NDUFA8 Polyclonal Antibody, 100ul Culture Tubes Mutations of this gene are

Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia

which is also located on chromosome 3

It is also found to support the proliferation of hematopoietic stem cells and megakaryocyte progenitor cells

The subfamily that includes the V2 receptor

NDUFA8 Polyclonal Antibody, 100ul Culture Tubes Mutations of this gene areNADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8 encoded by NDUFA8 belongs to the complex I 19 kDa subunit family. Mammalian complex I is composed of 45 different subunits. This protein has NADH dehydrogenase activity and oxidoreductase activity. It plays an important role in transfering electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing of this