Bio-Connect
WB analysis of 293, HepG2, Jurkat, and COLO cell lysates using GTX87305 NBPF1/9/10/12/14/15/16/20 antibody. The lane on the right is blocked with the synthesized peptide.
WB analysis of 293, HepG2, Jurkat, and COLO cell lysates using GTX87305 NBPF1/9/10/12/14/15/16/20 antibody. The lane on the right is blocked with the synthesized peptide.
WB analysis of 293, HepG2, Jurkat, and COLO cell lysates using GTX87305 NBPF1/9/10/12/14/15/16/20 antibody. The lane on the right is blocked with the synthesized peptide.

NBPF1/9/10/12/14/15/16/20 antibody

GTX87305
GeneTex
TargetNBPF1
Product group Antibodies
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    NBPF1/9/10/12/14/15/16/20 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500~1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Formulation
    Liquid
  • Gene ID55672
  • Target name
    NBPF1
  • Target description
    NBPF member 1
  • Target synonyms
    AB13; AB14; AB23; AD2; NBG; NBPF; neuroblastoma breakpoint family member 1
  • Protein IDQ3BBV0
  • Protein Name
    Neuroblastoma breakpoint family member 1
  • Scientific Description
    This gene 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 variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, mental retardation, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Apr 2013]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203