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ADA Antikörper (AA 287-314)

Dieses Maus Monoklonal-Antikörper erkennt spezifisch ADA in WB und ELISA. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN3029872

Kurzübersicht für ADA Antikörper (AA 287-314) (ABIN3029872)

Target

Alle ADA Antikörper anzeigen
ADA (Adenosine Deaminase (ADA))

Reaktivität

  • 65
  • 35
  • 19
  • 14
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 76
  • 19
  • 1
Maus

Klonalität

  • 78
  • 18
Monoklonal

Konjugat

  • 52
  • 8
  • 6
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ADA Antikörper ist unkonjugiert

Applikation

  • 85
  • 41
  • 15
  • 15
  • 13
  • 13
  • 13
  • 12
  • 10
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA

Klon

608CT2-1-3
  • Bindungsspezifität

    • 15
    • 9
    • 8
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 287-314

    Aufreinigung

    Purified

    Immunogen

    A portion of amino acids 287-314 from the human protein was used as the immunogen for this ADA antibody.

    Isotyp

    IgG1
  • Applikationshinweise

    Titration of the ADA antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:100-1:250

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Aliquot the ADA antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    ADA (Adenosine Deaminase (ADA))

    Andere Bezeichnung

    ADA

    Hintergrund

    This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia.

    UniProt

    P00813

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling, Ribonucleoside Biosynthetic Process
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