Coagulation Factor IX Antikörper

Produktnummer ABIN951594

Produktdetails anti-Coagulation Factor IX Antikörper

Target: Coagulation Factor IX (F9)

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser Coagulation Factor IX Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Spezifität: Recognises Factor IX

Aufreinigung: Protein G Chromatography

Immunogen: Full length native protein (purified) (Human).

Klon: 13F42-F6

Isotyp: IgG1

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 3.5 mg/mL

Buffer: 0.05 M Sodium Phosphate, 0.5 M NaCl, 1 mM EDTA, pH 6.6

Handhabung: Avoid repeated freezing and thawing.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -70 °C.

Details zu Coagulation Factor IX

Target: Coagulation Factor IX (F9)

Abstract: F9 Produkte

Synonyme: AA407498 antikoerper, AI506714 antikoerper, AK-3 antikoerper, Ak3l antikoerper, Ak3l1 antikoerper, Akl3l antikoerper, FIX antikoerper, HEMB antikoerper, P19 antikoerper, PTC antikoerper, THPH8 antikoerper, AW111646 antikoerper, Cf-9 antikoerper, Cf9 antikoerper, f9 antikoerper, zgc:109775 antikoerper, fix antikoerper, ptc antikoerper, hemb antikoerper, FIXA antikoerper, zgc:136807 antikoerper, adenylate kinase 3 antikoerper, coagulation factor IX antikoerper, coagulation factor IXa antikoerper, coagulation factor 9 antikoerper, coagulation factor 9 S homeolog antikoerper, Coagulation factor IX antikoerper, coagulation factor IXb antikoerper, Ak3 antikoerper, F9 antikoerper, f9a antikoerper, f9 antikoerper, CpipJ_CPIJ003776 antikoerper, CpipJ_CPIJ009129 antikoerper, CpipJ_CPIJ013063 antikoerper, CpipJ_CPIJ013624 antikoerper, Tsp_01441 antikoerper, f9.S antikoerper, fa9 antikoerper, f9b antikoerper

Hintergrund: Coagulation Factor IX (F9) circulates in the blood as an inactive zymogen. 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 Ca+2 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.Synonyms: Christmas factor, PTC, Plasma thromboplastin component

Gen-ID: 2158

NCBI Accession: NP_000124

UniProt: P00740