Lipoprotein (a) Lp(a) reagent validated for use on the QuidelOrtho VITROS® 5600/XT 7600 Integrated System and VITROS® 4600 Chemistry System
Diazyme’s Lipoprotein (a) Lp(a) is a latex particle enhanced immunoturbidimetric assay for the in vitro quantitative determination of Lp(a) concentration in human serum or plasma (EDTA) and Lithium – Heparin plasma. The measurement of Lp(a) is useful in evaluating lipid metabolism disorders and assessing atherosclerotic cardiovascular diseases in specific populations, when used in conjunction with clinical evaluation.
Lipoprotein (a) Lp(a)
- The assay’s linear range extends up to 100 mg/dL
- Excellent Within-Run and Between-Run Precision with CV’s ≤ 3.7%
- Fast test results for a rapid turnaround time
- Reduce waste and operational expenses with the reagents extended on-board stability of up to two weeks (54 days)
- Formatted liquid reagents ready-to-use, requiring no preparation saving time and reducing sample handling errors
Now validated for use on QuidelOrtho VITROS® 5600/XT 7600 Integrated System and VITROS® 4600 Chemistry System
| Please order from QuidelOrtho at www.quidelortho.com | |||
Product | Catalog Number | Packaging | Method/Format |
Kit (276 Tests) | DZ131BKY1 | R1: 1 x 60 mL | Latex Enhanced |
Calibrator | DZ131BCal | 5 x 1 mL | Liquid Stable |
Control | DZ131BCon | 2 x 1 mL | Liquid Stable |
CLIA:
Ortho-Clinical Diagnostics VITROS 4600 Chemistry System {Diazyme Lipoprotein (a) Assay} – CLIA Document Number CR180078
Ortho-Clinical Diagnostics VITROS 5600 Chemistry System {Diazyme Lipoprotein (a) Assay} – CLIA Document Number CR180078
Ortho-Clinical Diagnostics VITROS XT 7600 Chemistry System {Diazyme Lipoprotein (a) Assay} – CLIA Document Number CR190268
For CLIA decision summary, please click here. Search with provided document number above.
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