ATOH7 anticorps (AA 31-120) (Biotin)

N° du produit ABIN6982690

Cet anticorps Lapin Polyclonal détecte spécifiquement ATOH7 dans WB, ELISA, IHC (p) et IHC (fro). Il présente une réactivité envers Souris.

Aperçu rapide pour ATOH7 anticorps (AA 31-120) (Biotin) (ABIN6982690)

Antigène: ATOH7 (Atonal Homolog 7 (ATOH7))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ATOH7 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-ATOH7 anticorps (Biotin)

Épitope: AA 31-120

Réactivité croisée: Souris

Homologie: Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human MAT2A

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur ATOH7

Antigène: ATOH7 (Atonal Homolog 7 (ATOH7))

Autre désignation: MATH5

Sujet:

Synonyms: ATOH7, ATOH7_HUMAN, Atonal homolog 7 (Drosophila), Atonal Homolog 7, bHLHa13, Class A basic helix-loop-helix protein 13, hATH5, Helix-loop-helix protein hATH-5, Math5, Protein atonal homolog 7.

Background: This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Studies in mice suggest that this gene plays a central role in retinal ganglion cell and optic nerve formation. Mutations in this gene are associated with nonsyndromic congenital retinal nonattachment. [provided by RefSeq, Dec 2011]

ID gène: 220202

UniProt: Q8N100