HES7 anticorps

N° du produit ABIN5027717

Détail du produit anti-HES7 anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HES7 est non-conjugé

Application: Western Blotting (WB)

Purification: Protein A Chromatography

Immunogène: Full length recombinant Hes7 protein was used as the immunogen for this antibody.

Isotype: IgG

Information d'application

Indications d'application: WB: 0.5-1 μg/mL

Restrictions: For Research Use only

Stockage

Concentration: 0.5 mg/mL

Buffer: PBS containing 0.05 % BSA, PH 7.4

Agent conservateur: Sodium azide

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

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.

Détails sur HES7

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

Autre désignation: Hes7 (HES7 Produits)

Synonymes: anticorps SCDO4, anticorps bHLHb37, anticorps hes family bHLH transcription factor 7, anticorps hairy and enhancer of split 7 (Drosophila), anticorps HES7, anticorps Hes7

Sujet: HES7 (Hes family bHLH transcription factor 7) is a member of the Hairy-and-enhancer-of-split (HES) family of transcription factors, which play a role in somite formation. This is expressed in an oscillatory manner during the process of somitogenesis, a process by which somites (bilaterally paired blocks of mesoderm) form and give rise to skeletal muscle, cartilage, tendons, endothelial cells, and dermis. Missense mutations of HES7 have been reported to cause SCDO4 (Spondylocostal Dysostosis 4), an inherited disorder that is characterized by the presence of extensive hemivertebrae, truncal shortening and abnormally aligned ribs.

Poids moléculaire: 25 kDa

ID gène: 84667

UniProt: Q9BYE0