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VHL Rabbit anti-Human, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 247561AP150UL
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
| 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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