CD56 Polyclonal Antibody, 50ul[BT-AP01797] Deep Well Plates an X-linked recessive disorder

an X-linked recessive disorder

playing a role in the morphogenic direction of tissue development

C1R aligns across a gap in the GRCh38 reference genome assembly

This gene is thought to be associated with colon cancer

Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains

CD56 Polyclonal Antibody, 50ul[BT-AP01797] Deep Well Plates an X-linked recessive disorderCMA1 encodes a chymotryptic serine proteinase that belongs to the peptidase family S1. It is expressed in mast cells and is thought to function in the degradation of the extracellular matrix, the regulation of submucosal gland secretion, and the generation of vasoactive peptides. In the heart and blood vessels, this protein, rather than angiotensin converting enzyme, is largely responsible for converting angiotensin I to the vasoactive peptide