Coagulation Factor IX Antikörper
-
- Target Alle Coagulation Factor IX (F9) Antikörper anzeigen
- Coagulation Factor IX (F9)
-
Reaktivität
- Human, Maus, Ratte
-
Wirt
- Kaninchen
-
Klonalität
- Polyklonal
-
Konjugat
- Dieser Coagulation Factor IX Antikörper ist unkonjugiert
-
Applikation
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human Coagulation factor IXa heavy chain
- Isotyp
- IgG
- Top Product
- Discover our top product F9 Primärantikörper
-
-
- Applikationshinweise
-
WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Haltbarkeit
- 12 months
-
-
Surface functionalization-specific binding of coagulation factors by zinc oxide nanoparticles delays coagulation time and reduces thrombin generation potential in vitro." in: PLoS ONE, Vol. 12, Issue 7, pp. e0181634, (2017) (PubMed).
: "
-
Surface functionalization-specific binding of coagulation factors by zinc oxide nanoparticles delays coagulation time and reduces thrombin generation potential in vitro." in: PLoS ONE, Vol. 12, Issue 7, pp. e0181634, (2017) (PubMed).
-
- Target
- Coagulation Factor IX (F9)
- Andere Bezeichnung
- Factor 9 (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
-
Synonyms: Christmas Disease, Christmas factor, Coagulant factor IX, Coagulation factor 9, Coagulation factor IX plasma thromboplastic component, Coagulation factor IX, Coagulation factor IXa heavy chain, F9, FA9_HUMAN, Factor 9, Factor IX Deficiency, Factor9, FactorIX, FIX, GLA domain, Haemophilia B, MGC129641, MGC129642, P19 antibody Plasma thromboplastic component, Plasma thromboplastin component, PTC, Truncated coagulation factor IX.
Background: Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (prothrombin, and factors X, IX, V, and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble fibrin clots and the promotion of platelet aggregation (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).
- Gen-ID
- 2158
-