TRPC3 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in this gene have

Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome

RCVRN (recoverin) encodes a member of the recoverin family of neuronal calcium sensors

IQCB1 encodes a nephrocystin protein that interacts with calmodulin and the retinitis pigmentosa GTPase regulator protein

MITF encodes microphthalmia-associated transcription factor that contains both basic helix-loop-helix and leucine zipper structural features

This member is a cytosolic protein

TRPC3 Polyclonal Antibody, 100ul Cellular Function Assays Mutations in this gene haveShort transient receptor potential channel 3 encoded by TRPC3 is a membrane protein that can form a non selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene.