PHOSPHORUS
Determination of phosphorus level in plasma, serum and urine is used to monitor and as an aid to the diagnosis of parathyroid and kidney diseases or vitamin D imbalance.
Increased phosphorus levels may be associated with increased phosphate intake, cell lysis (leukemia), transcellular phosphate shift (acidosis). Decreased phosphorus levels may occur in refeeding syndrome, decreased net intestinal phosphate absorption, lowered phosphate threshold in the kidneys.
Specification
|
Method |
phosphomolybdate UV |
|
Specimen |
serum, plasma, urine |
|
On board stability |
up to 12 weeks (1) |
|
Calibration stability |
up to 12 weeks (1) |
|
Measurement range |
0.11-19.0 mg/dL (0.036-6.137 mmol/L) (1) |
|
Regulatory status |
CE IVD |
|
Storage temperature (2) |
2-8°C |
(1) These results apply to the ACCENT MC240 analyser. Results may vary when a different instrument is used.
(2) 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
Liquick Cor-Phosphorus 30
Liquick Cor-Phosphorus 120
OS-PHOSPHORUS
HC-PHOSPHORUSACCENT-200
ACCENT-300
A-400
A-800
Prestige 24i
Prestige 24i LQ PHOSPHORUS (24 positions reagent tray)
Prestige 24i LQ PHOSPHORUS (36 positions reagent tray)
Available reagents
A-800 PHOSPHORUS
ACCENT-200 PHOSPHORUS
ACCENT-300 PHOSPHORUS
HC-PHOSPHORUS
LIQUICK COR-PHOSPHORUS
OS-PHOSPHORUS
PRESTIGE 24i LQ PHOSPHORUS
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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