CHOLINESTERASE
Determination of the level of cholinesterase activity (decrease) in serum or plasma is helpful in the diagnosis of liver diseases such as cirrhosis, chronic inflammation and cancer. The decrease in the enzyme activity is also observed in poisoning with organic phosphates, the use of oral contraceptives or congenital cholinesterase deficiency. The increase in enzyme activity occurs in the course of nephrotic syndrome, diabetes and triglyceridemia.
Specification
|
Method |
according to Deutsche Gesselschaft für Klinische Chemie (DGKC), colorimetric |
|
Specimen |
serum, plasma |
|
On board stability |
up to 12 weeks |
|
Calibration stability |
up to 12 weeks |
|
Measuring range |
38-21000 U/l |
|
Regulatory status |
CE IVD |
|
Storage temperature (1) |
2-8°C |
(1) For proper storage, follow the recommended temperature range available on the label. Full details are provided in the Instructions for Use/User Manual.
Transport and store at a controlled temperature in accordance with the product labeling. Deviations from the required conditions may affect the quality of the reagent.
Reagent lines
Multipurpose Line
CORMAY CHOLINESTERASE 30
CORMAY CHOLINESTERASE 60
OS-CHOLINESTERASE
HC-CHOLINESTERASEACCENT-200
ACCENT-300
A-400
Prestige 24i
Prestige 24i CHOLINESTERASE (24 positions reagent tray)
Prestige 24i CHOLINESTERASE (36 positions reagent tray)
Available reagents
ACCENT-200 CHOLINESTERASE
ACCENT-300 CHOLINESTERASE
CORMAY CHOLINESTERASE
HC-CHOLINESTERASE
OS-CHOLINESTERASE
PRESTIGE 24i CHOLINESTERASE
The specification was based on data determined on selected analyzers. We recommend that all users should refer to the instruction for use (IFU) and instruments’ user or service manuals before proceeding.
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