GTF2IRD2B antibody (C-Term)

Catalog No. ABIN1881397

This Rabbit Polyclonal antibody specifically detects GTF2IRD2B in WB. It exhibits reactivity toward Human. It has been mentioned in 2+ publications

Quick Overview for GTF2IRD2B antibody (C-Term) (ABIN1881397)

Target: GTF2IRD2B (GTF2I Repeat Domain Containing 2B (GTF2IRD2B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GTF2IRD2B antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB40709

Product Details anti-GTF2IRD2B Antibody

Binding Specificity: AA 467-494, C-Term

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This GTF2IRD2B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 467-494 amino acids from the C-terminal region of human GTF2IRD2B.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Expiry Date: 6 months

References for anti-GTF2IRD2B antibody (ABIN1881397)

Hinsley, Cunliffe, Tipney, Brass, Tassabehji: "Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome." in: Protein science : a publication of the Protein Society, Vol. 13, Issue 10, pp. 2588-99, (2004) (PubMed).

Tipney, Hinsley, Brass, Metcalfe, Donnai, Tassabehji: "Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome." in: European journal of human genetics : EJHG, Vol. 12, Issue 7, pp. 551-60, (2004) (PubMed).

Target Details for GTF2IRD2B

Target: GTF2IRD2B (GTF2I Repeat Domain Containing 2B (GTF2IRD2B))

Alternative Name: GTF2IRD2B

Background: This gene encodes a glycosylated phosphoprotein with a leucine zipper motif, two helix-loop-helix motifs (I repeats) that are similar to domains found in the TFII-I family of transcription factors, one CHARLIE8 transposable element-like sequence, and a BED zinc finger. This gene lies within a region that is deleted in Williams-Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described, however, not all variants have been fully characterized.

Molecular Weight: 107233

NCBI Accession: NP_001003795

UniProt: Q6EKJ0