CdGAP(Phospho Thr789) Polyclonal Antibody, 20ul Cell Screening and Imaging Retinitis pigmentosa is an inherited

Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities

and regulates their signaling activities

where it is involved in transcriptional regulation

This gene product appears to form only homodimers

These studies suggest that this gene product may also be important in T cell function and contribute to the prevention of autoimmune diseases

CdGAP(Phospho Thr789) Polyclonal Antibody, 20ul Cell Screening and Imaging Retinitis pigmentosa is an inheritedThis gene encodes a GTPase activating protein (GAP). A variety of cellular processes are regulated by Rho GTPases which cycle between an inactive form bound to GDP and an active form bound to GTP. This cycling between inactive and active forms is regulated by guanine nucleotide exchange factors and GAPs. The encoded protein is a GAP shown to regulate two GTPases involved in protein trafficking and cell growth.