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Invitrogen™ NBPF7 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5106691

Catalog No. PIPA5106691


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Description

Description

Antibody detects endogenous levels of total NBPF7.

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, Mar 2013].
TRUSTED_SUSTAINABILITY
Specifications

Specifications

NBPF7
Polyclonal
Unconjugated
NBPF7
NBPF7; neuroblastoma breakpoint family member 7; neuroblastoma breakpoint family, member 7; putative neuroblastoma breakpoint family member 7
Rabbit
Affinity chromatography
RUO
343505
-20°C
Liquid
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
P0C2Y1
NBPF7
A synthesized peptide derived from human NBPF7(Accession P0C2Y1), corresponding to amino acid residues E361-N411.
100 μL
Primary
Human, Mouse
Antibody
IgG
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