GTF2IRD2 anticorps (full length)

N° du produit ABIN7878330

L’anticorps anti-GTF2IRD2 Monoclonal Souris est utilisé pour la détection de GTF2IRD2 dans des échantillons de Humain. Il a été validé pour WB et FACS.

Aperçu rapide pour GTF2IRD2 anticorps (full length) (ABIN7878330)

Antigène: GTF2IRD2 (GTF2I Repeat Domain Containing 2 (GTF2IRD2))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp GTF2IRD2 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS)

Classe de qualité: Carrier-free

Clone: PCRP-GTF2IRD2-1B12

Détail du produit anti-GTF2IRD2 anticorps

Épitope: full length

Fonction: GTF2IRD2 alpha Antibody / GTF2IRD2 (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: Recombinant full-length human General transcription factor II-I repeat domain-containing protein 2A protein was used as the immunogen for the GTF2IRD2 alpha antibody.

Isotype: IgG2b

Information d'application

Indications d'application: Optimal dilution of the GTF2IRD2 alpha antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: -20 °C

Stockage commentaire: Aliquot the GTF2IRD2 alpha antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur GTF2IRD2

Antigène: GTF2IRD2 (GTF2I Repeat Domain Containing 2 (GTF2IRD2))

Autre désignation: GTF2IRD2 alpha

Sujet: The TFII-I family contains two highly homologous 949 amino acid proteins, GTF2IRD2 (also called GTF2IRD2 alpha and GTF2IRD2A) and GTF2IRD2B. Localizing to the nucleus, these proteins are ubiquitously expressed and contain two GTF2I- like repeats. Encoded by a gene mapping to human chromosome 7q11.23, GTF2IRD2 and GTF2IRD2B are located in the Williams-Beuren syndrome (WBS) critical region. The deletion of genes located within this region results in WBS, possibly due to the unequal crossing over of highly homologous low-copy repeat sequences that flank the deleted region. WBS is an autosomal dominant genetic condition that is characterized by physical, cognitive and behavioral traits including facial dysmorphology, vascular stenoses, growth deficiencies, dental anomalies and neurologic and musculoskeletal abnormalities.

UniProt: Q86UP8