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Human IgM isotype control (HRP)

IsoC IgM HRP F(ab')2 fragment
Produktnummer ABIN930171
  • Target Alle IgM Produkte
    IgM
    Fragment
    F(ab')2 fragment
    Wirt
    • 61
    • 37
    • 36
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Konjugat
    HRP
    Applikation
    Isotype Control (IsoC)
    Produktmerkmale
    Human IgM protein (Fab mu) (HRP) conjugate
    Source: Human serum
    Alternative Names: Immunoglobulin M protein (Human) (Fab mu) (HRP)
    Physical state: Clear, colorless liquid
    Aufreinigung
    Human IgM protein (Fab mu) (HRP) was purified by delipidation, salt fractionation and ion exchange chromatography followed by dialysis.
    Isotyp
    IgM
  • Applikationshinweise
    Optimal working dilutions should be determined experimentally by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Konzentration
    Lot specific
    Buffer
    Lyophilized from 0.02 M K2 O4, pH 7.2, with 0.12 NaCl, 10 mg/mL BSA. Immunoglobulin and protease free.
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    Lagerung
    4 °C/-20 °C
    Informationen zur Lagerung
    Store at 4 °C until reconstitution. Following reconstitution aliquot and freeze at -20 °C for long term storage.
  • Target
    IgM
    Abstract
    IgM Produkte
    Synonyme
    IgM constant region Isotype Control, IGM Isotype Control
    Substanzklasse
    Antibody
    Hintergrund
    Immunoglobulin M, or IgM for short, is a basic antibody that is produced by B cells. It is the primary antibody against A and B antigens on red blood cells. IgM is by far the physically largest antibody in the human circulatory system. It is the first antibody to appear in response to initial exposure to antigen. The fragment antigen-binding (Fab fragment) is a region on an antibody that binds to antigens. It is composed of one constant and one variable domain of each of the heavy and the light chain. These domains shape the paratope - the antigen-binding site - at the amino terminal end of the monomer. The two variable domains bind the epitope on their specific antigens.
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