S-100A3 Polyclonal Antibody, 100ul Gene Editing Allelic variations in this gene

Allelic variations in this gene are associated with heparin cofactor II deficiency

Heterozygous loss-of-function mutations in this gene result in the dominant In(Lu) blood phenotype

It is a single span type I transmembrane protein that contains a 484 aa extracellular region (aa 31‑514) plus a 68 aa C‑terminal cytoplasmic domain

Multiple mutations in this gene have been identified

DNA-binding protein that specifically recognize the sequence 5'-YAAC

S-100A3 Polyclonal Antibody, 100ul Gene Editing Allelic variations in this geneThe protein encoded by S100A3 (S100 calcium binding protein A3) is a member of the S100 family of proteins containing 2 EF hand calcium binding motifs. S100 proteins are localized in the cytoplasm and or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This