Recombinant SOX17 anticorps

N° du produit ABIN7828584

Cet anticorps anti-SOX17 Monoclonal Lapin (Clone A676) (ABIN7828584) détecte spécifiquement SOX17 dans WB et IHC. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour Recombinant SOX17 anticorps (ABIN7828584)

Antigène: SOX17 (SRY (Sex Determining Region Y)-Box 17 (SOX17))

Type d'anticorp: Recombinant Antibody

Reactivité: Humain

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp SOX17 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Clone: A676

Détail du produit anti-SOX17 anticorps

Fonction: Recombinant SOX17 Monoclonal Antibody

Purification: Protein A purified

Immunogène: Recombinant human SOX17 fragment

Isotype: IgG, kappa

Information d'application

Indications d'application: WB 1:1000-1:2000,IHC 1:100-1:200

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

Agent conservateur: ProClin

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

Stock: -20 °C

Stockage commentaire: Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Date de péremption: 12 months

Détails sur SOX17

Antigène: SOX17 (SRY (Sex Determining Region Y)-Box 17 (SOX17))

Autre désignation: SOX17

Sujet: VUR,SOX,VUR3,SOX17,SRY-related high mobility group box (SOX) proteins comprise a large family of widely conserved transcription factors. SOX proteins do not directly mediate transcription, but require binding partners that regulate their ability to mediate transcription of target genes that control cell fate determination and development .Transcription factor Sox17 is a Sox family protein with an established role in endoderm specification during development. In addition, Sox17 plays essential roles in the maintenance of the hematopoietic stem cell pool and for vascular morphogenesis during development. Sox17 negatively regulates oligodendrocyte precursor differentiation by antagonizing β-catenin signaling. Mutation in the correspondingSox17gene in humans is associated with a form of vesicoureteral reflux, a disorder characterized by congenital kidney and urinary tract defects. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

Poids moléculaire:

Calculated MW: 55 kDa

Observed MW: 55 kDa

UniProt: Q9H6I2