ATOH7 antibody

Catalog No. ABIN7227406

The Rabbit Polyclonal anti-ATOH7 antibody is suitable to detect ATOH7 in samples from Human and Mouse. It has been validated for WB and ELISA.

Quick Overview for ATOH7 antibody (ABIN7227406)

Target: ATOH7 (Atonal Homolog 7 (ATOH7))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ATOH7 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-ATOH7 Antibody

Purpose: Rabbit Anti-ATOH7 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of ATOH7 protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from part region of human ATOH7 protein

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for ATOH7

Target: ATOH7 (Atonal Homolog 7 (ATOH7))

Alternative Name: ATOH7

Background: Protein atonal homolog 7, Class A basic helix-loop-helix protein 13, bHLHa13, Helix-loop-helix protein hATH-5, hATH5This 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.

Molecular Weight: 16kD

Gene ID: 220202

UniProt: Q8N100