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ELK Biotechnology
SKU:ELK3603
Human BSDL(Lipase, Bile Salt Dependent) ELISA Kit
Human BSDL(Lipase, Bile Salt Dependent) ELISA Kit
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$458.00 USD
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Human BSDL(Lipase, Bile Salt Dependent) ELISA Kit
Overview
| Product name: | Human BSDL(Lipase, Bile Salt Dependent) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | CEL; FAP; BAL; BSSL; FAPP; LIPA; MODY8; Carboxyl Ester Lipase; Bile salt-stimulated lipase; Bucelipase; Cholesterol esterase; Pancreatic lysophospholipase; Sterol esterase |
| Assay Type: | Sandwich |
| Sensitivity: | 0.058 ng/mL |
| Standard: | 10 ng/mL |
| Detection Range: | 0.16-10 ng/mL |
| Sample Type: | tissue homogenates, cell lysates, cell culture supernates and other biological fluids |
| Assay Length: | 3.5h |
| Research Area: | Enzyme & Kinase;Metabolic pathway;Infection immunity;Hepatology; |
| 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 BSDL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human BSDL. 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 BSDL, 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 BSDL 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 | 1.972 | 1.904 |
| 5.00 | 1.612 | 1.544 |
| 2.50 | 1.231 | 1.163 |
| 1.25 | 0.895 | 0.827 |
| 0.63 | 0.547 | 0.479 |
| 0.32 | 0.315 | 0.247 |
| 0.16 | 0.223 | 0.155 |
| 0.00 | 0.068 | 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 BSDL and the recovery rates were calculated by comparing the measured value to the expected amount of BSDL in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 78-92% | 85% |
| EDTA plasma(n=5) | 80-95% | 87% |
| Heparin plasma(n=5) | 78-96% | 87% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of BSDL 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% | 95-106% | 83-98% | 93-105% |
| EDTA plasma(n=5) | 88-101% | 90-98% | 92-106% | 85-97% |
| Heparin plasma(n=5) | 91-104% | 82-96% | 88-101% | 90-99% |
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