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ELK Biotechnology
SKU:ELK9254
Human ACA-IgM(Anti-Cardiolipin Antibody IgM) ELISA Kit
Human ACA-IgM(Anti-Cardiolipin Antibody IgM) ELISA Kit
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$458.00 USD
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Human ACA-IgM(Anti-Cardiolipin Antibody IgM) ELISA Kit
Overview
| Product name: | Human ACA-IgM(Anti-Cardiolipin Antibody IgM) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | ACA-IgM; Anti-Cardiolipin Antibody IgM |
| Assay Type: | Sandwich |
| Sensitivity: | 0.082 ng/mL |
| Standard: | 20 ng/mL |
| Detection Range: | 0.31-20 ng/mL |
| Sample Type: | serum, plasma 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 Human ACA-IgM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACA-IgM. 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 Human ACA-IgM, 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 Human ACA-IgM 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 |
|---|---|---|
| 20.00 | 2.258 | 2.157 |
| 10.00 | 1.673 | 1.572 |
| 5.00 | 1.182 | 1.081 |
| 2.50 | 0.928 | 0.827 |
| 1.25 | 0.655 | 0.554 |
| 0.63 | 0.369 | 0.268 |
| 0.32 | 0.252 | 0.151 |
| 0.00 | 0.101 | 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 ACA-IgM and the recovery rates were calculated by comparing the measured value to the expected amount of ACA-IgM in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 90-105% | 97% |
| EDTA plasma(n=5) | 87-95% | 91% |
| Heparin plasma(n=5) | 80-97% | 88% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ACA-IgM 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) | 93-103% | 81-96% | 86-93% | 82-95% |
| EDTA plasma(n=5) | 87-105% | 83-92% | 92-105% | 92-101% |
| Heparin plasma(n=5) | 81-99% | 94-106% | 83-97% | 88-96% |
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