FOXC1 anticorps

N° du produit ABIN7244225

Détail du produit anti-FOXC1 anticorps

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FOXC1 est non-conjugé

Application: Western Blotting (WB), ELISA

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Synthetic peptide of human FOXC1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000, ELISA 1:2000-5000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.1 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur FOXC1

Antigène: FOXC1 (Forkhead Box C1 (FOXC1))

Autre désignation: FOXC1 (FOXC1 Produits)

Synonymes: anticorps ARA, anticorps FKHL7, anticorps FREAC-3, anticorps FREAC3, anticorps IGDA, anticorps IHG1, anticorps IRID1, anticorps RIEG3, anticorps FoxC1, anticorps fkhl7, anticorps freac-3, anticorps freac3, anticorps igda, anticorps ihg1, anticorps irid1, anticorps rieg3, anticorps xfd-11, anticorps ara, anticorps FOXC1, anticorps foxc1, anticorps Fkh1, anticorps Mf1, anticorps Mf4, anticorps ch, anticorps fkh-1, anticorps frkhda, anticorps CFKH-1, anticorps XFD-11, anticorps foxc1.2, anticorps id:ibd5079, anticorps forkhead box C1, anticorps forkhead box C1 S homeolog, anticorps forkhead box C1 L homeolog, anticorps Forkhead box protein C1, anticorps winged helix transcription factor XFD-11, anticorps forkhead box C1b, anticorps FOXC1, anticorps Foxc1, anticorps foxc1.S, anticorps foxc1, anticorps foxc1.L, anticorps foxc1-A, anticorps foxc1b

Sujet: 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.

Poids moléculaire: 57 kDa

NCBI Accession: NP_001444

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process