P Polyclonal Antibody, 20ul Sample Library Tubes This protein plays a key

This protein plays a key role in cell surface structure adhesion

Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia

memory B cell development

possibly by cyclinB/cdc2

A chromosomal translocation t(10

P Polyclonal Antibody, 20ul Sample Library Tubes This protein plays a keyThis gene encodes the human homolog of the mouse p (pink eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism.