FOXC1 Antikörper

Produktnummer ABIN7244225

Produktdetails anti-FOXC1 Antikörper

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FOXC1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Synthetic peptide of human FOXC1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-2000, ELISA 1:2000-5000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.1 mg/mL

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

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu FOXC1

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Andere Bezeichnung: FOXC1 (FOXC1 Produkte)

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

Hintergrund: 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.

Molekulargewicht: 57 kDa

NCBI Accession: NP_001444

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process