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S-100 Beta Monoclonal Antibody, 100ul Proteases Mutations in CASR cause familial

SKU: 11464454664

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S-100 Beta Monoclonal Antibody, 100ul Proteases Mutations in CASR cause familialThe 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 however, this gene is located at 21q22. 3.

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Description

Mutations in CASR cause familial hypocalciuric hypercalcemia

EIF3C of module C binds EIF3B of module A and EIF3H of module B

The full length form is the transmembrane protein

The MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family consists of six human proteins

53BP1 activates the checkpoint kinase ATM and promotes DNA double strand break repair via nonhomologous end joining (NHEJ) repair pathway

S-100 Beta Monoclonal Antibody, 100ul Proteases Mutations in CASR cause familialThe 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 however, this gene is located at 21q22. 3.

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