FOXP2 anticorps (AA 657-684)

N° du produit ABIN1539974

L’anticorps Souris Monoclonal anti-FOXP2 a été validé pour WB. Il convient pour détecter FOXP2 dans des échantillons de Humain.

Aperçu rapide pour FOXP2 anticorps (AA 657-684) (ABIN1539974)

Antigène: FOXP2 (Forkhead Box P2 (FOXP2))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp FOXP2 est non-conjugé

Application: Western Blotting (WB)

Clone: 533CT26-1-2

Détail du produit anti-FOXP2 anticorps

Épitope: AA 657-684

Homologie: M, Rat

Purification: Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.

Immunogène: This FOXP2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 657-684 amino acids from human FOXP2.

Isotype: IgM

Information d'application

Indications d'application: WB: 1:100~1600

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Mouse monoclonal antibody supplied in crude ascites 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.

Stock: 4 °C,-20 °C

Stockage commentaire: FOXP2 Antibody(Ascites) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur FOXP2

Antigène: FOXP2 (Forkhead Box P2 (FOXP2))

Autre désignation: FOXP2

Sujet: This gene encodes a member of the forkhead/winged-helix (FOX) family of transcription factors. It is expressed in fetal and adult brain as well as in several other organs such as the lung and gut. The protein product contains a FOX DNA-binding domain and a large polyglutamine tract and is an evolutionarily conserved transcription factor, which may bind directly to approximately 300 to 400 gene promoters in the human genome to regulate the expression of a variety of genes. This gene is required for proper development of speech and language regions of the brain during embryogenesis, and may be involved in a variety of biological pathways and cascades that may ultimately influence language development. Mutations in this gene cause speech-language disorder 1 (SPCH1), also known as autosomal dominant speech and language disorder with orofacial dyspraxia. Multiple alternative transcripts encoding different isoforms have been identified in this gene.

Poids moléculaire: 79919

ID gène: 93986

NCBI Accession: NP_001166237, NP_001166238, NP_055306, NP_683696, NP_683697, NP_683698

UniProt: O15409