High Sensitive CE Approved CK-MB Test Kit For Creatine Kinase Isoenzyme

This CK-MB Test Kit (Time-Resolved Fluorescence Immunochromatographic Assay) can detect Creatine kinase isoenzyme (abbreviated as CK-MB below) in human serum/plasma/whole blood in vitro.

In the identification of acute myocardial infarction, CK-MB is commonly employed as a diagnostic marker of myocardial damage (AMI). It is often used to identify myocardial infarction. Clinical investigations have demonstrated that upon myocardial damage, CK-MB release reaches the bloodstream, peaks within 1224 hours, and recovers to normal levels by 4872 hours. As a result, detecting CK-MB is very important in the diagnosis of AMI. This project's detection platform primarily consists of chemiluminescence technology, immunocompetency technology, colloidal gold technology, immunofluorescence technology, time-resolved fluorescence technology, and other similar technologies.

• CK-MB Test Kit (Time-Resolved Fluorescence Immunochromatographic Assay): Contains 20/50 reagent cards,1 IC card,1 instruction for use,20 /50 sample buffers.
• The reagent card consists of plastic casings and test strips. The strip consists of a sample pad, a marker pad (Coated with a mouse anti-human CK-MB monoclonal antibody nano-microsphere fluorescent probe (0.5%, 1:40 Dilution)), Detection of the membrane ( Coated with mouse anti-human CK-MB monoclonal antibodies (1.5 mg/mL) and gout against mouse IgG polyclonal antibody (1.0 mg/mL)), absorbent paper and polystyrene (PVC) plywood. The sample buffer was 290 µL per person, and the main components were phosphate (PBS) buffer of 0.5% calf serum albumin (BSA) and 0.05% preservative Proclin-300( 2-methyl-4-isothiazoline-3-one and 5-chloro-2-methyl-4-isothiazoline-3-one).
• ※Do not exchange different batch numbers