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VHL Polyclonal Antibody, 100μg, (ATB-T4876)

$199.00
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Product Details

Background: Von Hippel-Lindau syndrome (VHL) is a dominantly inherited familial cancer syndrome predisposing to a variety of malignant and benign tumors. A germline mutation of this gene is the basis of familial inheritance of VHL syndrome. The protein encoded by this gene is a component of the protein complex that includes elongin B, elongin C, and cullin-2, and possesses ubiquitin ligase E3 activity. This protein is involved in the ubiquitination and degradation of hypoxia-inducible-factor (HIF), which is a transcription factor that plays a central role in the regulation of gene expression by oxygen. RNA polymerase II subunit POLR2G/RPB7 is also reported to be a target of this protein. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]Product datasheet: Overview Product Description VHL Polyclonal Antibody, 100μg, (ATB-T4876) Species Reactivities Human,Mouse,Rat Immunogen Synthesized peptide derived from human VHL around the non-phosphorylation site of S68. Properties Form Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. Storage Instructions-20°C/1 year References: Mutational status of VHL gene and its clinical importance in renal clear cell carcinoma. Alves MR, et al. Virchows Arch, 2014 Sep. PMID 25027579 von Hippel-Lindau exonic methylation analysis using MALDI-TOF mass spectrometry. Lian F, et al. J Urol, 2014 Nov. PMID 24704013 De novo VHL germline mutation detected in a patient with mild clinical phenotype of von Hippel-Lindau disease. Ding X, et al. J Neurosurg, 2014 Aug. PMID 24678776 The multifaceted von Hippel-Lindau tumour suppressor protein. Robinson CM, et al. FEBS Lett, 2014 Aug 19. PMID 24583008 Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients. Wang X, et al. Urology, 2014 Mar. PMID 24581539

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VHL Polyclonal Antibody, 100μg, (ATB-T4876)
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