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Coagulation Factor IX Antikörper

Dieses Anti-Coagulation Factor IX-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von Coagulation Factor IX in WB, IHC (p) und EIA. Geeignet für Human.
Produktnummer ABIN951594

Kurzübersicht für Coagulation Factor IX Antikörper (ABIN951594)

Target

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

Reaktivität

  • 100
  • 37
  • 31
  • 9
  • 8
  • 2
  • 1
  • 1
Human

Wirt

  • 83
  • 25
  • 9
  • 8
  • 4
  • 1
  • 1
Maus

Klonalität

  • 103
  • 27
Monoklonal

Konjugat

  • 76
  • 15
  • 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

  • 100
  • 48
  • 45
  • 31
  • 28
  • 13
  • 8
  • 8
  • 7
  • 7
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Klon

13F42-F6
  • Spezifität

    Recognises Factor IX

    Aufreinigung

    Protein G Chromatography

    Immunogen

    Full length native protein (purified) (Human).

    Isotyp

    IgG1
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • 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.
  • Target

    Coagulation Factor IX (F9)

    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
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