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By certification 
Intended use
This device is intended to be used for the in vitro quantitative determination of total thyroxine (CRP) in human whole blood, peripheral blood, serum or plasma. And it is for professional use only, not for self-testing of untrained individuals, nor for near-patient testing.
Summary
C-reactive protein (CRP) is synthesized by hepatocytes. When the body is infected or tissue is damaged, macrophages and other leukocytes are activated to produce interleukin-6 (IL-6), interleukin-1 (IL-1), tumor necrosis factor TNF-a and other cytokines and other mediators, these cytokines and mediators reach the liver and stimulate hepatocytes and epithelial cells to synthesize C-reactive protein. Detection of C-reactive protein includes conventional C-reactive protein (conventional CRP) and high-sensitivity C-reactive protein (high-sensitivity CRP). The detection objects of the two are essentially the same, but the quantitative range of the detection methods is different. The concentration of conventional C-reactive protein can rapidly increase within a few hours of acute inflammation, and its increase is positively correlated with the degree of infection. It is a widely used as inflammatory marker and can be used to evaluate tissue damage and inflammatory diseases, and provide reference information for the diagnosis, treatment, and monitoring of disease. A common use of high-sensitivity C-reactive protein is as an aid in cardiovascular disease risk identification. Combined with the traditional clinical diagnosis of acute coronary syndrome, the high-sensitivity C-reactive protein result can be used as an early warning indicator of coronary artery disease or acute coronary syndrome recurrence. The detection range of full-range C-reactive protein (full-range CRP) covers the detection range of both conventional CRP and hypersensitive CRP.
Current clinical methods for detecting CRP include chemiluminescence method, immunochromatography method, and etc.
TEST INFORMATION | |||
Method |
Microfluidic Fluorescent Immunoassay |
Test |
LYOFIA® CRP |
Format |
Cassette |
Reaction Time |
5min |
Linearity |
0.4～100mg/L |
Reference Interval |
hs-CRP≤1mg/L |
Sample |
WB / S / P / FB |
Certificate |
CE/NMPA |
ORDERING | |||||
Cat. No. |
LMFMCR25 |
Applicable analyzer |
LYOFIA-I, LYOFIA 8, |
Kit Size |
25T |
Cat. No. |
LAFMCR25 |
Applicable analyzer |
LYOFIA 100 (Full-Automatic) |
Kit Size |
25T |
Hospitals
Laboratory
Clinics
Ambulance
Cardiology
Pediatrics
Emergency
CSC
Q: Is it possible to OEM?
A: Yes. Clients need to authorize brands and provide design solutions.
Q: How long is the usual delivery time?
A: The regular delivery time is about 2 weeks. If you need to do new packaging (OEM), the delivery time for the first order is 25-30 days, and the second order starts and the regular delivery time is the same.
Q: Are there any requirements for reagent storage? ,
A: The storage temperature of our reagents is room temperature, 2-30℃
Q: Reagent expiration date?
A: 12 months.
http://www.vacurebiotech.com/
