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Fibrinogen antibody (FITC)

This Goat Polyclonal antibody specifically detects Fibrinogen in ELISA and IF. It exhibits reactivity toward Mouse.
Catalog No. ABIN458359

Quick Overview for Fibrinogen antibody (FITC) (ABIN458359)

Target

See all Fibrinogen Antibodies
Fibrinogen

Reactivity

  • 98
  • 39
  • 32
  • 27
  • 13
  • 8
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  • 1
  • 1
Mouse

Host

  • 86
  • 57
  • 39
  • 12
  • 2
  • 2
Goat

Clonality

  • 156
  • 41
Polyclonal

Conjugate

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  • 4
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  • 4
  • 2
  • 1
This Fibrinogen antibody is conjugated to FITC

Application

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  • 26
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  • 22
  • 20
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  • 13
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  • 1
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ELISA, Immunofluorescence (IF)
  • Specificity

    The antiserum does not cross-react with any other component of mouse 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

    Fluorescein isothiocyanate-conjugated IgG fraction of polyclonal goat antiserum to mouse 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. Hyperimmune antisera with strong precipitating activity are selected for fractionation by saltprecipitation and purification of the IgG fraction by DEAE-chromatography.

    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 mouse cells, tissues and body fluids in immuno-fluorescence, as detection reagent in non-isotopic methodology and solid phase immunochemistry (e.g. ELISA). 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 are usually between 1:20 and 1:80.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Concentration

    IgG protein concentration 10 mg/ml. Fluorescein/IgG protein molar ratio (F/P) approximately 1.9. No foreign proteins added.

    Buffer

    Fluorochrome-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 mouse 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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