VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma but the full-length nature of

but the full-length nature of only three of them have been determined to date

PTM:Phosphorylated on tyrosines by FYN (By similarity)

including platelet dense granules and melanosomes

SIGLECs are typically expressed on cells of the innate immune system

The encoded protein is active in the reversible S-nitrosylation of cysteines in certain proteins

VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma but the full-length nature ofVon 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 is the basis of familial inheritance of VHL syndrome. The protein encoded by VHL 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