CLC14 Polyclonal Antibody, 20ul Multiplex Immunoassays it localizes in the caudal

it localizes in the caudal region of the head to the end of the principal piece

and inhibition of apoptosis

Mutations in this gene cause speech-language disorder 1 (SPCH1)

This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family

skin and musculoskeletal abnormalities

CLC14 Polyclonal Antibody, 20ul Multiplex Immunoassays it localizes in the caudalThis gene encodes a member of the C type lectin C type lectin like domain (CTL CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This family member plays a role in cell cell adhesion and angiogenesis. It functions in filopodia formation, cell migration and tube formation. Due to its presence