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Fibrinogen antibody (Biotin)

This Goat Polyclonal antibody specifically detects Fibrinogen in ELISA, IHC and ICC. It exhibits reactivity toward Rat.
Catalog No. ABIN458659

Quick Overview for Fibrinogen antibody (Biotin) (ABIN458659)

Target

See all Fibrinogen Antibodies
Fibrinogen

Reactivity

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  • 1
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Rat

Host

  • 86
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  • 39
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Goat

Clonality

  • 156
  • 41
Polyclonal

Conjugate

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  • 2
  • 1
This Fibrinogen antibody is conjugated to Biotin

Application

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  • 1
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ELISA, Immunohistochemistry (IHC), Immunocytochemistry (ICC)
  • Specificity

    The antiserum does not cross-react with any other component of rat plasma. Inter-species cross-reactivity is a normal feature of antibodies to plasma proteins since they frequently share antigenic determinants. of this antiserum has not been tested in detail.

    Characteristics

    Biotin-conjugated IgG fraction of polyclonal goat antiserum to rat fibrinogen

    Purification

    Adsorption: Immunoaffinity adsorbed using insolubilized antigens as required, to eliminate antibodies cross-reacting with other with other plasma proteins. The use of insolubilized adsorption antigens prevents the presence of excess adsorbent protein or immune complexes in the antiserum. The IgG (7S) fraction is isolated and purified from the antiserum and contains the bulk of the defined antibody specificity. It is free of other serum proteins as tested by immunoelectrophoresis and double radial immunodiffusion.

    Immunogen

    Fibrinogen (clotting factor I) is a heat labile beta glycoprotein present in plasma. It is the precursor of fibrin, which is the key protein constituting the network of the blood clot. Thrombin converts fibrinogen to fibrin by limited proteolysis. Fibrin monomers polymerize to fibrin which is stabilized by cross-linking. Fibrinogen is isolated from fresh plasma after removing prothrombin. Freund’s complete adjuvant is used in the first step of the immunization procedure.

    Isotype

    IgG
  • Application Notes

    As reagent for the direct detection of fibrinogen in rat cells, tissues and body fluids in immunocytochemical and immunohistochemical assays, as detection reagent in non-isotopic methodology and solid phase immuno-chemistry (e.g. ELISA). As a second step an avidin or streptavidin conjugate of the user’s choice has to be used. 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 are between 1:500 and 1:3,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Concentration

    IgG protein concentration 10 mg/ml. Biotin/IgG protein molar ratio (B/P) approximately 6.6. No foreign proteins added.

    Buffer

    Biotin-coupled purified hyperimmune IgG lyophilized from a solution in phosphate buffered saline (PBS, pH 7.2)

    Preservative

    Without preservative

    Storage

    4 °C
  • Target

    Fibrinogen

    Background

    The reactivity of the antiserum is restricted to fibrinogen. In immunoelectrophoresis and radial immunodiffusion (Ouchterlony), using various antiserum concentrations against normal rat plasma a single precipitin line is obtained which shows a reaction of identity with the precipitin line obtained with purified fibrinogen. No reaction is obtained with any other plasma protein component or serum. However, the antiserum may also react with fibrin monomers, circulating fibrinopeptides and fibrin degradation products
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