FOXC1 anticorps (Internal Region)

N° du produit ABIN569579

L’anticorps anti-FOXC1 Polyclonal Chèvre est utilisé pour la détection de FOXC1 dans des échantillons de Humain, Souris et Porc. Il a été validé pour WB et EIA.

Aperçu rapide pour FOXC1 anticorps (Internal Region) (ABIN569579)

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Reactivité: Humain, Souris, Porc

Hôte: Chèvre

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXC1 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-FOXC1 anticorps

Épitope: Internal Region

Séquence: C-DAVKDKEEKD RLH

Specificité: Recognizes FOXC1 (internal).

Réactivité croisée (Details): Species reactivity (expected):Pig, Mouse.
Species reactivity (tested):Human.

Purification: Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide.

Immunogène: Dynthetic peptide from an internal region of Human FOXC1 (NP_001444.2). Genename: FOXC1

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Concentration: 0.5 mg/mL

Buffer: Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer.

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur FOXC1

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Autre désignation: FOXC1 / FKHL7 / FREAC3

Sujet: FOXC1 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.Synonyms: FREAC-3, Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3

Poids moléculaire: 56.8kDa (NP_001444.2).

ID gène: 2296

NCBI Accession: NP_001444

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process