ATP7B Polyclonal Antibody, 100ul Cryopreservation where the phosphorylated form is

where the phosphorylated form is bound to a 14-3-3 protein

and pleckstrin homology (PH) domains

Mutations in this gene may be associated with adult-onset sensorimotor neuropathy

NBPF1 is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1

ATP7B Polyclonal Antibody, 100ul Cryopreservation where the phosphorylated form isATP7B (ATPase copper transporting beta) is a member of the P type cation transport ATPase family and encodes a protein with several membrane spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding