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Factor VIII anticorps

Cet anticorps anti-Factor VIII Monoclonal Souris (Clone n-a) (ABIN614478) détecte spécifiquement Factor VIII dans IHC (p). L’anticorps est réactif avec des échantillons de Humain.
N° du produit ABIN614478
735,38 €
Plus frais de livraison 40,00 € et TVA
50 μg
Destination: France
Envoi sous 17 jours ouvrables

Aperçu rapide pour Factor VIII anticorps (ABIN614478)

Antigène

Voir toutes Factor VIII (F8) Anticorps
Factor VIII (F8) (Coagulation Factor VIII (F8))

Reactivité

  • 110
  • 61
  • 31
  • 18
  • 10
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 101
  • 21
  • 9
  • 2
  • 2
  • 1
Souris

Clonalité

  • 113
  • 23
Monoclonal

Conjugué

  • 64
  • 17
  • 14
  • 8
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
Cet anticorp Factor VIII est non-conjugé

Application

  • 58
  • 46
  • 39
  • 39
  • 31
  • 15
  • 13
  • 10
  • 10
  • 6
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

N-a
  • Specificité

    This antibody recognizes full-length Human Factor VIII (F8). Does not cross-react with von Willebrand factor.

    Purification

    Protein G chromatography

    Immunogène

    F8 antibody was raised against purified human Factor VIII.

    Isotype

    IgG1
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    0.73 mg/mL

    Buffer

    PBS, pH 7.4

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    -20 °C

    Stockage commentaire

    Store the antibody at -20 °C to -70 °C.
  • Antigène

    Factor VIII (F8) (Coagulation Factor VIII (F8))

    Sujet

    This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation, factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder.Synonyms: AHF, Antihemophilic factor, F8C, Procoagulant component

    ID gène

    2157

    NCBI Accession

    NP_000123

    UniProt

    P00451
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