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ELK Biotechnology
SKU:ELK3096
Human HYOU1(Hypoxia Up Regulated 1) ELISA Kit
Human HYOU1(Hypoxia Up Regulated 1) ELISA Kit
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$458.00 USD
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Human HYOU1(Hypoxia Up Regulated 1) ELISA Kit
Overview
| Product name: | Human HYOU1(Hypoxia Up Regulated 1) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | ORP150; HSP12A; Grp170; Glucose-Regulated Protein 170; 150 kDa oxygen-regulated protein |
| Assay Type: | Sandwich |
| Sensitivity: | 0.061 ng/mL |
| Standard: | 10 ng/mL |
| Range: | 0.16-10 ng/mL |
| Sample Type: | Serum, plasma, tissue homogenates and other biological fluids |
| Assay Length: | 3.5h |
| Research Area: | Signal transduction; |
| 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 HYOU1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human HYOU1. 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 HYOU1, 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 HYOU1 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 | 2.266 | 2.184 |
| 5.00 | 1.613 | 1.531 |
| 2.50 | 1.088 | 1.006 |
| 1.25 | 0.834 | 0.752 |
| 0.63 | 0.421 | 0.339 |
| 0.32 | 0.297 | 0.215 |
| 0.16 | 0.208 | 0.126 |
| 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 HYOU1 and the recovery rates were calculated by comparing the measured value to the expected amount of HYOU1 in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 80-95% | 87% |
| EDTA plasma(n=5) | 88-103% | 95% |
| Heparin plasma(n=5) | 95-107% | 101% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of HYOU1 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) | 85-92% | 79-96% | 89-101% | 85-97% |
| EDTA plasma(n=5) | 83-96% | 86-95% | 90-102% | 81-93% |
| Heparin plasma(n=5) | 81-94% | 96-105% | 92-103% | 82-96% |
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