CD58 Polyclonal Antibody, 100ul[BT-AP01842] Filtration The proteins encoded by the

The proteins encoded by the gene family are inhibitors of the matrix metalloproteinases

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene

RAB GTPase Binding Effector Protein 1) is a Protein Coding gene

allowing for a wide range of liquid transfer needs

2001 [PubMed 12063393])

CD58 Polyclonal Antibody, 100ul[BT-AP01842] Filtration The proteins encoded by theThe product of CLDN19 belongs to the claudin family. It plays a major role in tight junction specific obliteration of the intercellular space, through calcium independent cell adhesion activity. Defects in CLDN19 are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe