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Coagulation Factor IX anticorps

L’anticorps Souris Monoclonal anti-Coagulation Factor IX a été validé pour EIA. Il convient pour détecter Coagulation Factor IX dans des échantillons de Humain.
N° du produit ABIN452591

Aperçu rapide pour Coagulation Factor IX anticorps (ABIN452591)

Antigène

Voir toutes Coagulation Factor IX (F9) Anticorps
Coagulation Factor IX (F9)

Reactivité

  • 95
  • 35
  • 30
  • 8
  • 7
  • 1
  • 1
  • 1
Humain

Hôte

  • 76
  • 21
  • 9
  • 8
  • 4
  • 1
  • 1
Souris

Clonalité

  • 97
  • 22
Monoclonal

Conjugué

  • 66
  • 14
  • 9
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Coagulation Factor IX est non-conjugé

Application

  • 91
  • 44
  • 39
  • 23
  • 21
  • 13
  • 8
  • 8
  • 7
  • 7
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Enzyme Immunoassay (EIA)

Clone

F9-1
  • Specificité

    Human Factor IX.

    Réactivité croisée (Details)

    Species reactivity (tested):Human.

    Attributs du produit

    Synonyms: Christmas factor, PTC, Plasma thromboplastin component

    Purification

    Affinity Chromatography on Protein G.

    Immunogène

    Human Factor IX.

    Isotype

    IgG1
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Reconstitution

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

    Buffer

    0.01 M PBS, pH 7.2 without preservatives.

    Agent conservateur

    Without preservative

    Stock

    -20 °C

    Stockage commentaire

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

    Date de péremption

    12 months
  • Antigène

    Coagulation Factor IX (F9)

    Sujet

    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

    ID gène

    2158

    UniProt

    P00740
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