Coagulation Factor IX Antikörper

Produktnummer ABIN452591

Der Maus Monoklonal Anti-Coagulation Factor IX-Antikörper wurde für EIA validiert. Er ist geeignet, Coagulation Factor IX in Proben von Human zu detektieren.

Kurzübersicht für Coagulation Factor IX Antikörper (ABIN452591)

Target: Coagulation Factor IX (F9)

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser Coagulation Factor IX Antikörper ist unkonjugiert

Applikation: Enzyme Immunoassay (EIA)

Klon: F9-1

Produktdetails anti-Coagulation Factor IX Antikörper

Spezifität: Human Factor IX.

Kreuzreaktivität (Details): Species reactivity (tested):Human.

Produktmerkmale: Synonyms: Christmas factor, PTC, Plasma thromboplastin component

Aufreinigung: Affinity Chromatography on Protein G.

Immunogen: Human Factor IX.

Isotyp: IgG1

Anwendungsinformationen

Applikationshinweise: ELISA.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Rekonstitution: Restore with Double distillated water to a final concentration of 1.0 mg/mL.

Buffer: 0.01 M PBS, pH 7.2 without preservatives.

Konservierungsmittel: Without preservative

Lagerung: -20 °C

Informationen zur Lagerung: Store the antibody (in aliquots) at -20 °C. Avoid repeated freezing and thawing.
Shelf life: one year from despatch.

Haltbarkeit: 12 months

Details zu Coagulation Factor IX

Target: Coagulation Factor IX (F9)

Hintergrund: Factor IX circulates in the blood as an inactive zymogen at the normal concentration of approximately 3 μg/mL. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca2+ ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X linked disorder, also called hemophilia B or Christmas disease. The disease affects approximately 1 in 50,000 of the population (almost exclusively males).Synonyms: Christmas factor, PTC, Plasma thromboplastin component

Gen-ID: 2158

UniProt: P00740