas the relationship technique is well-known, I’ve included detailed illustrations in order that anybody can repeat the evaluation and acquire the identical relationship outcomes.
  • With 16 August 2019 because the date of the MRCA of sampled SARS-CoV-2 genomes, archived samples from respiratory or digestive tracts collected round or earlier than 16 August 2019, or these that aren’t descendants of the prevailing SARS-CoV-2 lineages, must be significantly invaluable for tracing the origin of SARS-CoV-2.
hicstatistics
hicstatistics

Genome-Broad Identification of the HMA Gene Household and Expression Evaluation underneath Cd Stress in Barley

Lately, cadmium (Cd) air pollution in soil has elevated with growing industrial actions, which has restricted crop progress and agricultural improvement. The heavy metallic ATPase (HMA) gene household contributes to heavy metallic stress resistance in vegetation. On this research, 21 HMA genes (HvHMAs) had been recognized in barley (Hordeumvulgare L., Hv) utilizing bioinformatics strategies. Primarily based on phylogenetic evaluation and area distribution, barley HMA genes had been divided into 5 teams (A-E), and full analyses had been carried out by way of physicochemical properties, structural traits, conserved domains, and chromosome localization.
The expression sample evaluation confirmed that almost all HvHMA genes had been expressed in barley and exhibited tissue specificity. In response to the fragments per kilobase of exon per million fragments values in shoots from seedlings on the 10 cm shoot stage (LEA) and phylogenetic evaluation, 5 HvHMA genes had been chosen for expression evaluation underneath Cd stress. Among the many 5 HvHMA genes, three (HvHMA1HvHMA3, and HvHMA4) had been upregulated and two (HvHMA2 and HvHMA6) had been downregulated following Cd remedies. This research serves as a basis for clarifying the capabilities of HvHMA proteins within the heavy metallic stress resistance of barley.

Carbon Dioxide-Derived Biodegradable and Cationic Polycarbonates as a New siRNA Service for Gene Remedy in Pancreatic Most cancers

Pancreatic most cancers is an aggressive malignancy related to poor prognosis and a excessive tendency in growing infiltration and metastasis. Okay-ras mutation is a significant genetic dysfunction in pancreatic most cancers affected person. RNAi-based therapies may be employed for combating pancreatic most cancers by silencing Okay-ras gene expression. Nevertheless, the medical utility of RNAi know-how is appreciably restricted by the dearth of a correct siRNA supply system.
To deal with this hurdle, cationic poly (cyclohexene carbonate) s (CPCHCs) utilizing broadly sourced CO2 because the monomer are subtly synthesized through ring-opening copolymerization (ROCOP) and thiol-ene functionalization. The developed CPCHCs might successfully encapsulate therapeutic siRNA to kind CPCHC/siRNA nanoplexes (NPs). Serving as a siRNA service, CPCHC possesses biodegradability, negligible cytotoxicity, and excessive transfection effectivity. In vitro research exhibits that CPCHCs are able to successfully defending siRNA from being degraded by RNase and selling a sustained endosomal escape of siRNA.
After therapy with CPCHC/siRNA NPs, the Okay-ras gene expression in each pancreatic most cancers cell line (PANC-1 and MiaPaCa-2) are considerably down-regulated. Subsequently, the cell progress and migration are significantly inhibited, and the handled cells are induced into cell apoptotic program. These outcomes exhibit the promising potential of CPCHC-mediated siRNA therapies in pancreatic most cancers therapy.

 

hicstatistics
A Gene-Expression Predictor for Efficacy of Induction Chemotherapy in Locoregionally Advanced Nasopharyngeal Carcinoma

Background: Induction chemotherapy (IC) adopted by concurrent chemoradiotherapy is the mainstay therapy for sufferers with locoregionally superior nasopharyngeal carcinoma. Nonetheless, some sufferers acquire little profit and expertise pointless poisonousities from IC. We supposed to develop a gene-expression signature that may establish beneficiaries of IC.

 

Strategies: We screened chemosensitivity-related genes by evaluating gene-expression profiles of sufferers with short-term tumor response or nonresponse to IC (n = 95) utilizing microarray evaluation. Chemosensitivity-related genes had been quantified by digital expression profiling in a coaching cohort (n = 342) to acquire a gene signature. We then validated this gene signature within the scientific trial cohort (n = 187) and an exterior impartial cohort (n = 240). Assessments of statistical significance are 2-sided.

 

Outcomes: We recognized 43 chemosensitivity-related genes related to the short-term tumor response to IC. Within the coaching cohort, a 6-gene signature was developed that was extremely correct at predicting the short-term tumor response to IC (space below the curve [AUC] = 0.87, sensitivity = 87.5%, specificity = 75.6%).

We additional discovered that IC conferred failure-free survival advantages solely in sufferers within the profit group (hazard ratio [HR] = 0.54, 95% confidence interval [CI] = 0.34 to 0.87; P = .01) and never on these within the no-benefit group (HR = 1.25, 95% CI = 0.62 to 2.51; P = .53). Within the scientific trial cohort, the 6-gene signature was additionally extremely correct at predicting the tumor response (AUC = 0.82, sensitivity = 87.5%, specificity = 71.8%) and indicated failure-free survival advantages. Within the exterior impartial cohort, comparable outcomes had been noticed.

 

Conclusions: The 6-gene signature will help choose beneficiaries of IC and lay a basis for a extra individualized therapeutic technique for locoregionally superior nasopharyngeal carcinoma sufferers.

 

Genetic Occasions and Signaling Mechanisms Underlying Schwann Cell Destiny in Improvement and Most cancers

 

On this assessment, we describe Schwann cell improvement from embryonic neural crest cells to terminally differentiated myelinated and nonmyelinated mature Schwann cells. We deal with the genetic drivers and signaling mechanisms mediating choices to proliferate versus differentiate throughout Schwann cell improvement, highlighting pathways that overlap with Schwann cell improvement and are dysregulated in tumorigenesis.

We conclude by contemplating how our data of the occasions underlying Schwann cell improvement and mouse fashions of schwannoma, neurofibroma, and malignant peripheral nerve sheath tumor can inform novel therapeutic methods for sufferers with cancers derived from Schwann cell lineages.

The event and controversy of aggressive endogenous RNA speculation in non-coding genes

As a momentous post-transcriptional regulator, microRNAs (miRNAs) are attracting increasingly more consideration. The classical miRNAs regulated mechanism exhibits it binds to the targets’ 3’UTR thus play the function in post-transcription.

In the meantime, single miRNA can goal a number of genes, so these ought to compete to bind that miRNA. Vice versa, single gene can sponge mass of miRNAs as nicely. Thus the aggressive endogenous RNAs (ceRNAs) speculation was put ahead in 2011.

The ceRNA speculation has made big achievements, particularly in non-coding genes, which together with lengthy non-coding RNAs (lncRNAs), circle RNAs (circRNAs) and pseudogenes, even viral transcripts. It additionally contributed enormously to epigenetics improvement.

Nonetheless, an growing variety of controversies have occurred with applause. Primarily based on this example, this assessment introduces one thing in element in regards to the ceRNAs speculation achieved in lncRNAs,circRNAs, pseudogenes and viral transcripts, respectively. In the meantime, it additionally covers controversy of the ceRNAs speculation

hicstatistics
hicstatistics

Conserved Patterns in Developmental Processes and Phases, Somewhat than Genes, Unite the Extremely Divergent Bilateria 

  • Bilateria are the predominant clade of animals on Earth. Regardless of having developed all kinds of physique plans and developmental modes, they’re characterised by frequent morphological traits. By default, researchers have tried to hyperlink clade-particular genes to those traits, thus distinguishing bilaterians from non-bilaterians, by their gene content material.
  • Right here we argue that it’s relatively organic processes that unite Bilateria and set them aside from their non-bilaterian sisters, with a much less advanced physique morphology. To check this speculation, we in contrast proteomes of bilaterian and non-bilaterian species in an elaborate computational pipeline, aiming to seek for a set of bilaterian-specific genes. Regardless of the restricted confidence of their bilaterian specificity, we however detected Bilateria-specific practical and developmental patterns within the sub-set of genes conserved in distantly associated Bilateria.

