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VHL Mouse anti-Human, Clone: OTI1E1, liquid, TrueMAB™
SDP

Catalog No. 501676540
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100 μL
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50-167-6540 100 μL
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Catalog No. 50-167-6540 Supplier OriGene Supplier No. TA506222
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Mouse Monoclonal Antibody

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

Antigen VHL
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Monoclonal
Clone OTI1E1
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.02% sodium azide
Gene VHL
Gene Accession No. P40337
Gene Alias HRCA1, RCA1, VHL1, pVHL
Gene Symbols VHL
Host Species Mouse
Immunogen Full length human recombit protein of human VHL produced in HEK293T cell.
Purification Method Affinity Chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 7428
Target Species Human
Content And Storage -20° C, Avoid Freeze/Thaw Cycles
Product Type Antibody
Form Liquid
Isotype IgG2b
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