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ELK Biotechnology
SKU:ELK9253
Human ACA-IgG(Anti-Cardiolipin Antibody IgG) ELISA Kit
Human ACA-IgG(Anti-Cardiolipin Antibody IgG) ELISA Kit
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$458.00 USD
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Human ACA-IgG(Anti-Cardiolipin Antibody IgG) ELISA Kit
Overview
| Product name: | Human ACA-IgG(Anti-Cardiolipin Antibody IgG) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | ACA-IgG; Anti-Cardiolipin Antibody IgG |
| Assay Type: | Sandwich |
| Sensitivity: | 1.032 ng/mL |
| Standard: | 200 ng/mL |
| Detection Range: | 3.13-200 ng/mL |
| Sample Type: | Serum, plasma, tissue homogenates 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-IgG. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACA-IgG. 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-IgG, 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-IgG 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 |
|---|---|---|
| 200.00 | 1.929 | 1.843 |
| 100.00 | 1.543 | 1.457 |
| 50.00 | 1.115 | 1.029 |
| 25.00 | 0.821 | 0.735 |
| 12.50 | 0.557 | 0.471 |
| 6.25 | 0.319 | 0.233 |
| 3.13 | 0.206 | 0.120 |
| 0.00 | 0.086 | 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-IgG and the recovery rates were calculated by comparing the measured value to the expected amount of ACA-IgG in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 80-95% | 87% |
| EDTA plasma(n=5) | 87-101% | 94% |
| Heparin plasma(n=5) | 89-103% | 96% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of ACA-IgG 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) | 93-101% | 79-96% | 92-105% | 91-99% |
| EDTA plasma(n=5) | 90-98% | 87-98% | 92-104% | 86-98% |
| Heparin plasma(n=5) | 81-98% | 78-90% | 91-99% | 97-103% |
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