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Coagulation Factor IX anticorps (AA 217-423)

Cet anticorps Lapin Polyclonal détecte spécifiquement Coagulation Factor IX dans WB et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN1886209

Aperçu rapide pour Coagulation Factor IX anticorps (AA 217-423) (ABIN1886209)

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

  • 90
  • 44
  • 38
  • 23
  • 21
  • 13
  • 8
  • 8
  • 7
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Épitope

    • 7
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 217-423

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 217 and 423 of Human F9
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.100-1.250

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 20 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    Coagulation Factor IX (F9)

    Autre désignation

    Factor IX

    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.[provided by RefSeq]

    Poids moléculaire

    52 kDa

    ID gène

    2158
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