FOXP2 anticorps

N° du produit ABIN2460798

Cet anticorps anti-FOXP2 est un anticorps Lapin Polyclonal détectant FOXP2 dans WB et ELISA. Adapté pour Humain, Rat et Chien.

Aperçu rapide pour FOXP2 anticorps (ABIN2460798)

Antigène: FOXP2 (Forkhead Box P2 (FOXP2))

Reactivité: Humain, Rat, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXP2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-FOXP2 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 FOXP2.

Information d'application

Indications d'application: FOXP2 antibody can be used for detection of FOXP2 by ELISA at 1:62500. FOXP2 antibody can be used for detection of FOXP2 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 FOXP2 antibody at -20 °C.

Détails sur FOXP2

Antigène: FOXP2 (Forkhead Box P2 (FOXP2))

Autre désignation: FOXP2

Sujet: FOXP2 is an evolutionarily conserved transcription factor expressed in fetal and adult brain. This transcription factor is a member of the forkhead/winged-helix (FOX) family of transcription factors, and contains a FOX DNA-binding domain and a large polyglutamine tract. Members of the FOX family of transcription factors are regulators of embryogenesis. The product of this gene is thought to be required for proper development of speech and language regions of the brain during embryogenesis. Although a point mutation in this gene has been associated with the KE pedigree segregating developmental verbal dyspraxia, no association between mutations in this gene and another speech disorder, autism, has been found. Four alternative transcripts encoding three different isoforms have been identified.

Poids moléculaire: 80 kDa, 83 kDa

ID gène: 93986

NCBI Accession: NP_055306

UniProt: O15409