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ELK Biotechnology
SKU:ELK2400
Rat NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
Rat NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
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$458.00 USD
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Rat NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit
Overview
| Product name: | Rat NT-ProANP(N-Terminal Pro-Atrial Natriuretic Peptide) ELISA Kit |
| Reactivity: | Rat |
| Alternative Names: | NT-Pro-ANP; N-ANP |
| Assay Type: | Sandwich |
| Sensitivity: | 0.247 ng/mL |
| Standard: | 40 ng/mL |
| Range: | 0.63-40 ng/mL |
| Sample Type: | Serum, plasma, tissue homogenates 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 Rat NT-ProANP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat 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 Rat 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 Rat 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 |
|---|---|---|
| 40.00 | 1.990 | 1.904 |
| 20.00 | 1.506 | 1.420 |
| 10.00 | 1.035 | 0.949 |
| 5.00 | 0.682 | 0.596 |
| 2.50 | 0.529 | 0.443 |
| 1.25 | 0.239 | 0.153 |
| 0.63 | 0.208 | 0.122 |
| 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 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) | 82-95% | 88% |
| EDTA plasma(n=5) | 90-105% | 97% |
| Heparin plasma(n=5) | 87-99% | 93% |
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) | 85-92% | 82-96% | 87-98% | 93-101% |
| EDTA plasma(n=5) | 88-102% | 86-92% | 91-103% | 89-97% |
| Heparin plasma(n=5) | 85-94% | 92-101% | 87-96% | 82-90% |
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