 

  • Utilizing a novel multi-species GO-enrichment technique, we decided the practical repertoire of genes which might be extensively conserved amongst Bilateria. Analyzing expression profiles in three very distantly associated mannequin species- melanogasterD. rerioand C. elegans-we discover attribute peaks at comparable phases of improvement and a delayed onset of expression in embryos. Particularly, the expression of the conserved genes seems to peak on the phylotypic stage of various bilaterian phyla.

 

  • In abstract, our examine illustrate how improvement connects distantly associated Bilateria after thousands and thousands of years of divergence, pointing to processes doubtlessly separating them from non-bilaterians. We argue that evolutionary biologists ought to return from a purely gene-centric view of evolution and place extra deal with analyzing and defining conserved developmental processes and durations.

The efficacy of chemotherapeutic drug mixtures could also be predicted by concordance of gene response to the one brokers

Figuring out the expression of genes in response to completely different courses of chemotherapeutic medicine could permit for a greater understanding as to which can be used successfully together. Within the current examine, the human colorectal most cancers cell line HCT116 was cultured with equi-active concentrations of a sequence of anti-cancer brokers.

Gene expression profiles had been then measured by whole-genome microarray. Though every drug induced a singular signature of gene expression in tumour cells, there have been marked similarities between sure medicine, even in these from completely different courses. For instance, the antimalarial agent artesunate and the platinum-containing alkylating agent, oxaliplatin, produced a really comparable mRNA expression sample in HCT116 cells with ~14,000 genes being affected by the 2 medicine in the identical method.

Moreover, the general correlation of gene responses between two brokers may predict whether or not their use together would result in a higher or lesser impact on cell quantity, decided experimentally, than predicted by single agent experiments. The outcomes indicated that even when working by means of completely different mechanisms, combining medicine that provoke an identical transcriptional response could represent the most suitable choice for figuring out drug-combination methods for the therapy of most cancers.

 

Human Pim-3 Oncogene (PIM3) ELISA Kit

DLR-PIM3-Hu-96T 96T
EUR 725
  • Should the Human Pim-3 Oncogene (PIM3) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Pim-3 Oncogene (PIM3) in samples from serum, plasma, tissue homogenates or other biological fluids.

Human Pim-3 Oncogene (PIM3) ELISA Kit

RDR-PIM3-Hu-48Tests 48 Tests
EUR 589

Human Pim-3 Oncogene (PIM3) ELISA Kit

RDR-PIM3-Hu-96Tests 96 Tests
EUR 820

Human Pim-3 Oncogene (PIM3) ELISA Kit

RD-PIM3-Hu-48Tests 48 Tests
EUR 563

Human Pim-3 Oncogene (PIM3) ELISA Kit

RD-PIM3-Hu-96Tests 96 Tests
EUR 783

Pim-3 Oncogene (PIM3) Antibody

20-abx131576
  • EUR 453.00
  • EUR 133.00
  • EUR 1316.00
  • EUR 620.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-3 Oncogene (PIM3) Antibody

20-abx174068
  • EUR 926.00
  • EUR 467.00
  • 1 mg
  • 200 ug
  • Please enquire.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human)

4-PAN637Hu01
  • EUR 262.00
  • EUR 2747.00
  • EUR 679.00
  • EUR 331.00
  • EUR 220.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3)

Recombinant Pim-3 Oncogene (PIM3)

4-RPN637Hu01
  • EUR 467.36
  • EUR 228.00
  • EUR 1477.60
  • EUR 559.20
  • EUR 1018.40
  • EUR 376.00
  • EUR 3544.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
  • Uniprot ID: Q86V86
  • Buffer composition: PBS, pH 7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
  • Form: Freeze-dried powder
  • Predicted Molecular Mass (KD): 39.6kDa
  • Isoelectric Point: Inquire
Description: Recombinant Human Pim-3 Oncogene expressed in: E.coli

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), APC

4-PAN637Hu01-APC
  • EUR 368.00
  • EUR 3599.00
  • EUR 993.00
  • EUR 472.00
  • EUR 229.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with APC.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), Biotinylated

4-PAN637Hu01-Biotin
  • EUR 328.00
  • EUR 2697.00
  • EUR 786.00
  • EUR 404.00
  • EUR 226.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with Biotin.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), Cy3

4-PAN637Hu01-Cy3
  • EUR 449.00
  • EUR 4757.00
  • EUR 1283.00
  • EUR 588.00
  • EUR 264.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with Cy3.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), FITC

4-PAN637Hu01-FITC
  • EUR 314.00
  • EUR 2899.00
  • EUR 814.00
  • EUR 397.00
  • EUR 203.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with FITC.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), HRP

4-PAN637Hu01-HRP
  • EUR 335.00
  • EUR 3135.00
  • EUR 877.00
  • EUR 426.00
  • EUR 215.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with HRP.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), PE

4-PAN637Hu01-PE
  • EUR 314.00
  • EUR 2899.00
  • EUR 814.00
  • EUR 397.00
  • EUR 203.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with PE.

Human Pim-3 Oncogene (PIM3) Protein

20-abx650812
  • EUR 648.00
  • EUR 272.00
  • EUR 1998.00
  • EUR 773.00
  • EUR 467.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-3 Oncogene (PIM3) Polyclonal Antibody (Human), APC-Cy7

4-PAN637Hu01-APC-Cy7
  • EUR 616.00
  • EUR 7078.00
  • EUR 1867.00
  • EUR 824.00
  • EUR 338.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM3 (Met1~Leu326)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-3 Oncogene (PIM3). This antibody is labeled with APC-Cy7.

Human Pim-3 Oncogene (PIM3)ELISA Kit

201-12-2347 96 tests
EUR 440
  • This Pim-3 Oncogene ELISA kit is validated to work with samples from whole blood, serum, plasma and cell culture supernatant.
Description: A quantitative ELISA kit for measuring Human in samples from biological fluids.

Human Pim-3 Oncogene (PIM3) CLIA Kit

20-abx190020
  • EUR 7911.00
  • EUR 4215.00
  • EUR 973.00
  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests
  • Shipped within 5-7 working days.

Human Pim-3 Oncogene (PIM3) ELISA Kit

20-abx152746
  • EUR 7378.00
  • EUR 3933.00
  • EUR 911.00
  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests
  • Shipped within 5-7 working days.

Human Pim-3 Oncogene(PIM3)ELISA Kit

QY-E04696 96T
EUR 361

Rat Pim-3 Oncogene(PIM3)ELISA Kit

QY-E10537 96T
EUR 400

Human Pim-3 Oncogene (PIM3)CLIA Kit

SCN637Hu-10x96wellstestplate 10x96-wells test plate
EUR 5647.8
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-3 Oncogene (PIM3) in tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3)CLIA Kit

SCN637Hu-1x48wellstestplate 1x48-wells test plate
EUR 552.76
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-3 Oncogene (PIM3) in tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3)CLIA Kit

SCN637Hu-1x96wellstestplate 1x96-wells test plate
EUR 746.8
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-3 Oncogene (PIM3) in tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3)CLIA Kit

SCN637Hu-5x96wellstestplate 5x96-wells test plate
EUR 3060.6
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-3 Oncogene (PIM3) in tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3) CLIA Kit

4-SCN637Hu
  • EUR 5698.00
  • EUR 3061.00
  • EUR 747.00
  • 10 plates of 96 wells
  • 5 plates of 96 wells
  • 1 plate of 96 wells
  • Known also as Pim-3 Oncogene Clia kit. Alternative names of the recognized antigen: Serine/threonine-protein kinase pim-3
Description: Double-antibody Sandwich chemiluminescent immunoassay for detection of Human Pim-3 Oncogene (PIM3)tissue homogenates and other biological fluids

Mouse Pim-3 Oncogene(PIM3)ELISA Kit

QY-E21186 96T
EUR 361

Human Pim-3 Oncogene (PIM3) ELISA Kit

SEN637Hu-10x96wellstestplate 10x96-wells test plate
EUR 5189.65
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Pim-3 Oncogene (PIM3) in serum, plasma, tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3) ELISA Kit

SEN637Hu-1x48wellstestplate 1x48-wells test plate
EUR 515.03
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Pim-3 Oncogene (PIM3) in serum, plasma, tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3) ELISA Kit

SEN637Hu-1x96wellstestplate 1x96-wells test plate
EUR 692.9
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Pim-3 Oncogene (PIM3) in serum, plasma, tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3) ELISA Kit

SEN637Hu-5x96wellstestplate 5x96-wells test plate
EUR 2818.05
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-3 Oncogene (PIM3) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Pim-3 Oncogene (PIM3) in serum, plasma, tissue homogenates and other biological fluids.

