Recombinant Human VHL, His-tagged

Cat.No. : VHL-28605TH
Product Overview : Recombinant full length human Von Hippel Lindau protein with His tag expressed in a baculovirus system; 213 amino acids, 24kDa.
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Description : 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.
Conjugation : HIS
Tissue specificity : Expressed in the adult and fetal brain and kidney.
Form : Liquid
Purity : >90% by SDS-PAGE
Storage buffer : Preservative: NoneConstituents: 20% Glycerol, 20mM Tris Cl, 100mM Potassium chloride, 1mM DTT, 0.2mM EDTA, pH 8.0
Storage : Shipped on dry ice. Upon delivery aliquot and store at -80oC. Avoid freeze / thaw cycles.
Full Length : Full L.
Gene Name VHL von Hippel-Lindau tumor suppressor [ Homo sapiens ]
Official Symbol VHL
Synonyms VHL; von Hippel-Lindau tumor suppressor; von Hippel Lindau syndrome; von Hippel-Lindau disease tumor suppressor; VHL1;
Gene ID 7428
mRNA Refseq NM_000551
Protein Refseq NP_000542
MIM 608537
Uniprot ID P40337
Chromosome Location 3p25.3
Pathway Adaptive Immune System, organism-specific biosystem; Antigen processing: Ubiquitination & Proteasome degradation, organism-specific biosystem; Class I MHC mediated antigen processing & presentation, organism-specific biosystem;
Function protein binding; transcription factor binding;

Not For Human Consumption!

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