FOXC1 anticorps (AA 392-554) (FITC)

N° du produit ABIN7991375

Cet anticorps anti-FOXC1 Polyclonal Lapin conjugué à FITC (ABIN7991375) détecte spécifiquement FOXC1 dans FACS. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour FOXC1 anticorps (AA 392-554) (FITC) (ABIN7991375)

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXC1 est conjugé à/à la FITC

Application: Flow Cytometry (FACS)

Détail du produit anti-FOXC1 anticorps (FITC)

Épitope: AA 392-554

Fonction: Anti-FOXC1 Antibody FITC Conjugated

Specificité: No cross reactivity with other proteins.

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

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human FOXC1 recombinant protein (Position: T392-F554).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

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: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur FOXC1

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Autre désignation: FOXC1

Sujet:

Background: Forkhead box C1, also known as?FOXC1, is a?protein?which in humans is encoded by the?FOXC1?gene. It is mapped to 6p25.3. This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.

Gene Full Name: forkhead box C1

ID gène: 2296

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process