Product Name: 2 In 1 (cTnI/CK-MB) Reagent Kit (Quantitative)
Method: Lateral-Flow technology (Fluorescent Immunochromatographic
Product Models: 5 tests/box, 25 tests/box, 40 tests/box, 100 tests/box
CFDA Registration No.: 20152400173
Certification: CE, SGS ISO13485, ISO9001
Matching Equipment's: Solid Phase Fluorescence Immunoassay System (KOFA Brand).
Introduction: This reagent kit is base on fluorescent chromatographic technology, supporting the quantitative rapid test of cTnI/CK-MB level in the serum/plasma. The combined testing of cTnI/CK-MB is used to diagnose myocardial injury and infarction.
cTnI/CK-MB Technical Parameters:
Test Item | Sample | Reacting Time | Testing Time |
cTnI/CK-MB | Plasma/Serum/Whole Blood:75μL | 15min | 3S |
The advantages of 2 In 1 (cTnI/ CK-MB):
1. Advanced fluoroimmunoassay quantitative testing platform, make accurate and quantitative rapid test of cTnI/CK-MB level available
2. Low cost and rapid test, can get the quantitative and reliable results in 15 minutes, shorten the testing turnaround time.
3. The testing results of this cTnI/CK-MB kit have good correlation with that of Roche Diagnostics (compared with thousands of samples).
4. Simple operation and rapid test, can meet the need of various departments.
5. The combined testing of cTnI and CK-MB is more convenient, accurate and efficient than single testing items, making the patients well-treated in the shorter time.
Applicable Departments: Departments of cardiology, surgery, geriatrics, respiratory, pediatrics, obstetrics, emergency ward and ICU.
Contact: Donald Qian
Phone: +86 172 4949 3008
Tel: +86 172 4949 3008
Company: Fortune BioSciences
Add: Gaoxin Avenue, East Lake New Technology Development Zone, 430075 Wuhan, Hubei, P.R. China.