MMP-7 Polyclonal Antibody, 50ul Reservoirs Activating mutations in this gene

Activating mutations in this gene are a common cause of congenital hyperinsulinism

Involved in embryogenesis and hematopoiesis

whereby deletion of the region encoding this domain results in an oncogene

Interacts with MXI1 to repress MYC responsive genes and antagonize MYC oncogenic activities

MMP-7 Polyclonal Antibody, 50ul Reservoirs Activating mutations in this geneMMP7 encodes a member of the peptidase M10 family of matrix metalloproteinases (MMPs). Proteins in this family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Matrilysin is proteolytically processed to generate the mature protease. This secreted protease breaks down