C1QA Polyclonal Antibody, 100ul Nucleic Acid Amplification activation of a MAP kinase

activation of a MAP kinase signaling pathway

It may also be required for the assembly of membrane and secretory proteins

This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

and a pseudogene of this gene is located on the long arm of chromosome 5

the centripetal movement of lysosomes and endosomes

C1QA Polyclonal Antibody, 100ul Nucleic Acid Amplification activation of a MAP kinaseThis gene encodes a major constituent of the human complement subcomponent C1q. C1q associates with C1r and C1s in order to yield the first component of the serum complement system. Deficiency of C1q has been associated with lupus erythematosus and glomerulonephritis. C1q is composed of 18 polypeptide chains: six A chains, six B chains, and six C chains. Each chain contains a collagen like region located near the N terminus and a C terminal globular