Clinical Sensitivity, Specificity and Accuracy Sen sitvity and Specificity The Troponin l Rapid thst Device (Whole BLood/sem/plasma) has been evaluated with a leading commercial ctnl test using clinical specimens.the results show that the sensitivity of the troponin l rapid test device (whole blood/Serum/plasma) is 98.3% and the specificity is 98.8%,relatice to the contrast leading test
The Troponin I Rapid Test Device (Whole Blood/Serum/Plasma) is
a qualitative, membrane based immunoassay for the detection of
cTnI in whole blood, serum or plasma. The membrane is pre-
coated with capture reagent on the test line region of the
test. During testing,the whole blood, serum or plasma specimen
reacts with the particle coated with anti-cTnI antibodies. The
mixture migrates upward on the membrane chromatographically
by capillary action to react with capture reagent on the membrane
and generate a colored line. The presence of this colored line in th
e test line region indicates a positive result, while its absence
indicates a negative result. To serve as a procedural control,
a colored line will always appear in the control line region
indicating that proper volume of specimen has been added and
membrane wicking has occurred.
The Troponin I Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of human cardiac Troponin l in whole blood, serum or plasma as an aid in the diagnosis of mypcardial infarction (MI)
Hot Tags: cardiac marker series one step troponin i ctni whole blood serum plasma test cassette rapid diagnostic tool, China cardiac marker series one step troponin i ctni whole blood serum plasma test cassette rapid diagnostic tool manufacturers, suppliers
