P Polyclonal Antibody, 20ul Sample Library Tubes A chromosomal translocation t(10

A chromosomal translocation t(10

is involved in the regulation of various phosphoinositides

Mutations in this gene cause steroid-resistant nephrotic syndrome

The antibody can recognize isoform1 and isoform2 of CDH24

and plays a role in regulating the migration of tumor cells

P Polyclonal Antibody, 20ul Sample Library Tubes A chromosomal translocation t(10This 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.