Human Pim-3 Oncogene (PIM3) ELISA Kit

4-SEN637Hu
  • EUR 5240.00
  • EUR 2769.00
  • EUR 693.00
  • 10 plates of 96 wells
  • 5 plates of 96 wells
  • 1 plate of 96 wells
  • Known also as Pim-3 Oncogene elisa. Alternative names of the recognized antigen: Serine/threonine-protein kinase pim-3
Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Human Pim-3 Oncogene (PIM3) in samples from serum, plasma, tissue homogenates and other biological fluids with no significant corss-reactivity with analogues from other species.

ELISA kit for Human PIM3 (Pim-3 Oncogene)

ELK6491 1 plate of 96 wells
EUR 432
  • The microtiter plate provided in this kit has been pre-coated with an antibody specific to Pim-3 Oncogene (PIM3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Pim-3 Oncoge
  • Show more
Description: A sandwich ELISA kit for detection of Pim-3 Oncogene from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Rabbit Polyclonal antibody Anti-CRBN

Anti-CRBN 50 µg
EUR 349

Polyclonal Goat anti-GST p-form

GST-ANTI-3 50 uL
EUR 280

Serine/Threonine-Protein Kinase Pim-3 (PIM3) Antibody

20-abx214125
  • EUR 411.00
  • EUR 300.00
  • 100 ul
  • 50 ul
  • Shipped within 5-10 working days.

Serine/Threonine-Protein Kinase Pim-3 (PIM3) Antibody

20-abx241699
  • EUR 411.00
  • EUR 300.00
  • 100 ul
  • 50 ul
  • Shipped within 5-10 working days.

Serine/threonine-Protein Kinase Pim-3 (PIM3) Antibody

20-abx318212
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug
  • Shipped within 5-10 working days.

Rabbit Pim 1 Oncogene ELISA kit

E04P0753-192T 192 tests
EUR 1270
  • Kit contents: 1. MICROTITER PLATE * 1 2. ENZYME CONJUGATE*1 vial 3. STANDARD A*1 vial 4. STANDARD B*1 vial 5. STANDARD C*1 vial 6. STANDARD D*1 vial 7. STANDARD E*1 vial 8. STANDARD F*1 vial 9. SUBSTRATE A*1 vial 10. SUBSTRATE B*1 vial 11. STOP SOLUT
  • Show more
Description: A competitive ELISA for quantitative measurement of Rabbit Pim 1 Oncogene in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Rabbit Pim 1 Oncogene ELISA kit

E04P0753-48 1 plate of 48 wells
EUR 520
  • Kit contents: 1. MICROTITER PLATE * 1 2. ENZYME CONJUGATE*1 vial 3. STANDARD A*1 vial 4. STANDARD B*1 vial 5. STANDARD C*1 vial 6. STANDARD D*1 vial 7. STANDARD E*1 vial 8. STANDARD F*1 vial 9. SUBSTRATE A*1 vial 10. SUBSTRATE B*1 vial 11. STOP SOLUT
  • Show more
Description: A competitive ELISA for quantitative measurement of Rabbit Pim 1 Oncogene in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Rabbit Pim 1 Oncogene ELISA kit

E04P0753-96 1 plate of 96 wells
EUR 685
  • Kit contents: 1. MICROTITER PLATE * 1 2. ENZYME CONJUGATE*1 vial 3. STANDARD A*1 vial 4. STANDARD B*1 vial 5. STANDARD C*1 vial 6. STANDARD D*1 vial 7. STANDARD E*1 vial 8. STANDARD F*1 vial 9. SUBSTRATE A*1 vial 10. SUBSTRATE B*1 vial 11. STOP SOLUT
  • Show more
Description: A competitive ELISA for quantitative measurement of Rabbit Pim 1 Oncogene in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Serine/threonine-Protein Kinase Pim-3 (PIM3) Antibody (HRP)

20-abx315070
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug
  • Shipped within 5-10 working days.

Serine/threonine-Protein Kinase Pim-3 (PIM3) Antibody (FITC)

20-abx315071
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug
  • Shipped within 5-10 working days.

Serine/threonine-Protein Kinase Pim-3 (PIM3) Antibody (Biotin)

20-abx315072
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug
  • Shipped within 5-10 working days.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse)

4-PAC578Mu01
  • EUR 251.00
  • EUR 2576.00
  • EUR 640.00
  • EUR 316.00
  • EUR 215.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1)

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat)

4-PAC578Ra01
  • EUR 259.00
  • EUR 2708.00
  • EUR 670.00
  • EUR 328.00
  • EUR 219.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1)

Pim-2 Oncogene (PIM2) Polyclonal Antibody (Human)

4-PAP797Hu01
  • EUR 262.00
  • EUR 2747.00
  • EUR 679.00
  • EUR 331.00
  • EUR 220.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM2 (Leu82~Glu291)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human Pim-2 Oncogene (PIM2)

Pim-2 Oncogene (PIM2) Polyclonal Antibody (Mouse)

4-PAP797Mu01
  • EUR 266.00
  • EUR 2813.00
  • EUR 694.00
  • EUR 337.00
  • EUR 222.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM2 (Gly98~Cys319)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-2 Oncogene (PIM2)

Pim-2 Oncogene (PIM2) Polyclonal Antibody (Rat)

4-PAP797Ra01
  • EUR 275.00
  • EUR 2958.00
  • EUR 727.00
  • EUR 350.00
  • EUR 226.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM2 (Leu34~Glu292)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-2 Oncogene (PIM2)

Pim-1 Oncogene (PIM1) Antibody

20-abx101233
  • EUR 425.00
  • EUR 133.00
  • EUR 1205.00
  • EUR 578.00
  • EUR 328.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-1 Oncogene (PIM1) Antibody

20-abx101234
  • EUR 439.00
  • EUR 133.00
  • EUR 1233.00
  • EUR 592.00
  • EUR 328.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-1 Oncogene (PIM1) Antibody

20-abx101235
  • EUR 453.00
  • EUR 133.00
  • EUR 1302.00
  • EUR 620.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-12 working days.

Pim-2 Oncogene (PIM2) Antibody

20-abx101236
  • EUR 467.00
  • EUR 133.00
  • EUR 1344.00
  • EUR 634.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-2 Oncogene (PIM2) Antibody

20-abx101237
  • EUR 481.00
  • EUR 133.00
  • EUR 1414.00
  • EUR 662.00
  • EUR 356.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-2 Oncogene (PIM2) Antibody

20-abx129066
  • EUR 453.00
  • EUR 133.00
  • EUR 1316.00
  • EUR 620.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.

Pim-1 Oncogene (PIM1) Antibody

abx146417-100ug 100 ug
EUR 391
  • Shipped within 5-10 working days.

Pim-1 Oncogene (PIM1) Antibody

20-abx174066
  • EUR 857.00
  • EUR 439.00
  • 1 mg
  • 200 ug
  • Please enquire.

Pim-2 Oncogene (PIM2) Antibody

20-abx174067
  • EUR 926.00
  • EUR 467.00
  • 1 mg
  • 200 ug
  • Please enquire.

Pim-2 Oncogene (PIM2) Antibody

abx236456-100ug 100 ug
EUR 551
  • Shipped within 5-12 working days.

Pim-2 Oncogene (PIM2) Antibody

abx431508-200ul 200 ul
EUR 384
  • Shipped within 1-3 working days.

Pim-2 Oncogene (PIM2) Antibody

abx433133-200ul 200 ul
EUR 384
  • Shipped within 1-3 working days.

Pim-2 Oncogene (PIM2) Antibody

abx433134-200ul 200 ul
EUR 384
  • Shipped within 1-3 working days.

