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| Product Name | High - Density Lipoprotein Cholesterol (HDL - C) Direct Assay Kit (Clearance Method) |
| Catalog No. | BLTR-0011 |
| Description | This High - Density Lipoprotein Cholesterol direct assay kit uses the clearance method for direct and specific quantitative detection of HDL - C in serum and plasma. It has excellent precision, low interference, and is helpful for researching HDL - C's role in cardiovascular protection |
| Test Target | High - Density Lipoprotein Cholesterol (HDL - C) |
| Methodology | Direct enzymatic (clearance method) |
| Measurement Range | 0.39-2.59 mmol/L |
| Sample Type | Serum, plasma |
| Assay Time | 10 min at 37°C |
| Wavelength | 600 nm |
| Linearity | 0.39-2.59 mmol/L |
| Precision (Intra-assay CV) | ≤2.5% |
| Precision (Inter-assay CV) | ≤3.5% |
| Stability (Unopened) | 18 months at 2-8°C |
| Stability (Opened) | 30 days at 2-8°C |
| Stability (Reconstituted) | 10 days at 2-8°C |
| Interference (Hemoglobin) | ≤500 mg/dL (no significant interference) |
| Interference (Bilirubin) | ≤20 mg/dL (no significant interference) |
| Interference (Lipemic) | ≤1000 mg/dL (no significant interference) |
| Reagent Composition | Clearance reagents, cholesterol oxidase, peroxidase, 4 - aminoantipyrine |
| Reagent Form | Liquid |
| Reagent Volume | R1: 32 mL×4; R2: 8 mL×4; Cal: 1 mL×1 |
| Calibration Type | External calibration |
| Calibration Levels | 4 levels |
| Incubation Temperature | 37°C |
| Detection Instrument | Clinical chemistry analyzer, UV - visible spectrophotometer |
| Application | Quantitative determination of HDL - C in serum/plasma to study its anti - atherosclerotic effects and lipid metabolism regulation |
| Cross - Reactivity | No cross - reactivity with LDL, VLDL |
| pH Range | 6.8-7.2 |
| Shelf Life | 18 months |
| Storage Condition | Store at 2-8°C |
For research use only, not for clinical use.
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