High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
- Product No.HEA710Hu
- Organism SpeciesHomo sapiens (Human) Same name, Different species.
- Test MethodDouble-antibody Sandwich
- Assay Length3h
- Detection Range0.11-80pg/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 0.04pg/mL.
- Sample TypeSerum, plasma and other biological fluids
- Download Instruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
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FOB
US$ 490
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Packages (Simulation)
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Packages (Simulation)
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Results demonstration
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Typical Standard Curve
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ISO9001: 2008, ISO13485: 2003 Registered
Specificity of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
This assay has high sensitivity and excellent specificity for detection of High Sensitive Prothrombin Fragment 1+2 (F1+2).
No significant cross-reactivity or interference between High Sensitive Prothrombin Fragment 1+2 (F1+2) and analogues was observed.
Recovery of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
Matrices listed below were spiked with certain level of recombinant High Sensitive Prothrombin Fragment 1+2 (F1+2) and the recovery rates were calculated by comparing the measured value to the expected amount of High Sensitive Prothrombin Fragment 1+2 (F1+2) in samples.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 81-99 | 95 |
| EDTA plasma(n=5) | 90-101 | 93 |
| heparin plasma(n=5) | 89-96 | 93 |
Precision of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level High Sensitive Prothrombin Fragment 1+2 (F1+2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level High Sensitive Prothrombin Fragment 1+2 (F1+2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of High Sensitive Prothrombin Fragment 1+2 (F1+2) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 87-103% | 91-105% | 83-90% | 93-105% |
| EDTA plasma(n=5) | 91-101% | 85-99% | 82-89% | 87-94% |
| heparin plasma(n=5) | 97-105% | 79-98% | 90-104% | 78-101% |
Stability of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Assay procedure summary of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
Test principle of the High Sensitive ELISA Kit for Prothrombin Fragment 1+2 (F1+2)
The microplate provided in this kit has been pre-coated with an antibody specific to F1. Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to F2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain F1+2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of F1+2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.