Glu HCY UA LDL-C - ຊຸດກວດກາໂຣກເບົາຫວານ

ພາບລວມ

[email protected] 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.

ການນໍາໃຊ້ທີ່ຖືກຕ້ອງ

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.

ຄຸນນະສົມບັດຜະລິດຕະພັນ

ລະບົບປະຕິກິລິຍາໄລຍະຂອງແຫຼວ, ການນໍາໃຊ້ວິທີການ enzymatic ນໍາໄປສູ່ຜົນໄດ້ຮັບທີ່ຖືກຕ້ອງ

ຜົນໄດ້ຮັບທີ່ມີຢູ່ໃນ 12 ນາທີ

ຕື່ມຂໍ້ມູນໃສ່ກ່ອນ & ໄສ້ຕອງແບບໃຊ້ຄັ້ງດຽວ

ງ່າຍ​ຂອງ​ການ​ດໍາ​ເນີນ​ງານ​, ອັດ​ຕະ​ໂນ​ມັດ​ຢ່າງ​ເຕັມ​ທີ່​, ບໍ່​ຈໍາ​ເປັນ​ຕ້ອງ​ປະ​ຕິ​ບັດ​ງານ​ເປັນ​ມື​ອາ​ຊີບ / calibration​

ຂໍ້ມູນ