Determination of factor X in plasma with Chromogenic Substrate S-2765™
The method is based on a two-stage principle. In stage one, Factor X is activated in the presence of calcium to Factor Xa (FXa) using the activator Russell’s Viper venom (RVV). In stage two, the generated FXa hydrolyses the chromogenic substrate Z-D-Arg-Gly-Arg-pNA (S-2765), thus liberating the chromophoric group pNA (p-nitroaniline). The color is then read photometrically at 405 nm. The generated FXa (and thus the intensity of color) is proportional to the FX activity of the sample.
Factor X → Factor Xa
Z-D-Arg-Gly-Arg-pNA + H2O → Z-D-Arg-Gly-Arg-OH + pNA
- S-2765, 25 mg Art. No. 82 14 13
Reconstitute the substrate S-2765 (MW: 714.6) with 20 ml sterile water.
- Russell’s Viper Venom (RVV)
Prepare a solution of Russell’s Viper Venom at a concentration of 0.087 mg/ml.
0.1 mol/l calcium chloride solution.
- Tris EDTA Buffer Art. No. 82 36 66
Dilute the buffer 1:10 with distilled water according to the insert sheet instructions.
- Normal Plasma
Calibrated, lyophilized or fresh frozen human plasma is used for the standardization of the assay. A pooled normal plasma can be prepared by taking samples from 20 healthy donors. 10-30 ml citrate blood (9 vol blood and 1 vol 0.1 mol/l sodium citrate) from each donor is centrifuged at 2000 x g for 20 minutes at 15-25°C. The plasma is pooled and subsequently dispensed in small volumes, which are frozen rapidly at -20°C or below. To avoid low temperature activation of prekallikrein the plasma is kept at 15-25°C before use or freezing. Thawing of plasma should be performed at 37°C and then kept at 15-25°C until used.
- RVV + CaCl2
Before use, mix 1 volume of RVV with 1 volume of CaCl2 . The mixture is stable for 48 hours at 2-8°C.
Acetic acid 20%
- Acetic acid is used as a stopper solution in the end-point method.
Blood (9 vol) is mixed with 0.1 mol/l sodium citrate (1 vol) and centrifuged at 2000 x g for 20 minutes at 20-25°C. Storage: 1 week at 2-8°C or 3-4 months at -20°C.
|FX%||Predilution – Normal plasma µl||Predilution – Buffer µl||Final dilution – Predil. plasma µl||Final dilution – Buffer µl|
|Test plasma or standard||50 µl|
|Acid stopped method||A||B|
|Diluted sample||200 µl||50 µl|
|Incubate at 37°C||3-4 min||3-4 min|
|Substrate (37°C)||200 µl||50 µl|
|Mix and add within 30 sec|
|RVV + CaCl2||200 µl||50 µl|
|Mix and incubate at 37°C||3 min||3 min|
|Acetic acid 20%||200 µl||50 µl|
A= test tube method
B= microplate method
Sample blank activities should be determined and subtracted when analyzing strongly colored plasma, e.g. lipemic and hemolytic. The sample blanks are prepared by mixing the diluted sample, acetic acid 20% and water instead of the reagents (400 µl for test tubes and 100 µl for microplates). Read the absorbance of the samples and blanks at 405 nm. The color is stable for at least four hours. When possible, use a dual wavelength mode with 490 nm as the reference wavelength.
Initial rate method:
When performing the initial rate method, transfer the microplate to a microplate reader immediately after the addition of RVV+CaCl 2 and read the change in A/min. The microplate reader must be pre-incubated at 37°C.
Plot A or ΔA/min for the standards against their concentration of Factor X. Read the Factor X value for the corresponding A or ΔA/min of the unknown test sample from the standard curve.
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