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Coagulation Factor IX Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch Coagulation Factor IX in ELISA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7670576

Kurzübersicht für Coagulation Factor IX Antikörper (ABIN7670576)

Target

Alle Coagulation Factor IX (F9) Antikörper anzeigen
Coagulation Factor IX (F9)

Reaktivität

  • 95
  • 35
  • 30
  • 8
  • 7
  • 1
  • 1
  • 1
Human

Wirt

  • 75
  • 22
  • 9
  • 8
  • 4
  • 1
  • 1
Kaninchen

Klonalität

  • 96
  • 23
Polyklonal

Konjugat

  • 66
  • 14
  • 9
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Coagulation Factor IX Antikörper ist unkonjugiert

Applikation

  • 91
  • 43
  • 39
  • 23
  • 21
  • 13
  • 8
  • 8
  • 7
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA
  • Verwendungszweck

    Factor IX/PTC/F9 Polyclonal Antibody(Capture/Detector)

    Aufreinigung

    Antigen Affinity Purification

    Immunogen

    Recombinant Human Factor IX/PTC/F9 protein expressed by Mammalian

    Isotyp

    IgG
  • Applikationshinweise

    ELISA Capture 2-8 μg/mL,ELISA Detector 0.1-0.4 μg/mL

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1 mg/mL

    Buffer

    Sterile PBS , pH 7.4

    Konservierungsmittel

    Without preservative

    Handhabung

    Avoid freeze / thaw cycles. This preparation contains no preservatives, thus it should be handled under aseptic conditions.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store at 4°C Valid for 1 month or -20°C Valid for 12 months

    Haltbarkeit

    12 months
  • Target

    Coagulation Factor IX (F9)

    Andere Bezeichnung

    F9

    Hintergrund

    HEMB,P19,PTC,THPH8,Christmas Factor,This gene encodes vitamin K-dependent coagulation factor IX that 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.

    UniProt

    P00740
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