VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma including platelet dense granules and

including platelet dense granules and melanosomes

PTM:Phosphorylated on tyrosines by FYN (By similarity)

and returns it to the ER

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

14-cis-eicosatetrenoic acid (leukotriene A4)

VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma including platelet dense granules andVon 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