NBPF6 antibody (C-Term)

Catalog No. ABIN2791688

This Rabbit Polyclonal antibody specifically detects NBPF6 in WB. It exhibits reactivity toward Human and Rat.

Quick Overview for NBPF6 antibody (C-Term) (ABIN2791688)

Target: NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NBPF6 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-NBPF6 Antibody

Binding Specificity: C-Term

Sequence: STLYSFEDKQ VSLALVDKIK KDQEEIEDQS PPCPRLSQEL PEVKEQEVPE

Predicted Reactivity: Human: 100%, Rat: 75%

Characteristics: This is a rabbit polyclonal antibody against NBPF6. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the C-terminal region of Human NBPF6

Application Details

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

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

Handling Advice: Avoid repeat freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for NBPF6

Target: NBPF6 (Neuroblastoma Breakpoint Family, Member 6 (NBPF6))

Alternative Name: NBPF6

Background: 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.
Alias Symbols: -
Protein Size: 667

Molecular Weight: 75 kDa

Gene ID: 653149

NCBI Accession: NM_001143987, NP_001137459

UniProt: E9PDL3