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Chèvre anti-Rat IgA, IgG, IgM (Fc Region) Anticorps (HRP) - Preadsorbed

ELISA, IHC, ICC Polyclonal IgG HRP
N° du produit ABIN458688
  • Antigène Tous les produits IgA, IgG, IgM
    IgA, IgG, IgM
    Épitope
    • 74
    • 58
    • 30
    • 16
    • 9
    Fc Region
    Reactivité
    • 72
    • 47
    • 36
    • 27
    • 12
    • 6
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    Rat
    Hôte
    • 159
    • 55
    • 4
    • 3
    • 1
    Chèvre
    Clonalité
    • 218
    • 1
    Polyclonal
    Conjugué
    • 53
    • 39
    • 32
    • 27
    • 22
    • 11
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    HRP
    Application
    • 115
    • 110
    • 76
    • 73
    • 68
    • 55
    • 26
    • 24
    • 23
    • 22
    • 15
    • 15
    • 13
    • 12
    • 12
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC), Immunocytochemistry (ICC)
    Specificité
    The reactivity of the antiserum is directed to the Fc subunits of the major isotypes of the rat immunoglobulin system. No reaction is obtained with purified IgG/Fab or any non-Ig protein of rat serum, as tested by immunoelectrophoresis and double radial immunodiffusion. In immunoelectrophoresis and double radial immunodiffusion using various antiserum concentrations against normal rat plasma and serum, the characteristic IgG, IgA and IgM precipitin lines are obtained
    Attributs du produit
    Horseradish peroxidase-conjugated IgG fraction of polyclonal goat antiserum to rat IgG, IgA and IgM, Fc specific
    Peroxidase/IgG protein molar ratio (E/P) is approximately 1.7. Enzyme marker Horseradish peroxidase enriched for isoenzyme C (RZ=3.2).
    Purification
    Preadsorption: Immunoaffinity adsorbed using insolubilized Ig-depleted rat serum fractions and IgG/Fab as required to eliminate antibodies reacting with the common Fab portion of immunoglobulins or reacting with other serum proteins. The use of insolubilized adsorption antigens prevents the presence of excess adsorbent protein or immune complexes in the antiserum. Hyperimmune antisera with strong precipitating activity are selected for fractionation and purification of the IgG (7S) fraction containing the bulk of the defined antibody specificity. It is free of other serum proteins as tested by immunoelectrophoresis.
    Immunogène
    Purified polyclonal rat IgG, and homogenous IgA and IgM isolated from rat serum. Freund's complete adjuvant is used in the first step of the immunization procedure.
    Isotype
    IgG
  • Indications d'application
    In enzyme-immunocytochemical and immunohistochemical staining for the detection of cytoplasmic Ig at the cellular and subcellular level by staining of appropriately treated cell and tissue substrates, and to demonstrate circulating antibodies in serodiagnostic microbiology and autoimmune diseases. The absence of activity to the common Ig/Fab subunit prevents the reaction of this conjugate with immunoglobulins bounds to Fc receptors on non-lymphoid cells. This immunoconjugate is not pre-diluted.
    The optimum working dilution of each conjugate should be established by titration before being used. Excess labelled antibody must be avoided because it may cause high unspecific background staining and interfere with the specific signal. Working dilutions for histochemical and cytochemical use are usually between 1:50 and 1:250, in ELISA and comparable non-precipitating antibody-binding assays between 1:1,000 and 1:5,000.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    It is reconstituted by adding 1 mL sterile distilled water, spun down to remove insoluble particles, divided into small aliquots, frozen and stored at or below -24 °C.
    Concentration
    10 mg/mL
    Buffer
    Peroxidase-coupled purified hyperimmune goat IgG lyophilized from a solution in phosphate buffered saline (PBS, pH 7.2).
    Agent conservateur
    Without preservative
    Conseil sur la manipulation
    Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    Prior to use, an aliquot is thawed slowly in the dark at ambient temperature, spun down again and used to prepare working dilutions by adding sterile phosphate buffered saline (PBS, pH 7. 2). Repeated thawing and freezing should be avoided. Working dilutions should be stored at +4 °C, not refrozen, an d preferably used the same day. If a slight precipitation occurs upon storage, this should be removed by centrifugation. It will not affect the performance of the immunoconjugate.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    The lyophilized conjugate is shipped at ambient temperature and may be stored at +4 °C, prolonged storage at or below -24 °C.
  • Antigène
    IgA, IgG, IgM
    Autre désignation
    IgG + IgA + IgM (IgA, IgG, IgM Produits)
    Classe de substances
    Antibody
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