HES7 anticorps (AA 26-172)

N° du produit ABIN7995965

Cet anticorps anti-HES7 Polyclonal Lapin (ABIN7995965) détecte spécifiquement HES7 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour HES7 anticorps (AA 26-172) (ABIN7995965)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HES7 est non-conjugé

Application: Western Blotting (WB), ELISA

Classe de qualité: Carrier-free

Détail du produit anti-HES7 anticorps

Épitope: AA 26-172

Fonction: Anti-HES7 Antibody

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human HES7 shares 92.5% amino acid (aa) sequence identity with mouse HES7.

Attributs du produit: Anti-HES7 Antibody. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogène: 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

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

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.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Date de péremption: 12 months

Détails sur HES7

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

Autre désignation: HES7

Sujet:

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.

Gene Full Name: hes family bHLH transcription factor 7

Poids moléculaire: 25 kDa

ID gène: 84667

UniProt: Q9BYE0