ATS15 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification and amidation

and amidation

CCL4 is secreted from activated monocytes as a heterodimer with CCL3/MIP-1 alpha

Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease

Rotor capacity:2mL/1

Defects in C1S are the cause of selective C1s deficiency

ATS15 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification and amidationThis gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C terminal TS motifs, and some have unique C terminal domains. The encoded