FOXI1 anticorps

N° du produit ABIN2458351

Cet anticorps Lapin Polyclonal détecte spécifiquement FOXI1 dans WB et ELISA. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour FOXI1 anticorps (ABIN2458351)

Antigène: FOXI1 (Forkhead Box I1 (FOXI1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXI1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-FOXI1 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 FOXI1.

Information d'application

Indications d'application: FOXI1 antibody can be used for detection of FOXI1 by ELISA at 1:62500. FOXI1 antibody can be used for detection of FOXI1 by western blot at 1 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 FOXI1 antibody at -20 °C.

Détails sur FOXI1

Antigène: FOXI1 (Forkhead Box I1 (FOXI1))

Autre désignation: FOXI1

Sujet: FOXI1 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. FOXI1 may plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis.This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined, however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene.

Poids moléculaire: 41 kDa

ID gène: 2299

NCBI Accession: NP_036320

UniProt: Q12951