NBPF4 antibody (AA 20-100)

Catalog No. ABIN7219800

The Rabbit Polyclonal anti-NBPF4 antibody (ABIN7219800) specifically detects NBPF4 in IHC, ELISA and IF. The antibody is reactive with Human samples.

Quick Overview for NBPF4 antibody (AA 20-100) (ABIN7219800)

Target: NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NBPF4 antibody is un-conjugated

Application: Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Product Details anti-NBPF4 Antibody

Binding Specificity: AA 20-100

Purpose: Rabbit Anti-NBPF4 Polyclonal Antibody

Specificity: NBPF4 Polyclonal Antibody detects endogenous levels of NBPF4 protein.

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

Immunogen: Synthesized peptide derived from the Internal region of human NBPF4 at AA range: 20-100

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for NBPF4

Target: NBPF4 (Neuroblastoma Breakpoint Family, Member 4 (NBPF4))

Alternative Name: NBPF4

Background: NBPF4, Neuroblastoma breakpoint family member 4NBPF4 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. , 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.

Gene ID: 148545

UniProt: Q96M43