MMP21 Rabbit Polyclonal Antibody, 20ul Molecular Biology Mutations in this gene cause

Mutations in this gene cause congenital heart defects

are characterized by an evolutionarily conserved amino acid-sensing motif linked to an intramembranous 7-transmembrane loop region

and a key role in cardiovascular homeostasis

This protein may function as a cell adhesion molecule

The first two N-terminal amino acids can be cleaved from human CCL4 by CD26/DPPIV

MMP21 Rabbit Polyclonal Antibody, 20ul Molecular Biology Mutations in this gene causeThis gene encodes a member of the matrix metalloproteinase family. Proteins in this family are involved in the breakdown of extracellular matrix for both normal physiological processes such as embryonic development reproduction and tissue remodeling and disease processes such as asthma and tumor metastasis. The encoded protein may play an important role in embryogenesis particularly in neuronal cells as well as in lymphocyte development and survival.