Pig Fibrinogen ELISA Kit is a Sandwich (quantitative) ELISA kit for the measurement of Pig Fibrinogen in Pig in Citrate plasma, EDTA Plasma, Heparin Plasma, Serum samples.
Application | Reactivity | Dilution info | Notes |
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Application sELISA | Reactivity Reacts | Dilution info - | Notes - |
Cleaved by the protease thrombin to yield monomers which, together with fibrinogen beta (FGB) and fibrinogen gamma (FGG), polymerize to form an insoluble fibrin matrix. Fibrin has a major function in hemostasis as one of the primary components of blood clots. In addition, functions during the early stages of wound repair to stabilize the lesion and guide cell migration during re-epithelialization. Was originally thought to be essential for platelet aggregation, based on in vitro studies using anticoagulated blood. However, subsequent studies have shown that it is not absolutely required for thrombus formation in vivo. Enhances expression of SELP in activated platelets via an ITGB3-dependent pathway. Maternal fibrinogen is essential for successful pregnancy. Fibrin deposition is also associated with infection, where it protects against IFNG-mediated hemorrhage. May also facilitate the immune response via both innate and T-cell mediated pathways.
Fibrinogen alpha chain, FGA
Pig Fibrinogen ELISA Kit is a Sandwich (quantitative) ELISA kit for the measurement of Pig Fibrinogen in Pig in Citrate plasma, EDTA Plasma, Heparin Plasma, Serum samples.
Sample | n | mean | SD | C.V. |
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Sample Serum | n 0 | mean - | SD - | C.V. < 10 |
Sample | n | mean | SD | C.V. |
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Sample Serum | n 0 | mean - | SD - | C.V. < 10 |
Fibrinogen in vitro ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the quantitative measurement of Fibrinogen protein in pig biological samples.
In this assay the Fibrinogen present in samples reacts with the anti-Fibrinogen antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, anti-FIB antibodies conjugated with horseradish peroxidase (HRP), are added. These enzyme-labeled antibodies form complexes with the previously bound FIB. Following another washing step, the enzyme bound to the immunosorbent is assayed by the addition of a chromogenic substrate, 3,3',5,5'-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of FIB in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of FIB in the test sample. The quantity of FIB in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.
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Representative standard curve using ab205090 Pig Fibrinogen ELISA Kit.
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