Anti-PIM3 antibody

STJ119424 100 µl
EUR 277
Description: The protein encoded by this gene belongs to the Ser/Thr protein kinase family, and PIM subfamily. This gene is overexpressed in hematological and epithelial tumors and is associated with MYC coexpression. It plays a role in the regulation of signal transduction cascades, contributing to both cell proliferation and survival, and provides a selective advantage in tumorigenesis.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), APC

4-PAC578Mu01-APC
  • EUR 351.00
  • EUR 3365.00
  • EUR 935.00
  • EUR 449.00
  • EUR 222.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with APC.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), Biotinylated

4-PAC578Mu01-Biotin
  • EUR 316.00
  • EUR 2526.00
  • EUR 744.00
  • EUR 387.00
  • EUR 221.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with Biotin.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), Cy3

4-PAC578Mu01-Cy3
  • EUR 427.00
  • EUR 4445.00
  • EUR 1205.00
  • EUR 557.00
  • EUR 254.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with Cy3.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), FITC

4-PAC578Mu01-FITC
  • EUR 301.00
  • EUR 2712.00
  • EUR 768.00
  • EUR 379.00
  • EUR 197.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with FITC.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), HRP

4-PAC578Mu01-HRP
  • EUR 321.00
  • EUR 2933.00
  • EUR 827.00
  • EUR 405.00
  • EUR 209.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with HRP.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), PE

4-PAC578Mu01-PE
  • EUR 301.00
  • EUR 2712.00
  • EUR 768.00
  • EUR 379.00
  • EUR 197.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with PE.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), APC

4-PAC578Ra01-APC
  • EUR 364.00
  • EUR 3545.00
  • EUR 980.00
  • EUR 467.00
  • EUR 227.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with APC.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), Biotinylated

4-PAC578Ra01-Biotin
  • EUR 325.00
  • EUR 2658.00
  • EUR 777.00
  • EUR 400.00
  • EUR 225.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with Biotin.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), Cy3

4-PAC578Ra01-Cy3
  • EUR 444.00
  • EUR 4685.00
  • EUR 1265.00
  • EUR 581.00
  • EUR 261.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with Cy3.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), FITC

4-PAC578Ra01-FITC
  • EUR 311.00
  • EUR 2856.00
  • EUR 804.00
  • EUR 393.00
  • EUR 202.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with FITC.

Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), HRP

4-PAC578Ra01-HRP
  • EUR 332.00
  • EUR 3089.00
  • EUR 866.00
  • EUR 421.00
  • EUR 213.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with HRP.
hicstatistics
The Genetic Diversification of a Single Bluetongue Virus Strain Using an In Vitro Model of Alternating-Host Transmission

Bluetongue virus (BTV) is an arbovirus that has been related to dramatic epizootics in each wild and residential ruminants in latest a really very long time. As a segmented, double-stranded RNA virus, BTV can evolve by a number of mechanisms because of its genomic constructing. Nonetheless, the have an effect on of BTV’s alternating-host transmission cycle on the virus’s genetic diversification stays poorly understood. Full genome sequencing approaches present a platform for investigating the have an effect on of host-alternation all by all ten segments of BTV’s genome.

 

To grasp the function of alternating hosts in BTV’s genetic diversification, a subject isolate was passaged beneath three totally completely completely different situations: (i) serial passages in Culicoidessonorensis cells, (ii) serial passages in bovine pulmonary artery endothelial cells, or (iii) alternating passages between insect and bovine cells.

 

Aliquots of virus had been sequenced, and single nucleotide variants had been acknowledged. Measures of viral inhabitants genetics had been used to quantify the genetic diversification that occurred. Two consensus variants in segments 5 and 10 occurred in virus from all three situations.

 

Whereas variants arose all by all passages, measures of genetic differ remained largely comparable all by cell customized situations. Irrespective of passage in a relaxed in vitro system, we discovered that this BTV isolate exhibited genetic stability all by passages and situations. Our findings underscore the expensive function that full genome sequencing could play in enhancing understanding of viral evolution and spotlight the genetic stability of BTV.

Novel Gene Rearrangement and the Full Mitochondrial Genome of Cynoglossusmonopus: Insights into the Envolution of the Household Cynoglossidae (Pleuronectiformes)

 

Cynoglossusmonopus, a small benthic fish, belongs to the Cynoglossidae, Pleuronectiformes. It was not normally studied because of its low abundance and cryptical life-style. With the intention to know the mitochondrial genome and the phylogeny in Cynoglossidae, all of the mitogenome of C. monopus has been sequenced and analyzed for the primary time. The entire dimension is 16,425 bp, usually containing 37 genes with novel gene rearrangements. The tRNA-Gln gene is inverted from the sunshine to the heavy strand and translocated from the downstream of tRNA-Ile gene to its upstream. The administration area (CR) translocated downstream to the three’-end of ND1 gene adjoining to inverted to tRNA-Gln and left a 24 bp hint fragment inside the real place.

 

 

The phylogenetic timber had been reconstructed by Bayesian inference (BI) and most likelihood (ML) strategies based completely on the mitogenomic data of 32 tonguefish species and two outgroups. The outcomes help the concept Cynoglossidae is a monophyletic group and degree out that C. monopus has the closest phylogenetic relationship with C. puncticeps.

 

By combining fossil data and mitogenome data, the time-calibrated evolutionary tree of households Cynoglossidae and Soleidae was firstly supplied, and it was indicated that Cynoglossidae and Soleidae had been differentiated from one another all by Paleogene, and the evolutionary technique of household Cynoglossidae coated the Quaternary, Neogene and Paleogene durations.

 

Genome-Broad Identification and Characterization of the SHI-Associated Sequence Gene Household in Rice

 

Rice (Oryzasativa) yield is correlated to varied elements. Transcription regulators are necessary elements, akin to the frequently SHORT INTERNODES-related sequences (SRSs), which encode proteins with single zinc finger motifs. Nonetheless, data relating to the evolutionary and smart traits of the SRS gene household members in rice is inadequate.

 

Subsequently, we carried out a genome-wide screening and characterization of the OsSRS gene household in Oryzasativa japonica rice. We furthermore examined the SRS proteins from 11 rice sub-species, consisting of three cultivars, 6 wild varieties, and some completely completely different genome sorts. SRS members from maize, sorghum, Brachypodiumdistachyon, and Arabidopsis had been furthermore investigated.

 

All these SRS proteins exhibited species-specific traits, together with monocot- and dicot-specific traits, as assessed by phylogenetic evaluation, which was additional validated by gene constructing and motif analyses. Genome comparisons revealed that segmental duplications may have carried out crucial roles contained in the recombination of the OsSRS gene household and their expression ranges. The household was primarily subjected to purifying selective stress.

 

Along with, the expression data demonstrated the distinct responses of OsSRS genes to varied abiotic stresses and hormonal cures, indicating their smart divergence. Our research gives an exquisite reference for elucidating the choices of SRS genes in rice.

 

hicstatistics
hicstatistics

Ginsenoside Rg1 improves pathological damages by activating the p21‑p53‑STK pathway in ovary and Bax‑Bcl2 within the uterus in untimely ovarian insufficiency mouse fashions

The intention of the current research was to research the results of the ginsenoside Rg1 on D‑galactose (D‑gal)‑induced mouse fashions of untimely ovarian insufficiency (POI) and the associated mechanisms. C57BL/6 feminine mice had been randomly grouped into the next: i) D‑gal [subcutaneously (s.c.) 200 mg/kg/d D‑gal for 42 days]; ii) Rg1 [intraperitoneally (i.p.) 20 mg/kg/d Rg1 for 28 days]; iii) D‑gal + Rg1 (s.c. 200 mg/kg/d D‑gal for 42 days adopted by i.p. 20 mg/kg/d Rg1 for 28 days); and iv) saline teams (equal quantity of saline s.c. and that i.p.). Hematoxylin and eosin staining and electron microscopy had been used to research uterine and ovarian morphology.
Expression ranges of senescence components (p21, p53 and serine/threonine kinase), secretion of professional‑inflammatory cytokines [interleukin (IL)‑6, tumor necrosis factor (TNF)‑α and IL‑1β] and the actions of oxidation biomarkers [superoxide dismutase (T‑SOD), malondialdehyde (MDA) and glutathione peroxidase (GSH‑px)] had been analyzed. The outcomes confirmed that mice within the Rg1 + D‑gal group had considerably larger uterine and ovarian weight in contrast with these within the D‑gal group.
Uterus morphology was additionally improved, primarily based on the comparability between the D‑gal group and the Rg1 + D‑gal group. As well as, the Rg1 remedy after D‑gal administration considerably decreased the expression of senescence‑related components, enhanced the actions of anti‑oxidant enzymes complete T‑SOD and GSH‑px along with decreasing TNF‑α, IL‑1β, MDA and IL‑6 (primarily based on the comparability between the D‑gal group and the Rg1 + D‑gal group).
In conclusion, the current research advised that the ginsenoside Rg1 improved pathological damages within the ovary and uterus by rising anti‑oxidant and anti‑inflammatory talents while decreasing the expression of senescence signaling pathways in POI mouse fashions.

