NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody, 100ul ROS/Nitric Oxide Detection a process which occurs normally

a process which occurs normally during development but also during metastasis

reducing fatigue and offering a smoother

Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

This gene contains a variable number of tandem repeat (VNTR) polymorphism in the coding region that may influence the function of the encoded protein

NBPF1/9/10/12/14/15/16/20 Polyclonal Antibody, 100ul ROS/Nitric Oxide Detection a process which occurs normallyNBPF1 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