NBPF4 Polyclonal Antibody, 50ul Isothermal Amplification Encoded by a gene that

Encoded by a gene that maps to human chromosome 7q34

This gene rearranges with the trk proto-oncogene t

such as ZNF272

in intralumenal endosomal vesicle formation

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

NBPF4 Polyclonal Antibody, 50ul Isothermal Amplification Encoded by a gene thatNBPF4 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