GTF2I anticorps

N° du produit ABIN7263933

Détail du produit anti-GTF2I anticorps

Antigène: GTF2I (General Transcription Factor III (GTF2I))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GTF2I est non-conjugé

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

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: A synthetic peptide of human GTF2I

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IHC 1:100-1:200 IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur GTF2I

Antigène: GTF2I (General Transcription Factor III (GTF2I))

Autre désignation: GTF2I (GTF2I Produits)

Synonymes: anticorps BAP135, anticorps BTKAP1, anticorps DIWS, anticorps GTFII-I, anticorps IB291, anticorps SPIN, anticorps TFII-I, anticorps WBS, anticorps WBSCR6, anticorps Gtf2ird1, anticorps 6030441I21Rik, anticorps BAP-135, anticorps GtfII-I, anticorps Spin, anticorps bap-135, anticorps bap135, anticorps btkap1, anticorps diws, anticorps gtfii-i, anticorps ib291, anticorps spin, anticorps tfii-i, anticorps wbs, anticorps wbscr6, anticorps gtf2i, anticorps gtf2i.L, anticorps general transcription factor IIi, anticorps general transcription factor II I, anticorps general transcription factor IIi S homeolog, anticorps GTF2I, anticorps Gtf2i, anticorps gtf2i, anticorps gtf2i.S

Sujet: This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed.

Poids moléculaire:

Observed_MW: 132 kDa

Calculated_MW: 30 kDa/107 kDa/110 kDa/112 kDa

ID gène: 2969

UniProt: P78347