GTF2I anticorps (C-Term)

N° du produit ABIN453078

Cet anticorps anti-GTF2I est un anticorps Lapin Polyclonal détectant GTF2I dans WB et EIA. Adapté pour Humain.

Aperçu rapide pour GTF2I anticorps (C-Term) (ABIN453078)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GTF2I est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-GTF2I anticorps

Épitope: C-Term

Specificité: This antibody detects GTF2I / TFII-I at C-term.

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Purified through a protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide selected from the C-terminal region of human GTF2I

Information d'application

Indications d'application: Western blot: 1: 100 - 1: 500. ELISA: 1: 1,000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: 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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer.

Détails sur GTF2I

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

Autre désignation: GTF2I / TFII-I

Sujet: GTF2I is 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.Synonyms: BAP-135, BAP135, Bruton tyrosine kinase-associated protein 135, GTFII-I, General transcription factor II-I, SPIN, SRF-Phox1-interacting protein, WBSCR6, Williams-Beuren syndrome chromosomal region 6 protein

Poids moléculaire: 112416 Da

ID gène: 2969

NCBI Accession: NP_001509

UniProt: P78347