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Human IgM isotype control (HRP)

IsoC IgM HRP F(ab')2 fragment
Catalog No. ABIN930171
  • Target See all IgM products
    IgM
    Fragment
    F(ab')2 fragment
    Host
    • 54
    • 36
    • 34
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Conjugate
    HRP
    Application
    Isotype Control (IsoC)
    Characteristics
    Human IgM protein (Fab mu) (HRP) conjugate
    Source: Human serum
    Alternative Names: Immunoglobulin M protein (Human) (Fab mu) (HRP)
    Physical state: Clear, colorless liquid
    Purification
    Human IgM protein (Fab mu) (HRP) was purified by delipidation, salt fractionation and ion exchange chromatography followed by dialysis.
    Isotype
    IgM
  • Application Notes
    Optimal working dilutions should be determined experimentally by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    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.
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 4 °C until reconstitution. Following reconstitution aliquot and freeze at -20 °C for long term storage.
  • Target
    IgM
    Abstract
    IgM Products
    Synonyms
    IgM constant region Isotype Control, IGM Isotype Control
    Target Type
    Antibody
    Background
    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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