ATOH7 antibody (AA 31-120) (HRP)

Catalog No. ABIN6987611

The Rabbit Polyclonal anti-ATOH7 antibody has been validated for WB, ELISA, IHC (p) and IHC (fro). It is suitable to detect ATOH7 in samples from Mouse.

Quick Overview for ATOH7 antibody (AA 31-120) (HRP) (ABIN6987611)

Target: ATOH7 (Atonal Homolog 7 (ATOH7))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ATOH7 antibody is conjugated to HRP

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

Product Details anti-ATOH7 Antibody (HRP)

Binding Specificity: AA 31-120

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human MAT2A

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for ATOH7

Target: ATOH7 (Atonal Homolog 7 (ATOH7))

Alternative Name: MATH5

Background:

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]

Gene ID: 220202

UniProt: Q8N100