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CD59 Antikörper (full length)

Dieser Maus Monoklonal Antikörper detektiert spezifisch CD59 in IHC (p). Es zeigt Reaktivität gegenüber Proben von Human.
Produktnummer ABIN3025487
642,40 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für CD59 Antikörper (full length) (ABIN3025487)

Target

Alle CD59 Antikörper anzeigen
CD59

Reaktivität

  • 193
  • 17
  • 11
  • 11
  • 5
  • 4
  • 3
  • 1
  • 1
Human

Wirt

  • 112
  • 105
  • 7
  • 6
Maus

Klonalität

  • 141
  • 86
  • 1
Monoklonal

Konjugat

  • 105
  • 26
  • 17
  • 16
  • 9
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser CD59 Antikörper ist unkonjugiert

Applikation

  • 120
  • 97
  • 76
  • 59
  • 47
  • 40
  • 30
  • 29
  • 16
  • 14
  • 13
  • 13
  • 10
  • 9
  • 9
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Güteklasse

Carrier-free

Klon

MACIF-1193
  • Bindungsspezifität

    • 16
    • 13
    • 8
    • 6
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    full length

    Verwendungszweck

    CD59 Antibody (azide and preservative free)

    Keine Kreuzreaktivität

    Pavian, Pferd

    Produktmerkmale

    Reacts with human CD59, a 20 kDa glycosyl phosphatidyl-inositol (GPI)-anchored cell surface protein. CD59 regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. CD59 is widely distributed on cells in all tissues. It inhibits formation of MAC, thus protecting cells from complement-mediated lysis. The expression of CD59 on erythrocytes is important for their survival. Genetic defects in GPI-anchor attachment, that cause a reduction or loss of CD59 and CD55 on erythrocytes produce the symptoms of the disease paroxysmal hemoglobinuria (PNH). It is useful for study on GPI-anchored proteins, PNH and CD59 functions.

    Aufreinigung

    PEG precipitation

    Immunogen

    Recombinant full-length human protein was used as the immunogen for the CD59 antibody.

    Isotyp

    IgM, kappa
  • Applikationshinweise

    Optimal dilution of the CD59 antibody should be determined by the researcher.

    1. Staining of formalin-fixed tissues requires boiling tissue sections in 10 mM Citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 min.
    2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Konservierungsmittel

    Azide free

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store the CD59 antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • Target

    CD59

    Andere Bezeichnung

    CD59

    Hintergrund

    Reacts with human CD59, a 20 kDa glycosyl phosphatidyl-inositol (GPI)-anchored cell surface protein. CD59 regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. CD59 is widely distributed on cells in all tissues. It inhibits formation of MAC, thus protecting cells from complement-mediated lysis. The expression of CD59 on erythrocytes is important for their survival. Genetic defects in GPI-anchor attachment, that cause a reduction or loss of CD59 and CD55 on erythrocytes produce the symptoms of the disease paroxysmal hemoglobinuria (PNH). It is useful for study on GPI-anchored proteins, PNH and CD59 functions.

    UniProt

    P13987

    Pathways

    Komplementsystem
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