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Liquimax Creatinine (End Point)

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INTENDED USE: Photometric in vitro assay for the quantitative determination of creatinine in human serum, plasma and Urine.

PRODUCT FEATURES :
1. Both End Point & Fixed Time procedures.
2. Three Liquid Reagents for End Point. (10 minutes End Point assay).
3. Two Liquid Reagents for Fixed Time.(2 minutes Fixed Time assay)
4. Working Reagent stability- 15 days at Room Temperature.
5. With Lipid Clearing Factor (LCF).
6. Linearity 25 mg/dl.
7. Tailor made for tropical Conditions.
8. Incorporates Six Sigma methodologies throughout the manufacturing
processes where in the product under goes various stringent process
checks like Defining, Measuring, Analyzing, Improving and Controlling.
(DMAIC)
9. No significant interference was observed from Bilirubin up to 20 mg/dl
(Both conjugated and unconjugated Bilirubin) Hemoglobin up to 50
mg/dl,Lipemia as Triglycerides up to 2000 mg/dl, Ascorbic acid up to 50
mg/dl.
10. Can be used on colorimeters and Semi-auto Analyzers.

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Description

In muscle metabolism, creatinine
is synthesized endogeneously from creatine and creatine phosphate. Under
conditions of normal renal function, creatinine is excreted by glomerular
filtration. Creatinine determinations are performed for the diagnosis and
monitoring of acute and chronic renal disease as well as for the monitoring of
renal dialysis. Creatinine concentrations in urine can be used as reference
values for the excretion of certain analytes (albumin, α-amylase)

Vendor Info

Vendor Information

  • Store Name: Avecon Healthcare
  • Vendor: Avecon Healthcare
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