MMP-8 Polyclonal Antibody, 50ul Primary Antibodies Mutations in this gene are

Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness

tissue specificity:Abundant in adipose tissues

both proteins can inhibit the transcription of cell cycle genes containing E2F binding sites in their promoters

Diseases associated with IFITM2 include west nile virus and stomatitis

which suggested a role in muscle regeneration or differentiation

MMP-8 Polyclonal Antibody, 50ul Primary Antibodies Mutations in this gene areMMP8 encodes a member of the matrix metalloproteinase (MMP) family of proteins. These proteins are involved in the breakdown of extracellular matrix in embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Proteolysis at different sites on this protein results in multiple active forms of the enzyme with distinct N termini. This protein functions in the degradation of type I, II