S10A2 Polyclonal Antibody, 50ul Peptide Modification Deficiencies lead to the skeletal

Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia

This gene encodes a member of the 17beta-hydroxysteroid dehydrogenase family of short-chain dehydrogenases/reductases

overspeed detector

The protein is involved in maintaining blood pressure and in the pathogenesis of essential hypertension and preeclampsia

S10A2 Polyclonal Antibody, 50ul Peptide Modification Deficiencies lead to the skeletalThe protein encoded by this gene 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 protein may have a tumor suppressor