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Glu HCY UA LDL-C - Rapid Reagent Kit for screening av kroniske sykdommer

Easy of operation, fully automatic,

Trenger ikke profesjonell drift/kalibrering


Oversikt

[e-postbeskyttet] The Glucose/Homocysteine/Uric Acid/Low Density Lipoprotein Cholesterol Reagent kit is intended to quantitatively determine the concentration of glucose (Glu), homocysteine (HCY), uric acid (UA) and low density lipoprotein cholesterol (LDL-C) in human serum. Clinically, it is mainly used for the monitoring of blood glucose level, auxiliary diagnosis of hyperhomocysteinemia, hyperuricemia, hypercholesteremia, coronary heart disease, atherosclerosis and the risk evaluation of cardiovascular diseases.


Tiltenkt bruk

The glucose concentration in serum reflects the status of glycemic control in real-time. Strict control of blood glucose level is essential in the prevention and treatment of blood glucose disorder such as diabetes.

Homocysteine is one of independent risk factors for the development of stroke, coronary arteriosclerosis and myocardial infarction, where high levels of homocysteine increases the risk of developing the diseases. Meanwhile, according to its metabolism feature, homocysteine concentration is also a sensitive indicator of vitamin B12 deficiency and folic acid deficiency.

UA is the end product of the metabolic breakdown of purines, and is filtered out of human body through kidney and in urine. In normal condition, the uric acid level in human body is in dynamic equilibrium. Elevated uric acid level is normally observed in patients with renal diseases. Thus, UA measurement is used as an aid in the diagnosis of early-stage renal injury.

Low density lipoprotein cholesterol can reflect the level of low density lipoprotein, which is also known as an atherogenic factor. Higher ratio of low density lipoprotein cholesterol among total cholesterol indicates increased risk of atherosclerosis. The precise measurement of low density lipoprotein cholesterol is significant in early prevention, diagnosis, treatment and curative effect of coronary heart disease, and is the main reference basis of prescription determination for hyperlipoproteinemia patients.


Produktegenskaper

Væskefasereaksjonssystem, ved bruk av enzymatisk metodikk fører til nøyaktig resultat

Resultat tilgjengelig om 12 minutter

Ferdigfylt patron og engangskassett

Enkel betjening, helautomatisk, ingen behov for profesjonell betjening/kalibrering



Spesifikasjon

Test Element

Glu/HCY/UA/LDL-C

Prøve

Serumblod

Reaksjonstid

12 minutter

Målingsrekkevidde

Glu: 1.0~30.0 mmol/L

HCY: 3.0~50.0 µmol/L

UA: 50~2500 µmol/L

LDL-C: 0.3~10 mmol/L

Kvalifisering

CE



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