GTF2I anticorps

N° du produit ABIN2460315

Cet anticorps anti-GTF2I est un anticorps Lapin Polyclonal détectant GTF2I dans WB, IHC et ELISA. Adapté pour Humain, Souris et Chien.

Aperçu rapide pour GTF2I anticorps (ABIN2460315)

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

Reactivité: Humain, Souris, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GTF2I est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-GTF2I anticorps

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GTF2I.

Information d'application

Indications d'application: GTF2I antibody can be used for detection of GTF2I by ELISA at 1:62500. GTF2I antibody can be used for detection of GTF2I by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store GTF2I antibody at -20 °C.

Détails sur GTF2I

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

Autre désignation: GTF2I

Sujet: GTF2I encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon (s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.

Poids moléculaire: 110 kDa

ID gène: 2969

NCBI Accession: NP_127493

UniProt: Q75M86