NBPF4 Polyclonal Antibody, 50ul Isothermal Amplification such as ZNF272

such as ZNF272

Defects in this gene are cause of an autosomal recessive cutis laxa syndrome

An important paralog of this gene is PATZ1

Peroxisomal biogenesis factor 14 is integrated into peroxisome membranes with its C-terminus exposed to the cytosol

also confers a high incidence of breast cancer

NBPF4 Polyclonal Antibody, 50ul Isothermal Amplification such as ZNF272NBPF4 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. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number