VHL Polyclonal Antibody, 50ul[BT-AP15472] Antibody Humanization Variation at this gene has

Variation at this gene has been observed in patients with absorptive hypercalciuria

Additional transcript variants of this gene have been described| but their full-length nature is not known

Induces cell shedding simply by lowering the temperature - straightforward

It contains a Sec7 domain

and there are putative pseudogenes on other chromosomes

VHL Polyclonal Antibody, 50ul[BT-AP15472] Antibody Humanization Variation at this gene hasVon 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. This protein is involved in the ubiquitination and