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Factor VIII Antikörper

Der Maus Monoklonal anti-Factor VIII Antikörper (Klon n-a) (ABIN614478) detektiert spezifisch Factor VIII in IHC (p). Dieser Antikörper reagiert spezifisch mit Proben aus Human.
Produktnummer ABIN614478
735,38 €
Zzgl. Versandkosten 20,00 € und MwSt
50 μg
Lieferung nach: Deutschland
Lieferung in 16 Werktagen

Kurzübersicht für Factor VIII Antikörper (ABIN614478)

Target

Alle Factor VIII (F8) Antikörper anzeigen
Factor VIII (F8) (Coagulation Factor VIII (F8))

Reaktivität

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

Wirt

  • 101
  • 21
  • 9
  • 2
  • 2
  • 1
Maus

Klonalität

  • 113
  • 23
Monoklonal

Konjugat

  • 64
  • 17
  • 14
  • 8
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
Dieser Factor VIII Antikörper ist unkonjugiert

Applikation

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

Klon

N-a
  • Spezifität

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

    Aufreinigung

    Protein G chromatography

    Immunogen

    F8 antibody was raised against purified human Factor VIII.

    Isotyp

    IgG1
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    0.73 mg/mL

    Buffer

    PBS, pH 7.4

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

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

    Hintergrund

    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

    Gen-ID

    2157

    NCBI Accession

    NP_000123

    UniProt

    P00451
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