VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma 100mLx12pcs

100mLx12pcs

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

including platelet dense granules and melanosomes

VHL Polyclonal Antibody, 50ul[BT-AP09520] Plasma 100mLx12pcsVon 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