SL9C2 Polyclonal Antibody, 100ul Cell Screening and Imaging Defects in this gene are

Defects in this gene are a cause of congenital secretory sodium diarrhea

Two alternatively spliced transcript variants have been found

F11 receptor encoded by this immunoglobulin superfamily gene member is an important regulator of tight junction assembly in epithelia

stimulation of Ca2+ fluxes

SL9C2 Polyclonal Antibody, 100ul Cell Screening and Imaging Defects in this gene areContains an ion transport like region is related to the membrane segments of voltage gated ion channels.,Involved in pH regulation.,Belongs to the monovalent cation: proton antiporter 1 (CPA1) transporter (TC 2. A. 36) family.,Contains 1 cyclic nucleotide binding domain.,