 

 

PP1 (Src kinase inhibitor)

SIH-469-25MG 25 mg
EUR 619
  • PP1 is a potent and selective Src family protein tyrosine kinase inhibitor. This has a range of effects and implications. Structural studies have revealed that PP1 binds to the ATP-binding site in tyrosine kinases and Ser/Thr kinases. PP1 displays >
  • Show more
Description: The substance PP1 is a src kinase inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is tan solid which is soluble in DMSO (25 mg/ml), slightly soluble in 100% ethanol.

PP1 (Src kinase inhibitor)

SIH-469-5MG 5 mg
EUR 205
  • PP1 is a potent and selective Src family protein tyrosine kinase inhibitor. This has a range of effects and implications. Structural studies have revealed that PP1 binds to the ATP-binding site in tyrosine kinases and Ser/Thr kinases. PP1 displays >
  • Show more
Description: The substance PP1 is a src kinase inhibitor. It is synthetically produced and has a purity of >98%. The pure substance is tan solid which is soluble in DMSO (25 mg/ml), slightly soluble in 100% ethanol.

PP2 (Src kinase inhibitor)

SIH-470-25MG 25 mg
EUR 737
  • PP2 is a selective inhibitor of Src-family tyrosine kinases. PP2 has been shown to inhibit Lck, FynT, and phosphorylation of focal adhesion kinase (FAK) and potently inhibits Hck, Lck (p56) and Fyn (p59). PP2 displays > 10000-fold selectivity over ZA
  • Show more
Description: The substance PP2 is a src kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (25 mg/ml).

PP2 (Src kinase inhibitor)

SIH-470-5MG 5 mg
EUR 233
  • PP2 is a selective inhibitor of Src-family tyrosine kinases. PP2 has been shown to inhibit Lck, FynT, and phosphorylation of focal adhesion kinase (FAK) and potently inhibits Hck, Lck (p56) and Fyn (p59). PP2 displays > 10000-fold selectivity over ZA
  • Show more
Description: The substance PP2 is a src kinase inhibitor. It is synthetically produced and has a purity of ?98%. The pure substance is off-white solid which is soluble in DMSO (25 mg/ml).

SRC kinase signaling inhibitor 1 (SRCIN1) Antibody

abx331175-100ul 100 ul
EUR 425
  • Shipped within 5-10 working days.

SRC kinase signaling inhibitor 1 (SRCIN1) Antibody

20-abx327632
  • EUR 314.00
  • EUR 244.00
  • 100 ug
  • 50 ug
  • Shipped within 5-10 working days.

HPGDS inhibitor 1

B1046-1 1 mg
EUR 181
Description: HPGDS inhibitor 1 is an oral potent and selective inhibitor of hematopoietic prostaglandin D synthase (HPGDS) with IC50 value of 0.7nM [1].Prostaglandin D2 (PGD2) is a mediator of allergy and inflammation.

Anti-Src Rabbit Monoclonal Antibody

M00107-1 100ug/vial
EUR 397
Description: Rabbit Monoclonal Src Antibody. Validated in IF, WB and tested in Human, Rat.

Human SRC kinase signaling inhibitor 1, SRCIN1 ELISA KIT

ELI-13954h 96 Tests
EUR 824

Mouse SRC kinase signaling inhibitor 1, Srcin1 ELISA KIT

ELI-18126m 96 Tests
EUR 865

Rat SRC kinase signaling inhibitor 1 (SRCIN1) ELISA Kit

abx392007-96tests 96 tests
EUR 911
  • Shipped within 5-12 working days.

Human SRC kinase signaling inhibitor 1 (SRCIN1) ELISA Kit

abx385443-96tests 96 tests
EUR 911
  • Shipped within 5-12 working days.

Mouse SRC kinase signaling inhibitor 1 (SRCIN1) ELISA Kit

abx390644-96tests 96 tests
EUR 911
  • Shipped within 5-12 working days.

pp60 c-src (521-533) (phosphorylated)

B5235-1 1 mg
EUR 266

SRC 1 Antibody

abx238217-100ug 100 ug
EUR 509
  • Shipped within 5-12 working days.

187-1, N-WASP inhibitor

B5251-1 1 mg
EUR 399

Srcin1 ELISA Kit| Mouse SRC kinase signaling inhibitor 1 ELISA

EF016287 96 Tests
EUR 689

YAP-TEAD Inhibitor 1 (Peptide 17)

A1149-1 1 mg
EUR 235

SRC - 1 (682–697)

5-01959 4 x 1mg Ask for price

SRC-1 (pT1179) Antibody

abx217070-100ug 100 ug
EUR 439
  • Shipped within 5-10 working days.

anti- SRC 1 antibody

FNab08217 100µg
EUR 548.75
  • Recommended dilution: WB: 1:500-1:5000IHC: 1:20-1:200
  • Immunogen: nuclear receptor coactivator 1
  • Uniprot ID: Q15788
  • Gene ID: 8648
  • Research Area: Signal Transduction, Metabolism
Description: Antibody raised against SRC 1

T338C Src-IN-1

HY-16905 100mg
EUR 2943

Anti-SRC 1 antibody

PAab08217 100 ug
EUR 386

Srcin1 ELISA Kit| Rat SRC kinase signaling inhibitor 1 ELISA Ki

EF019367 96 Tests
EUR 689

Chk2 Inhibitor

1702-1
EUR 180

SCD1 Inhibitor

1716-1
EUR 218

ACC2 Inhibitor

1717-1
EUR 218

Syk Inhibitor

1983-1
EUR 126

Stat5 Inhibitor

9484-1
EUR 120

EGFR Inhibitor

C3327-1 1 mg
EUR 154
Description: EGFR inhibitor is a cell permeable, pyrimidine compound that selectively inhibits the EGFR kinase with IC50 value of 21 nM [1]. EGFR is a transmembrane protein, and is a receptor for members of epidermal growth factor family.

Lck Inhibitor

A3539-1 1 mg
EUR 154
Description: Lck Inhibitor is a small-molecule inhibitor of with IC50 value of 7 nM [1].The lymphocyte specific kinase which expressed in NK cells and T-cells is a member of the Src kinase family.

NFAT Inhibitor

A4539-1 1 mg
EUR 138
Description: Selective inhibitor of calcineurin-mediated dephosphorylation of nuclear factor of activated T cells (NFAT). Does not disrupt other calcineurin-dependent pathways. Inhibits NFAT activation and NFAT-dependent expression of endogenous cytokine genes in T cells.

c-SRC (c-SRC) Antibody

20-abx007517
  • EUR 300.00
  • EUR 439.00
  • EUR 189.00
  • 100 ul
  • 200 ul
  • 30 ul
  • Shipped within 5-10 working days.

c-SRC (c-SRC) Antibody

20-abx008688
  • EUR 300.00
  • EUR 439.00
  • EUR 189.00
  • 100 ul
  • 200 ul
  • 30 ul
  • Shipped within 5-10 working days.

Src/ Rat Src ELISA Kit

ELI-18125r 96 Tests
EUR 886

c-SRC (c-SRC) Antibody

abx232027-100ug 100 ug
EUR 551
  • Shipped within 5-12 working days.

c-SRC (c-SRC) Antibody

abx232028-100ug 100 ug
EUR 551
  • Shipped within 5-12 working days.

Phosphatase Inhibitor Cocktail 1 (100X in DMSO)

K1012-1 1 ml
EUR 102

NCOA1/SRC-1/KAT13A/ Rat NCOA1/ SRC- 1/ KAT13A ELISA Kit

ELA-E11292r 96 Tests
EUR 886

Human Plasminogen Activator Inhibitor-1 (PAI-1) AssayMax ELISA Kit

EP1100-1 96 Well Plate
EUR 417

SERPINE1 Plasminogen Activator Inhibitor-1 Human Recombinant Protein

PROTP05121-1 Regular: 25ug
EUR 317
Description: SERPINE1 Human Recombinant fused to N-terminal His-Tag produced in E.Coli is a single, non-glycosylated polypeptide chain containing 400 amino acids (24-402) and having a molecular mass of 45 kDa.;The SERPINE1 is purified by proprietary chromatographic techniques.

