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Coagulation Factor IX anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement Coagulation Factor IX dans WB et IF. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7258664

Aperçu rapide pour Coagulation Factor IX anticorps (ABIN7258664)

Antigène

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

Reactivité

  • 94
  • 34
  • 29
  • 8
  • 7
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 74
  • 22
  • 9
  • 8
  • 4
  • 1
  • 1
Lapin

Clonalité

  • 95
  • 23
Polyclonal

Conjugué

  • 65
  • 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

  • 90
  • 43
  • 39
  • 23
  • 21
  • 13
  • 8
  • 8
  • 7
  • 7
  • 6
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human Factor IX / F9 (NP_000124.1).

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    Coagulation Factor IX (F9)

    Autre désignation

    Factor IX / F9

    Sujet

    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. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.

    Poids moléculaire

    Observed_MW: 50 kDa

    Calculated_MW: 47 kDa/51 kDa

    ID gène

    2158

    UniProt

    P00740
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