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CD45.2 Antikörper (FITC)

Reaktivität: Maus FACS, IF Wirt: Maus Monoclonal Ks20-8 FITC
Produktnummer ABIN1112457
  • Target Alle CD45.2 Produkte
    CD45.2 (CD45 (CD45.2 Allogen))
    Reaktivität
    Maus
    Wirt
    • 54
    Maus
    Klonalität
    • 54
    Monoklonal
    Konjugat
    • 6
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser CD45.2 Antikörper ist konjugiert mit FITC
    Applikation
    • 50
    • 15
    • 7
    • 6
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Flow Cytometry (FACS), Immunofluorescence (IF)
    Produktmerkmale
    The 104 monoclonal antibody reacts with the mouse CD45 molecule, the leukocyte common antigen (LCA) in CD45.2-expressing mouse strains. The strains that express CD45.2 include the most commonly used mouse strains C57BL/6, BALB/c, C58, DBA/1, DBA/2, C3H/He, CBA, 129, A and AKR. CD45.2 is expressed by all leukocytes in these strains.
    Immunogen
    B10.S mouse thymocytes and splenocytes
    Klon
    Ks20-8
    Isotyp
    IgG2a
  • Applikationshinweise
    It is recommended for use in flow cytometry. Each lot of this CD45.2 antibody is quality control tested by immunofluorescent staining with flow cytometric analysis. For immunofluorescent staining, the suggested use of this reagent is less or equal to 0.25 µg per 10^6 cells in 100 µL volume. It is recommended that the reagent be titrated for optimal performance for each application.
    Kommentare

    Fluorescein isothiocyanate (FITC). Abs/Em: 494/ 519 nm.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Lagerung
    4 °C
  • Target
    CD45.2 (CD45 (CD45.2 Allogen))
    Andere Bezeichnung
    CD45.2 (CD45.2 Produkte)
    Hintergrund
    The 104 antibody does not react with mouse cells expressing the CD45.1 alloantigen. Additional reported applications (for the relevant formats) include: immunoprecipitation, in vivo and in vitro blocking of B cell responses, and immunohistochemical staining of acetone-fixed frozen sections.
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