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VWF anticorps (AA 1287-2770)

L’anticorps Lapin Polyclonal anti-VWF a été validé pour IHC et ELISA. Il convient pour détecter VWF dans des échantillons de Humain.
N° du produit ABIN7599909

Aperçu rapide pour VWF anticorps (AA 1287-2770) (ABIN7599909)

Antigène

Voir toutes VWF Anticorps
VWF (Von Willebrand Factor (VWF))

Reactivité

  • 191
  • 38
  • 28
  • 7
  • 6
  • 5
  • 1
  • 1
Humain

Hôte

  • 106
  • 104
  • 13
  • 7
  • 1
  • 1
  • 1
Lapin

Clonalité

  • 129
  • 99
  • 2
Polyclonal

Conjugué

  • 104
  • 25
  • 15
  • 7
  • 7
  • 7
  • 7
  • 7
  • 7
  • 7
  • 6
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp VWF est non-conjugé

Application

  • 139
  • 139
  • 77
  • 61
  • 57
  • 45
  • 31
  • 28
  • 25
  • 16
  • 16
  • 15
  • 9
  • 9
  • 7
  • 6
  • 6
  • 5
  • 5
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Épitope

    • 53
    • 21
    • 16
    • 10
    • 7
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1287-2770

    Fonction

    Anti-Von Willebrand Factor/VWF Antibody

    Réactivité croisée (Details)

    No cross-reactivity with other proteins.

    Attributs du produit

    Anti-Von Willebrand Factor/VWF Antibody Picoband® (ABIN7599909). Tested in ELISA, IHC applications. This antibody reacts with Human.

    Purification

    Immunogen affinity purified.

    Immunogène

    E.coli-derived human Von Willebrand Factor/VWF recombinant protein (Position: R1287-Q2770).

    Isotype

    IgG
  • Indications d'application

    Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Sadler JE (1998). "Biochemistry and genetics of von Willebrand factor". Annu. Rev. Biochem. 67: 395-424. 2. Ginsburg, D., Handin, R. I., Bonthron, D. T., Donlon, T. A., Bruns, G. A. P., Latt, S. A., Orkin, S. H. Human von Willebrand factor (VWF): isolation of complementary DNA (cDNA) clones and chromosomal localization. Science 228: 1401-1406, 1985. 3. Sporn, L. A., Marder, V. J., Wagner, D. D. Von Willebrand factor released from Weibel-Palade bodies binds more avidly to extracellular matrix than that secreted constitutively. Blood 69: 1531-1534, 1987.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Antigène

    VWF (Von Willebrand Factor (VWF))

    Autre désignation

    VWF

    Sujet

    Synonyms: Hepatocyte nuclear factor 3-alpha, HNF-3-alpha, HNF-3A, Forkhead box protein A1, Transcription factor 3A, TCF-3A, FOXA1, HNF3A, TCF3A

    Tissue Specificity: Highly expressed in prostate and ESR1-positive breast tumors. Overexpressed in esophageal and lung adenocarcinomas.

    Background: Von Willebrand factor (VWF) is a blood glycoprotein involved in hemostasis. It is mapped to 12p13.31. The VWF gene encodes von Willebrand factor (VWF), a large multimeric glycoprotein that plays a central role in the blood coagulation system, serving both as a major mediator of platelet-vessel wall interaction and platelet adhesion, and as a carrier for coagulation factor VIII. VWF released from endothelial cell Weibel-Palade bodies bound particularly avidly to the extracellular matrix. VWF deficiency or dysfunction (von Willebrand disease) leads to a bleeding tendency, which is most apparent in tissues having high blood flow shear in narrow vessels.

    Poids moléculaire

    49 kDa

    ID gène

    7450

    UniProt

    P04275
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