Nibrin Polyclonal Antibody, 20ul[BT-AP06020] Recombinant Protein Expression A pseudogene of SLC9A7 is

A pseudogene of SLC9A7 is found on chromosome 12

but subsequently was demonstrated to stimulate insulin release in the presence of elevated glucose

such as cell division and regulation of insulin sensitivity

at least one of which encodes a preproprotein that is proteolytically processed to generate two chains that comprise the heterodimeric active enzyme

Nibrin Polyclonal Antibody, 20ul[BT-AP06020] Recombinant Protein Expression A pseudogene of SLC9A7 isMutations in NBN are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. Nibrin is a member of the MRE11 RAD50 double strand break repair complex which consists of 5 proteins. NBN product is thought to be involved in DNA double strand break repair and DNA damage induced checkpoint activation.