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Background: |
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. |
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Applications: |
ELISA, WB, IHC |
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Name of antibody: |
VHL |
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Immunogen: |
Full length fusion protein |
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Full name: |
von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase |
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Synonyms： |
RCA1; VHL1; pVHL; HRCA1 |
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SwissProt: |
P40337 |
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ELISA Recommended dilution: |
2000-5000 |
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IHC positive control: |
Human colon cancer and Human thyroid cancer |
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IHC Recommend dilution: |
25-100 |
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WB Predicted band size: |
24 kDa |
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WB Positive control: |
Human fetal brain tissue |
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WB Recommended dilution: |
500-2000 |
