F219A Rabbit Polyclonal Antibody, 20ul Pasteur Pipets Retinitis pigmentosa is an inherited

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

The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain

This I-domain containing alpha integrin combines with the beta 2 chain (ITGB2) to form the integrin lymphocyte function-associated antigen-1 (LFA-1)

PAK family members are known to be effectors of Rac/Cdc42 GTPases

and gastric acid

F219A Rabbit Polyclonal Antibody, 20ul Pasteur Pipets Retinitis pigmentosa is an inheritedThe protein encoded by this gene has homologs that have been identified in mouse macaque etc organisms. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.