HES7 antibody (AA 26-172)

Catalog No. ABIN7825440

This Rabbit Polyclonal antibody specifically detects HES7 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for HES7 antibody (AA 26-172) (ABIN7825440)

Target: HES7 (Hairy and Enhancer of Split 7 (HES7))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HES7 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-HES7 Antibody

Binding Specificity: AA 26-172

Purpose: Anti-HES7 Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Characteristics: Anti-HES7 Antibody catalog # A06494-1. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human HES7 recombinant protein (Position: D26-R172). Human HES7 shares 92.5% amino acid (aa) sequence identity with mouse HES7.

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Storage: 4 °C,-20 °C

Storage Comment: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Target Details for HES7

Target: HES7 (Hairy and Enhancer of Split 7 (HES7))

Alternative Name: HES7

Background: This gene encodes a member of the hairy and enhancer of split family of bHLH transcription factors. The mouse ortholog of this gene is regulated by Notch signaling. The protein functions as a transcriptional repressor, and is implicated in correct patterning of the axial skeleton. A mutation in this gene has been shown to result in spondylocostal dysostosis. Multiple transcript variants encoding different isoforms have been found for this gene.

Molecular Weight: 25 kDa

Gene ID: 84667