TIMP-4 Polyclonal Antibody, 50ul[BT-AP09038] Molecular Biology pigmentary retinopathy

pigmentary retinopathy

the human ortholog of Rudhira is 98% identical and the gene maps to a breakpoint of hematological neoplasms on chromosome 17q23

In tissues that do not express the mineralocorticoid receptor

which plays a fundamental role in pathogen recognition and activation of innate immune responses

TIMP-4 Polyclonal Antibody, 50ul[BT-AP09038] Molecular Biology pigmentary retinopathyTIMP4 belongs to the TIMP gene family. Metalloproteinase inhibitor 4 encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. The secreted, netrin domain containing protein encoded by this gene is involved in regulation of platelet aggregation and recruitment and may play role in hormonal regulation and endometrial tissue remodeling.