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Human IgG isotype control (HRP)

IsoC IgG HRP F(ab')2 fragment
N° du produit ABIN930164
  • Antigène Tous les produits IgG
    IgG
    Fragment
    F(ab')2 fragment
    Hôte
    • 140
    • 138
    • 121
    • 89
    • 86
    • 69
    • 56
    • 56
    • 47
    • 44
    • 38
    • 37
    • 34
    • 33
    • 27
    • 21
    • 16
    • 15
    • 9
    • 9
    • 4
    • 2
    Human
    Conjugué
    HRP
    Application
    Isotype Control (IsoC)
    Attributs du produit
    Human IgG protein (Fab'2) (HRP) conjugate
    Source: Human serum
    Alternative Names: Immunoglobulin G protein (Human) (Fab'2) (HRP)
    Physical state: Clear, colorless liquid
    Purification
    Human IgG protein (Fab'2) (HRP) was purified by delipidation, salt fractionation and ion exchange chromatography followed by papain digestion and dialysis.
    Isotype
    IgG
  • Indications d'application
    Optimal working dilutions should be determined experimentally by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Concentration
    Lot specific
    Buffer
    Lyophilized from 0.01 M Na1O4, pH 7.4, with 0.11 NaCl, 10 mg/mL BSA. Immunoglobulin and protease free.
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 4 °C until reconstitution. Following reconstitution aliquot and freeze at -20 °C for long term storage.
  • Antigène
    IgG
    Abstract
    IgG Produits
    Classe de substances
    Antibody
    Sujet
    Immunoglobulin G (IgG) are antibody molecules. Each IgG is composed of four peptide chains - two heavy chains and two light chains. Each IgG has two antigen binding sites. Other Immunoglobulins may be described in terms of polymers with the IgG structure considered the monomer. 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. Treatment with pepsin produces an F(ab)'2 fragment.
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