GTF2IRD2B anticorps (C-Term)

N° du produit ABIN1881397

Détail du produit anti-GTF2IRD2B anticorps

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

Épitope: AA 467-494, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GTF2IRD2B est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: 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.

Clone: RB40709

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Date de péremption: 6 months

Références pour anticorps anti-GTF2IRD2B (ABIN1881397)

Hinsley, Cunliffe, Tipney, Brass, Tassabehji: "Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome." dans: 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." dans: European journal of human genetics : EJHG, Vol. 12, Issue 7, pp. 551-60, (2004) (PubMed).

Détails sur GTF2IRD2B

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

Autre désignation: GTF2IRD2B (GTF2IRD2B Produits)

Sujet: 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.

Poids moléculaire: 107233

NCBI Accession: NP_001003795

UniProt: Q6EKJ0