Q-May Laboratory Coagulation Reagents
The correlation between FDP and D-dimer
P-FDP is the fibrin/fibrinogen degradation product. Fibrin clot that is generated in coagulation on the blood and fibrinogen are degradated by plasmin which is generated in fibrinolysis, generate fibrin/fibrinogen degradation product. The existence of FDP in the blood means the fibrinolysis has occurred in vivo.
D-dimer is the fibrin degradation product. Fibrin clot that is generated in coagulation on the blood is degradated by plasmin which is generated in fibrinolysis, generates fibrin degradation product (XDP). D-dimer is the general name of high molecular degradation product (mainly contain Y-Y/D-X-D fragment), medium molecular product (mainly contain D-Y/Y-D fragment) and low molecular product (mainly contain D-D/E fragment).
The existence of D-dimer in the blood means the fibrinolysis has occurred in vivo.
That is to say, it is useful to measure it as the diagnosis of DIC, various thrombotic diseases, and as the index of the treatment the follow-up.
Features
- Measured value is not reserved between FDP and D-dimer (in case of Factor Auto).
- The balance of primary fibrinolysis and the secondary fibrinolysis in the blood vessel can be perceived by measuring it together D-dimer and FDP.
- High molecular D-dimer, medium molecular one and low molecular one can be measured almost even.
- Factor Auto is available for various analytical instruments.
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Designation
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Packing
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Factor Auto D-dimer
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R1 Buffer: 11 mL x 2
R2 Latex Reagent: 6mL x 1
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D-dimer Calibrator
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1 mL x 5 kinds
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Factor Auto P-FDP
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R1 Buffer: 11 mL x 2
R2 Latex Reagent: 6mL x 1
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P-FDP Calibrator
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1 mL x 5 kinds
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Common diluent
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100 mL
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Multiple Sera N Control
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0.5 mL x 5
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Multiple Sera A Control
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0.5 mL x 5
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