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NBPF8 Rabbit anti-Human, Polyclonal, Invitrogen™

Rabbit Polyclonal Antibody

Manufacturer:  Invitrogen PA548240

Catalog No. PA548240


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Description

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]
Specifications

Specifications

NBPF8
Polyclonal
PBS with 0.09% sodium azide
Q3BBV2
Putative neuroblastoma breakpoint family member 8, NBPF8, NBPF8P
Rabbit
IgG
400 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
728841
Immunohistochemistry (Paraffin), Western Blot
Unconjugated
NBPF8
Liquid
NBPF8
KLH conjugated synthetic peptide between 30-58 amino acids from the N-terminal region of human NBPF8.
Antigen Affinity Chromatography, Protein A
RUO
Antibody
Polyclonal
Human
Documents
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