FOXC1 Antikörper (Internal Region)

Produktnummer ABIN569579

Der Ziege Polyklonal anti-FOXC1 Antikörper wird verwendet zum Nachweis von FOXC1 in Proben von Human, Maus und Schwein. Er wurde validiert für WB und EIA.

Kurzübersicht für FOXC1 Antikörper (Internal Region) (ABIN569579)

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Reaktivität: Human, Maus, Schwein

Wirt: Ziege

Klonalität: Polyklonal

Konjugat: Dieser FOXC1 Antikörper ist unkonjugiert

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

Produktdetails anti-FOXC1 Antikörper

Bindungsspezifität: Internal Region

Sequenz: C-DAVKDKEEKD RLH

Spezifität: Recognizes FOXC1 (internal).

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

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

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

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 0.5 mg/mL

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

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

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

Details zu FOXC1

Target: FOXC1 (Forkhead Box C1 (FOXC1))

Andere Bezeichnung: FOXC1 / FKHL7 / FREAC3

Hintergrund: 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

Molekulargewicht: 56.8kDa (NP_001444.2).

Gen-ID: 2296

NCBI Accession: NP_001444

UniProt: Q12948

Pathways: Chromatin Binding, Glycosaminoglycan Metabolic Process