Bromodomain Inhibitor, (+)-JQ1

2070-1
EUR 164

Smad3 Inhibitor, SIS3

2227-1
EUR 164

CFTR Inhibitor-172

2487-1
EUR 120

EZSolution? SCD1 Inhibitor

2548-1
EUR 207

FAS Inhibitor, C75

1547-1
EUR 180

Batimastat (MMP Inhibitor)

1704-1
EUR 180

Cathepsin G Inhibitor

1982-1
EUR 240

USP7/USP47 Inhibitor

B2538-1
EUR 142

Cdk9 Inhibitor II

B2903-1
EUR 142

MLCK inhibitor peptide

B5236-1 1 mg
EUR 184

Rac1 Inhibitor W56

B5274-1 1 mg
EUR 399

Lyn peptide inhibitor

B5285-1 1 mg
EUR 601

Calpain Inhibitor XII

C5347-1 1 mg
EUR 145
Description: Ki: 19 nM for ?-calpain Calpain Inhibitor XII is a reversible and selective inhibitor of calpain I.Calpain is a protein belonging to the family of calcium-dependent, non-lysosomal cysteine proteases expressed ubiquitously in mammals and many other organisms.

MMP-13 Inhibitor

C4331-1 1 mg
EUR 187
Description: IC50: 8 nMMMP-13 Inhibitor is a MMP-13 inhibitor.Matrix metalloproteinases (MMPs), a family of zinc endopeptidases, can degrade proteins of the extracellular matrix, such as collagens, elastins, matrix glycoproteins, and proteoclycans.

EGFR/ErbB2 Inhibitor

C3285-1 1 mg
EUR 186
Description: IC50: 20 and 79 nM for EGFR and c-ErbB2, respectivelyEGFR/ErbB2 Inhibitor is an EGFR and c-ErbB2 inhibitor.EGFR and c-ErbB-2 are members of the epidermal growth factor receptor subfamily of protein tyrosine kinases.

MMP Inhibitor II

C4081-1 1 mg
EUR 119
Description: MMP Inhibitor II is a potent, reversible and broad-range inhibitor of matrix metalloproteinases (MMPs) with IC50 values of 24 nM, 18.4 nM, 30 nM and 2.7 nM for MMP-1, MMP-3, MMP-7 and MMP-9, respectively [1].

MEK Inhibitor Set

A9907-1 1 Set
EUR 224

Bromodomain Inhibitor, (+)-JQ1

A1910-1 1 mg
EUR 108
Description: Bromodomain Inhibitor, (+)-JQ1 is a potent and highly specific inhibitor for the BET (bromodomain and extra-terminal) family of bromodomains. (+)-JQ1 binds to BRD4 bromodomains 1 and 2 with Kd values of ~ 50 and 90 nM, respectively.

DiscoveryProbe? Inhibitor Library

L1048-.1 100 uL/well(10 mM solution)
EUR 14387

Plasminogen Activator Inhibitor 1 (PAI-1), hexapeptide, Human

SP-55196-1 0.5 mg
EUR 141

Src antibody

20R-2005 50 ug
EUR 281
Description: Rabbit polyclonal Src antibody

Src antibody

20R-2336 50 ug
EUR 281
Description: Rabbit polyclonal Src antibody

SRC antibody

70R-20514 50 ul
EUR 435
Description: Rabbit polyclonal SRC antibody

Src antibody

70R-13956 100 ug
EUR 322
Description: Affinity purified Rabbit polyclonal Src antibody

SRC Antibody

48186-100ul 100ul
EUR 333

SRC Antibody

48186-50ul 50ul
EUR 239

SRC Antibody

35933-100ul 100ul
EUR 252

SRC antibody

10R-2138 100 ul
EUR 457
Description: Mouse monoclonal SRC antibody

SRC antibody

10R-2154 100 ul
EUR 435
Description: Mouse monoclonal SRC antibody

Src antibody

10R-8485 100 ul
EUR 393
Description: Mouse monoclonal Src antibody

RR-SRC

5-01886 4 x 5mg Ask for price

Src Antibody

48902-100ul 100ul
EUR 333

Src Antibody

48902-50ul 50ul
EUR 239

Src Antibody

49317-100ul 100ul
EUR 333

Src Antibody

49317-50ul 50ul
EUR 239

SRC Antibody

1-CSB-PA001803
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
  • Form: Liquid
  • Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, IF, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.IF:1/200-1/1000.ELISA:1/40000

SRC Antibody

1-CSB-PA001806
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
  • Form: Liquid
  • Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/20000

SRC Antibody

1-CSB-PA001807
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
  • Form: Liquid
  • Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.ELISA:1/10000

SRC Antibody

1-CSB-PA001809
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
  • Form: Liquid
  • Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, IHC, ELISA;WB:1/500-1/2000.IHC:1/100-1/300.ELISA:1/5000

SRC Antibody

1-CSB-PA050134
  • EUR 222.00
  • EUR 195.00
  • 100ug
  • 50ug
  • Form: Liquid
  • Buffer: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/5000

SRC Antibody

1-CSB-PA080378
  • EUR 317.00
  • EUR 244.00
  • 100ul
  • 50ul
  • Form: Liquid
  • Buffer: -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Antigen affinity purification
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:25-1:100

SRC Antibody

1-CSB-PA081645
  • EUR 317.00
  • EUR 244.00
  • 100ul
  • 50ul
  • Form: Liquid
  • Buffer: -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Antigen affinity purification
Description: A polyclonal antibody against SRC. Recognizes SRC from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IHC;ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:15-1:50

src Antibody

1-CSB-PA24479A0Rb
  • EUR 317.00
  • EUR 335.00
  • 100ul
  • 50ul
  • Form: Liquid
  • Buffer: Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 >95%, Protein G purified
Description: A polyclonal antibody against src. Recognizes src from Zebrafish. This antibody is Unconjugated. Tested in the following application: ELISA, WB; Recommended dilution: WB:1:500-1:5000

Src antibody

70R-37554 100 ug
EUR 273
Description: Rabbit Polyclonal Src antibody

Src antibody

70R-37603 100 ug
EUR 273
Description: Rabbit Polyclonal Src antibody

Src antibody

70R-32504 100 ug
EUR 327
Description: Rabbit polyclonal Src antibody

Src antibody

70R-32507 100 ug
EUR 327
Description: Rabbit polyclonal Src antibody

Src antibody

70R-32737 100 ug
EUR 327
Description: Rabbit polyclonal Src antibody

Src antibody

70R-34409 100 ug
EUR 327
Description: Rabbit polyclonal Src antibody
hicstatistics
Melting dsDNA Donor Molecules Vastly Improves Precision Genome Enhancing in Caenorhabditiselegans

CRISPR genome modifying has revolutionized genetics in quite a few organisms. Contained in the nematode Caenorhabditiselegans one injection into every of the 2 gonad arms of an grownup hermaphrodite exposes tons of of meiotic germ cells to modifying mixtures, allowing the restoration of a variety of indels or small precision edits from every successfully injected animal. Sadly, significantly for extended insertions, modifying efficiencies can differ broadly, necessitating a variety of injections, and customarily requiring co-selection methods.

 

Correct proper right here we present that melting double stranded DNA (dsDNA) donor molecules earlier to injection will enhance the frequency of tangible homology-directed restore (HDR) by a variety of fold for longer edits. We describe troubleshooting methods that let persistently excessive modifying efficiencies ensuing, as an illustration, in as rather a lot as 100 unbiased GFP knock-ins from a single injected animal. These efficiencies make C. elegans by far the perfect metazoan to genome edit, eradicating limitations to the use and adoption of this facile system as a mannequin for understanding animal biology.

 

Water-Pipe Smoking Publicity Deregulates a Set of Genes Related to Human Head and Neck Most cancers Improvement and Prognosis

  • Water-pipe smoking (WPS) is popping into in all probability probably the most well-liked kind of tobacco use among the many many many youth, notably contained in the Coronary heart East, altering cigarettes quickly and turning into a crucial danger of tobacco dependancy worldwide. Smoke from WPS accommodates comparable toxins as these current in cigarette smoke and is linked instantly with plenty of sorts of cancers together with lung and head and neck (HN) carcinomas.

