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ELK Biotechnology
SKU:ELK9364
Human sHLA-G(soluble human leucocyte antigen G1) ELISA Kit
Human sHLA-G(soluble human leucocyte antigen G1) ELISA Kit
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$458.00 USD
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Human sHLA-G(soluble human leucocyte antigen G1) ELISA Kit
Overview
| Product name: | Human sHLA-G(soluble human leucocyte antigen G) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | sHLA-G |
| Assay Type: | Sandwich |
| Sensitivity: | 0.062 ng/mL |
| Standard: | 10 ng/mL |
| Detection Range: | 0.16-10 ng/mL |
| Sample Type: | serum, plasma, tissue homogenates and other biological fluids |
| Assay Length: | 3.5h |
| Research Area: | Apoptosis;Tumor immunity;Infection immunity;Immune molecule;Hematology;Reproductive science;Immunodeficiency;Autoimmunity; |
| 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 sHLA-G. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human sHLA-G. 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 sHLA-G, 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 sHLA-G 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 |
|---|---|---|
| 10.00 | 1.984 | 1.898 |
| 5.00 | 1.527 | 1.441 |
| 2.50 | 1.108 | 1.022 |
| 1.25 | 0.839 | 0.753 |
| 0.63 | 0.593 | 0.507 |
| 0.32 | 0.332 | 0.246 |
| 0.16 | 0.228 | 0.142 |
| 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 sHLA-G and the recovery rates were calculated by comparing the measured value to the expected amount of sHLA-G in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 81-95% | 88% |
| EDTA plasma(n=5) | 84-99% | 91% |
| Heparin plasma(n=5) | 87-99% | 93% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of sHLA-G 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) | 88-97% | 89-102% | 92-101% | 87-102% |
| EDTA plasma(n=5) | 84-98% | 91-98% | 83-101% | 87-98% |
| Heparin plasma(n=5) | 95-102% | 89-99% | 85-96% | 91-101% |
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