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Coagulation Factor IX anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement Coagulation Factor IX dans ELISA. Il présente une réactivité envers Humain.
N° du produit ABIN7670576

Aperçu rapide pour Coagulation Factor IX anticorps (ABIN7670576)

Antigène

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

Reactivité

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

Hôte

  • 75
  • 22
  • 9
  • 8
  • 4
  • 1
  • 1
Lapin

Clonalité

  • 96
  • 23
Polyclonal

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

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

    Purification

    Antigen Affinity Purification

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Sterile PBS , pH 7.4

    Agent conservateur

    Without preservative

    Conseil sur la manipulation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

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

    Date de péremption

    12 months
  • Antigène

    Coagulation Factor IX (F9)

    Autre désignation

    F9

    Sujet

    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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