 

  • Nonetheless, the underlying molecular pathways and/or goal genes accountable for the carcinogenic course of are nonetheless unknown. On this research, human widespread oral epithelial (HNOE) cells, NanoStringPanCancer Pathways panel of 770 gene transcripts and quantitative real-time polymerase chain response (qRT-PCR) evaluation had been utilized to hunt out differentially expressed genes (DEG) modulated by WPS. In silico evaluation was carried out to analysis the have an effect on of those genes in HN most cancers affected specific particular person’s biology and consequence. We discovered that WPS can induce the epithelial-mesenchymal transition (EMT: hallmark of most cancers development) of HNOE cells.

 

  • Additional considerably, our evaluation of NanoString revealed 23 genes deregulated beneath the have an effect on of WPS, accountable for the modulation of cell cycle, proliferation, migration/invasion, apoptosis, sign transduction, and inflammatory response. Further evaluation was carried out utilizing qRT-PCR of HNOE WPS-exposed and unexposed cells supported the reliability of our NanoString data.

 

  • Furthermore, we exhibit these DEG to be upregulated in most cancers in distinction with widespread tissue. Utilizing the Kaplan-Meier evaluation, we seen a major affiliation between WPS-deregulated genes and relapse-free survival/full survival in HN most cancers victims. Our findings level out that WPS can modulate EMT together with a set of genes which may very well be instantly concerned in human HN carcinogenesis, thereby affecting HN most cancers victims’ survival.
hicstatistics
hicstatistics

A pilot research on the genetic differ of Mycobacterium tuberculosis troublesome strains from tuberculosis victims contained in the Littoral area of Cameroon

Background: The re-emergence of tuberculosis (TB) worldwide, compounded by multi-drug resistance (MDR) of the causative brokers constitutes a major concern to the administration of the illness. Speedy analysis and correct stress identification are pivotal to the administration of the illness. This pilot research investigated the genetic differ of Mycobacterium tuberculosis troublesome (MTBC) strains from TB victims contained in the Littoral area of Cameroon together with their resistance to rifampicin (RIF).

 

Victims and strategies: This was a cross sectional hospital-based research carried out between January and December 2017 and together with 158 isolates from sputum smear constructive people [105 (66.5%) males and 53 (33.5%) females]. Sputum samples had been examined utilizing Xpert MTB/RIF, adopted by customized on Lowenstein-Jensen medium. Isolates had been additional subjected to molecular characterization utilizing IS6110 typing, deletion evaluation and spoligotyping.

 

Outcomes: 13 (8.8%) of the 147 isolates with susceptibility outcomes accessible had been proof in direction of RIF. Drug resistance occurred in 5/50 (10%) feminine in contrast with 8/97 (8.2%) male (OR, 0.81; 0.25-2.62; p = 0.764), and there was no essential distinction all by means of the age ranges (p = 0.448). Nonetheless, RIF resistance was related (OR, 0.18, 95%CI, 0.05-0.69; p = 0.023) with beforehand handled victims [(4/14 (28.6%)] in contrast with new ones [9/133 (6.8%)].

The 150 acknowledged lineages included amongst others 54 (36%) Cameroon, 18 (12%) UgandaI, 32 (21.3%) Haarlem, 17 (11.3%) Ghana, 9(6%) West African 1, 7(4.7%) Delhi/CAS, 4 (2.7%) LAM and three (2%) UgandaII. Of the 150 isolates, a really highly effective cluster was the Cameroon SIT 61, with 43(28.7%) isolates. Six (35.3%) of the 17 UgandaI sub-lineage had been RIF resistant (OR, 9.58; 95%CI, 2.74-33.55, p = 0.001).

 

Conclusion: The cosmopolitan Littoral area presents with a giant Mycobacterium tuberculosis (MTB) strains differ and the UgandaI sub-lineage attainable related to RIF resistance. Understanding the unfold of this clade by the use of surveillance will improve TB administration contained in the area.

 

