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VHL Rabbit anti-Human, Polyclonal, Proteintech
SDP

Rabbit Polyclonal Antibody

Supplier:  Proteintech Group Inc 247561AP150UL

Encompass_Preferred

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Catalog No. 50-173-4523


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Description

Description

Von Hippel-Lindau syndrome (VHL) is a domitly inherited familial cancer syndrome predisposing to a variety of maligt 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.
Specifications

Specifications

VHL
Polyclonal
Unconjugated
VHL
HRCA1, Protein G7, pVHL, RCA1, VHL, VHL1
Rabbit
Antigen Affinity Chromatography
RUO
7428
-20°C
Liquid
Immunocytochemistry, Immunofluorescence
0.25 mg/mL
PBS with 50% glycerol and 0.1% sodium azide; pH 7.3
P40337
VHL
VHL Fusion Protein Ag21447
150 μL
Primary
Human
Antibody
IgG
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