Bovine Metalloproteinase Inhibitor 2, TIMP2 ELISA Kit , 96T Serum This gene encodes a member

This gene encodes a member of a family of proteins containing several distinct regions

essential for T-cell proliferation and IFNG production in a PDCD1-independent manner

Defects in CLDN19 are the cause of hypomagnesemia renal with ocular involvement (HOMGO)

Defects in this gene are cause of an autosomal recessive cutis laxa syndrome

It is related to epidermal growth factor (EGF) and transforming growth factor alpha (TGF-alpha)

Bovine Metalloproteinase Inhibitor 2, TIMP2 ELISA Kit , 96T Serum This gene encodes a memberComplexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor.