FOXC1 anticorps (AA 392-554)

N° du produit ABIN7874618

Cet anticorps Lapin Polyclonal détecte spécifiquement FOXC1 dans WB, ELISA et IF. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour FOXC1 anticorps (AA 392-554) (ABIN7874618)

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXC1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF)

Détail du produit anti-FOXC1 anticorps

Épitope: AA 392-554

Fonction: FOXC1 Antibody

Purification: Affinity purified

Immunogène: A human recombinant protein (amino acids T392-F554) was used as the immunogen for the FOXC1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the FOXC1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the FOXC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur FOXC1

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Autre désignation: FOXC1

Sujet: 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.

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process