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ELK Biotechnology
SKU(재고 관리 코드):ELK9455
Horse cTnT/TNNT2(Troponin T Type 2, Cardiac) ELISA Kit
Horse cTnT/TNNT2(Troponin T Type 2, Cardiac) ELISA Kit
Horse cTnT/TNNT2(Troponin T Type 2, Cardiac) ELISA Kit
Overview
| Product name: | Horse cTnT/TNNT2(Troponin T Type 2, Cardiac) ELISA Kit |
| Reactivity: | Horse |
| Alternative Names: | CMH2; cTnT; TnTc; Cardiomyopathy,Hypertrophic 2; Cardiac muscle troponin T; TNNT2; Troponin T Type 2, Cardiac |
| Assay Type: | Sandwich |
| Sensitivity: | 6 pg/mL |
| Standard: | 1000 pg/mL |
| Detection Range: | 15.63-1000 pg/mL |
| Sample Type: | serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids |
| Assay Length: | 3.5h |
| Research Area: | Cardiovascular biology; |
| Test principle: | The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Horse cTnT/TNNT2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse cTnT/TNNT2. 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 Horse cTnT/TNNT2, 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 Horse cTnT/TNNT2 in the samples is then determined by comparing the OD of the samples to the standard curve. |
Standard curve
| Concentration (ng/mL) | OD | Corrected OD |
|---|---|---|
| 1000.00 | 2.179 | 2.097 |
| 500.00 | 1.612 | 1.530 |
| 250.00 | 1.273 | 1.191 |
| 125.00 | 0.897 | 0.815 |
| 62.50 | 0.567 | 0.485 |
| 31.25 | 0.369 | 0.287 |
| 15.63 | 0.206 | 0.124 |
| 0.00 | 0.082 | 0.000 |

Precision
Intra-assay Precision (Precision within an assay):CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-assay Precision (Precision between assays):CV%<10%
Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.
Recovery
Matrices listed below were spiked with certain level of recombinant cTnT/TNNT2 and the recovery rates were calculated by comparing the measured value to the expected amount of cTnT/TNNT2 in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 90-105% | 97% |
| EDTA plasma(n=5) | 82-97% | 89% |
| Heparin plasma(n=5) | 84-98% | 91% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of cTnT/TNNT2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
| Matrix | 1:2 | 1:4 | 1:8 | 1:16 |
|---|---|---|---|---|
| serum(n=5) | 90-101% | 92-102% | 81-93% | 86-98% |
| EDTA plasma(n=5) | 84-98% | 95-103% | 86-98% | 89-98% |
| Heparin plasma(n=5) | 95-103% | 86-93% | 91-96% | 87-98% |
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