NBPF7 antibody (AA 361-410)

Catalog No. ABIN1535096

The Rabbit Polyclonal anti-NBPF7 antibody (ABIN1535096) specifically detects NBPF7 in WB and IHC. The antibody is reactive with Human, Mouse and Rat samples.

Quick Overview for NBPF7 antibody (AA 361-410) (ABIN1535096)

Target: NBPF7 (Neuroblastoma Breakpoint Family, Member 7 (NBPF7))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NBPF7 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Product Details anti-NBPF7 Antibody

Binding Specificity: AA 361-410

Purpose: NBPF7 Antibody

Specificity: NBPF7 Polyclonal Antibody detects endogenous levels of NBPF7 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Purity: > 95 %

Immunogen: The antiserum was produced against synthesized peptide derived from human NBPF7. AA range:361-410

Isotype: IgG

Application Details

Application Notes: WB 1:500-2000,IHC 1:50-300

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for NBPF7

Target: NBPF7 (Neuroblastoma Breakpoint Family, Member 7 (NBPF7))

Alternative Name: NBPF7

Background:

Synonyms: NBPF7, Putative neuroblastoma breakpoint family member 7

Background: neuroblastoma breakpoint family member 7(NBPF7) Homo sapiens 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 fam

Gene Name: NBPF7

Protein Name: Putative neuroblastoma breakpoint family member 7

Molecular Weight: 48 kDa

Gene ID: 343505

UniProt: P0C2Y1