IKK gamma(Phospho Ser376) Polyclonal Antibody, 50ul Subcellular Fractions Mutations in this gene are

Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome

transducin beta like 2 is possibly involved in some intracellular signaling pathway

the latter a human homolog of the Drosophilia jagged receptor notch

vent cap feature

This gene encodes a protein which shares sequence similarity with other members of the type II chaperonin family

IKK gamma(Phospho Ser376) Polyclonal Antibody, 50ul Subcellular Fractions Mutations in this gene areThis gene encodes the regulatory subunit of the inhibitor of kappaB kinase (IKK) complex which activates NF kappaB resulting in activation of genes involved in inflammation immunity cell survival and other pathways. Mutations in this gene result in incontinentia pigmenti hypohidrotic ectodermal dysplasia and several other types of immunodeficiencies. A pseudogene highly similar to this locus is located in an adjacent region of the X chromosome.