Human Pim-1 Oncogene (PIM1) ELISA Kit
DLR-PIM1-Hu-96T 96T
EUR 673
  • Should the Human Pim-1 Oncogene (PIM1) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Human Pim-1 Oncogene (PIM1) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Rat Pim-1 Oncogene (PIM1) ELISA Kit
DLR-PIM1-Ra-48T 48T
EUR 549
  • Should the Rat Pim-1 Oncogene (PIM1) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Pim-1 Oncogene (PIM1) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Rat Pim-1 Oncogene (PIM1) ELISA Kit
DLR-PIM1-Ra-96T 96T
EUR 718
  • Should the Rat Pim-1 Oncogene (PIM1) ELISA Kit is proven to show malperformance, you will receive a refund or a free replacement.
Description: A sandwich quantitative ELISA assay kit for detection of Rat Pim-1 Oncogene (PIM1) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
Human Pim-1 Oncogene (PIM1) ELISA Kit
RDR-PIM1-Hu-48Tests 48 Tests
EUR 544
Human Pim-1 Oncogene (PIM1) ELISA Kit
RDR-PIM1-Hu-96Tests 96 Tests
EUR 756
Rat Pim-1 Oncogene (PIM1) ELISA Kit
RDR-PIM1-Ra-48Tests 48 Tests
EUR 583
Rat Pim-1 Oncogene (PIM1) ELISA Kit
RDR-PIM1-Ra-96Tests 96 Tests
EUR 811
Human Pim-1 Oncogene (PIM1) ELISA Kit
RD-PIM1-Hu-48Tests 48 Tests
EUR 521
Human Pim-1 Oncogene (PIM1) ELISA Kit
RD-PIM1-Hu-96Tests 96 Tests
EUR 723
Rat Pim-1 Oncogene (PIM1) ELISA Kit
RD-PIM1-Ra-48Tests 48 Tests
EUR 557
Rat Pim-1 Oncogene (PIM1) ELISA Kit
RD-PIM1-Ra-96Tests 96 Tests
EUR 775
Pim-1 Oncogene (PIM1) Antibody
20-abx101233
  • EUR 425.00
  • EUR 133.00
  • EUR 1205.00
  • EUR 578.00
  • EUR 328.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.
Pim-1 Oncogene (PIM1) Antibody
20-abx101234
  • EUR 439.00
  • EUR 133.00
  • EUR 1233.00
  • EUR 592.00
  • EUR 328.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.
Pim-1 Oncogene (PIM1) Antibody
20-abx101235
  • EUR 453.00
  • EUR 133.00
  • EUR 1302.00
  • EUR 620.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-12 working days.
Pim-1 Oncogene (PIM1) Antibody
abx146417-100ug 100 ug
EUR 391
  • Shipped within 5-10 working days.
Pim-1 Oncogene (PIM1) Antibody
20-abx174066
  • EUR 857.00
  • EUR 439.00
  • 1 mg
  • 200 ug
  • Please enquire.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse)
4-PAC578Mu01
  • EUR 251.00
  • EUR 2576.00
  • EUR 640.00
  • EUR 316.00
  • EUR 215.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1)
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat)
4-PAC578Ra01
  • EUR 259.00
  • EUR 2708.00
  • EUR 670.00
  • EUR 328.00
  • EUR 219.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1)
Recombinant Pim-1 Oncogene (PIM1)
4-RPC578Hu01
  • EUR 467.36
  • EUR 228.00
  • EUR 1477.60
  • EUR 559.20
  • EUR 1018.40
  • EUR 376.00
  • EUR 3544.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
  • Uniprot ID: P11309
  • Buffer composition: PBS, pH 7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
  • Form: Freeze-dried powder
  • Predicted Molecular Mass (KD): 47.8kDa
  • Isoelectric Point: 5.8
Description: Recombinant Human Pim-1 Oncogene expressed in: E.coli
Recombinant Pim-1 Oncogene (PIM1)
4-RPC578Mu01
  • EUR 476.32
  • EUR 230.00
  • EUR 1511.20
  • EUR 570.40
  • EUR 1040.80
  • EUR 382.00
  • EUR 3628.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
  • Uniprot ID: P06803
  • Buffer composition: 20mM Tris, 150mM NaCl, pH8.0, containing 1mM EDTA, 1mM DTT, 0.01% SKL, 5% Trehalose and Proclin300.
  • Form: Freeze-dried powder
  • Predicted Molecular Mass (KD): 17.1kDa
  • Isoelectric Point: 5.6
Description: Recombinant Mouse Pim-1 Oncogene expressed in: E.coli
Recombinant Pim-1 Oncogene (PIM1)
4-RPC578Ra01
  • EUR 467.36
  • EUR 228.00
  • EUR 1477.60
  • EUR 559.20
  • EUR 1018.40
  • EUR 376.00
  • EUR 3544.00
  • 100 ug
  • 10ug
  • 1 mg
  • 200 ug
  • 500 ug
  • 50ug
  • 5 mg
  • Uniprot ID: P26794
  • Buffer composition: PBS, pH 7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
  • Form: Freeze-dried powder
  • Predicted Molecular Mass (KD): 17.4kDa
  • Isoelectric Point: Inquire
Description: Recombinant Rat Pim-1 Oncogene expressed in: E.coli
Pim-1 Oncogene (PIM1) Antibody (Biotin)
20-abx271779
  • EUR 453.00
  • EUR 244.00
  • EUR 1316.00
  • EUR 620.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-15 working days.
Pim-1 Oncogene (PIM1) Antibody (Biotin)
20-abx272590
  • EUR 467.00
  • EUR 244.00
  • EUR 1344.00
  • EUR 634.00
  • EUR 342.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-15 working days.
Pim-1 Oncogene (PIM1) Antibody (Biotin)
20-abx273089
  • EUR 481.00
  • EUR 244.00
  • EUR 1414.00
  • EUR 662.00
  • EUR 356.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-15 working days.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), APC
4-PAC578Mu01-APC
  • EUR 351.00
  • EUR 3365.00
  • EUR 935.00
  • EUR 449.00
  • EUR 222.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with APC.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), Biotinylated
4-PAC578Mu01-Biotin
  • EUR 316.00
  • EUR 2526.00
  • EUR 744.00
  • EUR 387.00
  • EUR 221.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with Biotin.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), Cy3
4-PAC578Mu01-Cy3
  • EUR 427.00
  • EUR 4445.00
  • EUR 1205.00
  • EUR 557.00
  • EUR 254.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with Cy3.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), FITC
4-PAC578Mu01-FITC
  • EUR 301.00
  • EUR 2712.00
  • EUR 768.00
  • EUR 379.00
  • EUR 197.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with FITC.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), HRP
4-PAC578Mu01-HRP
  • EUR 321.00
  • EUR 2933.00
  • EUR 827.00
  • EUR 405.00
  • EUR 209.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with HRP.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), PE
4-PAC578Mu01-PE
  • EUR 301.00
  • EUR 2712.00
  • EUR 768.00
  • EUR 379.00
  • EUR 197.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with PE.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), APC
4-PAC578Ra01-APC
  • EUR 364.00
  • EUR 3545.00
  • EUR 980.00
  • EUR 467.00
  • EUR 227.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with APC.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), Biotinylated
4-PAC578Ra01-Biotin
  • EUR 325.00
  • EUR 2658.00
  • EUR 777.00
  • EUR 400.00
  • EUR 225.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with Biotin.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), Cy3
4-PAC578Ra01-Cy3
  • EUR 444.00
  • EUR 4685.00
  • EUR 1265.00
  • EUR 581.00
  • EUR 261.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with Cy3.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), FITC
4-PAC578Ra01-FITC
  • EUR 311.00
  • EUR 2856.00
  • EUR 804.00
  • EUR 393.00
  • EUR 202.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with FITC.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), HRP
4-PAC578Ra01-HRP
  • EUR 332.00
  • EUR 3089.00
  • EUR 866.00
  • EUR 421.00
  • EUR 213.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with HRP.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), PE
4-PAC578Ra01-PE
  • EUR 311.00
  • EUR 2856.00
  • EUR 804.00
  • EUR 393.00
  • EUR 202.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with PE.
Human Pim-1 Oncogene (PIM1) Protein
20-abx068546
  • EUR 648.00
  • EUR 272.00
  • EUR 1998.00
  • EUR 773.00
  • EUR 467.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-12 working days.
Rat Pim-1 Oncogene (PIM1) Protein
20-abx068547
  • EUR 648.00
  • EUR 272.00
  • EUR 1998.00
  • EUR 773.00
  • EUR 467.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-15 working days.
Mouse Pim-1 Oncogene (PIM1) Protein
20-abx068548
  • EUR 662.00
  • EUR 272.00
  • EUR 2040.00
  • EUR 787.00
  • EUR 481.00
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug
  • Shipped within 5-7 working days.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Human, Mouse, Rat)
4-PAC578Hu01
  • EUR 247.00
  • EUR 2510.00
  • EUR 625.00
  • EUR 310.00
  • EUR 214.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr129~Leu268)
  • Buffer composition: 0.01M PBS, pH7.4, containing 0.05% Proclin-300, 50% glycerol.
Description: A Rabbit polyclonal antibody against Human, Mouse, Rat Pim-1 Oncogene (PIM1)
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Mouse), APC-Cy7
4-PAC578Mu01-APC-Cy7
  • EUR 583.00
  • EUR 6610.00
  • EUR 1750.00
  • EUR 778.00
  • EUR 324.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr122~Leu261)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Mouse Pim-1 Oncogene (PIM1). This antibody is labeled with APC-Cy7.
Pim-1 Oncogene (PIM1) Polyclonal Antibody (Rat), APC-Cy7
4-PAC578Ra01-APC-Cy7
  • EUR 608.00
  • EUR 6970.00
  • EUR 1840.00
  • EUR 814.00
  • EUR 335.00
  • 100ul
  • 10ml
  • 1ml
  • 200ul
  • 20ul
  • Sequence of the immunogen: PIM1 (Tyr38~Leu177)
  • Buffer composition: PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
Description: A Rabbit polyclonal antibody against Rat Pim-1 Oncogene (PIM1). This antibody is labeled with APC-Cy7.
Human Pim-1 Oncogene (PIM1)ELISA Kit
201-12-2345 96 tests
EUR 440
  • This Pim-1 Oncogene ELISA kit is validated to work with samples from whole blood, serum, plasma and cell culture supernatant.
Description: A quantitative ELISA kit for measuring Human in samples from biological fluids.
Human Pim-1 Oncogene (PIM1) CLIA Kit
20-abx190030
  • EUR 7911.00
  • EUR 4215.00
  • EUR 973.00
  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests
  • Shipped within 5-7 working days.
Human Pim-1 Oncogene (PIM1) ELISA Kit
20-abx152744
  • EUR 7378.00
  • EUR 3933.00
  • EUR 911.00
  • 10 × 96 tests
  • 5 × 96 tests
  • 96 tests
  • Shipped within 5-7 working days.
Human Pim-1 Oncogene (PIM1) ELISA Kit
abx573560-96tests 96 tests
EUR 668
  • Shipped within 5-12 working days.
Cow Pim-1 Oncogene (PIM1) ELISA Kit
abx519080-96tests 96 tests
EUR 911
  • Shipped within 5-12 working days.
Mouse Pim-1 Oncogene (PIM1) ELISA Kit
abx519082-96tests 96 tests
EUR 668
  • Shipped within 5-12 working days.
Rat Pim-1 Oncogene (PIM1) ELISA Kit
abx519083-96tests 96 tests
EUR 668
  • Shipped within 5-12 working days.
Human Pim-1 Oncogene(PIM1)ELISA Kit
QY-E04698 96T
EUR 361
Rat Pim-1 Oncogene(PIM1)ELISA Kit
QY-E10539 96T
EUR 400
Human Pim-1 Oncogene ELISA Kit (PIM1)
RK02083 96 Tests
EUR 521
Human Pim-1 Oncogene (PIM1)CLIA Kit
SCC578Hu-10x96wellstestplate 10x96-wells test plate
EUR 5647.8
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-1 Oncogene (PIM1) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-1 Oncogene (PIM1) in serum, plasma, tissue homogenates, cell culture supernates and other biological fluids.
Human Pim-1 Oncogene (PIM1)CLIA Kit
SCC578Hu-1x48wellstestplate 1x48-wells test plate
EUR 552.76
  • The Intra-assay Precision is determined when 3 samples with low, middle and high level of Human Pim-1 Oncogene (PIM1) were tested on 3 different plates, 8 replicates in each plate
  • CV(%) = SD/meanX100
  • Intra-Assay: CV<10%
  • Inter-Assay: CV<12%
Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Human Pim-1 Oncogene (PIM1) in serum, plasma, tissue homogenates, cell culture supernates and other biological fluids.
Human Pim-1 Oncogene (PIM1)CLIA Kit
SCC578Hu-1x96wellstestplate 1x96-wells test plate