Cadherin-23 Polyclonal Antibody, 100ul Shakers Defects in this gene are

Defects in this gene are a cause of 3M syndrome type 1 (3M1)

it's also Dnase/Rnase free and non-pyrogenic

Phospholipase C enzymes play a critical role in many cellular processes by hydrolyzing phosphatidylinositol 4|5-bisphosphate into two intracellular second messengers| inositol 1|4|5-trisphosphate and diacylglycerol

sequence Translation N-terminally shortened

spinal cord and adrenal gland

Cadherin-23 Polyclonal Antibody, 100ul Shakers Defects in this gene areCDH23 (cadherin related 23) is a member of the cadherin superfamily, whose genes encode calcium dependent cell cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. CDH23 is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin like gene.