ANT4 Polyclonal Antibody, 100ul Cell Culture Plates Mutations in this gene are

Mutations in this gene are associated with ectodermal dysplasia| and cleft lip/palate syndrome 3 (EEC3)

but also serve as scaffolding platforms for the assembly

Multiple transcript variants encoding different isoforms have been found for COQ8B

Mouse studies also indicated that the Ras-GEF signaling pathway mediated by this protein may be important for long-term memory

Component of the cytosolic iron-sulfur protein assembly (CIA) complex

ANT4 Polyclonal Antibody, 100ul Cell Culture Plates Mutations in this gene areSolute carrier family 25 member 31 encoded by SLC25A31 is a member of the ADP ATP carrier family of proteins that exchange cytosolic ADP for matrix ATP in the mitochondria. Cells over expressing this gene have been shown to display an anti apoptotic phenotype. This protein is also thought to play a role in spermatogenesis, where it is believed to associate with a part of the flagellar cytoskeleton and with glycolytic enzymes. Male mice with mutations