S2546 Rabbit Polyclonal Antibody, 100ul Serum each encoding a distinct carboxyl

each encoding a distinct carboxyl terminus

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

Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis

which was reported to interact with 26S proteasome

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

S2546 Rabbit Polyclonal Antibody, 100ul Serum each encoding a distinct carboxylThis 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.