Von Hippel-Lindau Disease Tumor Suppressor (VHL) Antibody

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Catalogue No: abx032864
Price: US$326.25
(Size: 50 µl)

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Datasheet SDS
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 VHL gene is the basis of familial inheritance of VHL syndrome. The protein 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.

Target Von Hippel-Lindau Disease Tumor Suppressor (VHL)
Clonality Polyclonal
Reactivity Human, Mouse
Tested Applications ELISA, WB, IHC, IF/ICC, FCM
Host Rabbit
Recommended dilutions WB: 1/2000, IHC-P: 1/25, IF/ICC: 1/25, FCM: 1/25. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 43-71 amino acids from the N-terminal region of human VHL.
Isotype IgG
Form Liquid
Purification Purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC P40337 (UniProt, ExPASy)
UniProt Secondary AC B2RE45, Q13599, Q6PDA9
UniProt Entry Name VHL_HUMAN
NCBI Accession NP_000542.1 NP_937799.1
KEGG hsa:7428
String 9606.ENSP00000256474
Molecular Weight Calculated MW: 24.2 kDa
Buffer PBS containing 0.09% sodium azide.
Specificity Predicted to react with Rat VHL.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Von Hippel-Lindau Disease Tumor Suppressor (VHL)


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