S2546 Rabbit Polyclonal Antibody, 100ul Serum have been described for BRCA1

have been described for BRCA1

Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

20-lyase activities and is a key enzyme in the steroidogenic pathway that produces progestins

Expression of this protein is increased after the activation of T-cells by mitogens or the activation of NK cells by IL-2

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

S2546 Rabbit Polyclonal Antibody, 100ul Serum have been described for BRCA1This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy.