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ELK Biotechnology
SKU(재고 관리 코드):ELK2401
Mouse NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
Mouse NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
Mouse NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
Overview
| Product name: | Mouse NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit |
| Reactivity: | Mouse |
| Alternative Names: | NT-Pro-ANP; N-ANP |
| Assay Type: | Sandwich |
| Sensitivity: | 29 pg/mL |
| Standard: | 5000 pg/mL |
| Range: | 78.13-5000 pg/mL |
| Sample Type: | Serum, plasma and other biological fluids. |
| Assay Length: | 3.5h |
| Research Area: | Endocrinology;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 Mouse NT-ProANP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse NT-ProANP. 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 Mouse NT-ProANP, 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 Mouse NT-ProANP 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 |
|---|---|---|
| 5000.00 | 1.983 | 1.894 |
| 2500.00 | 1.638 | 1.549 |
| 1250.00 | 1.088 | 0.999 |
| 625.00 | 0.728 | 0.639 |
| 312.50 | 0.589 | 0.500 |
| 156.25 | 0.239 | 0.150 |
| 78.13 | 0.168 | 0.079 |
| 0.00 | 0.089 | 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 NT-ProANP and the recovery rates were calculated by comparing the measured value to the expected amount of NT-ProANP in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 93-107% | 100% |
| EDTA plasma(n=5) | 87-99% | 93% |
| Heparin plasma(n=5) | 85-99% | 92% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of NT-ProANP 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) | 85-103% | 82-96% | 87-105% | 90-99% |
| EDTA plasma(n=5) | 88-102% | 86-92% | 81-93% | 79-87% |
| Heparin plasma(n=5) | 79-94% | 87-96% | 85-98% | 95-104% |
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