Lablisa® FastTrack Human cTnI(Cardiac Troponin I) ELISA Kit

Product Information

Lablisa® FastTrack Human cTnI(Cardiac Troponin I) ELISA Kit

Catalog No : LAB057FT | Pack Size : 48T , 96T

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human cTnI, and the Human cTnI standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human cTnI. After TMB substrate solution is added, only those wells that contain Human cTnI and HRP-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human cTnI in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:Lablisa® FastTrack Human cTnI(Cardiac Troponin I) ELISA Kit
Reactivity:Human
Alternative Names:TNNI3; TNNC1; CMH7; C-TnI; Troponin I Type 3; Cardiac troponin I; Troponin I
Assay Type:Sandwich
Sensitivity:19.6 pg/mL
Standard:25 ng/mL
Detection Range:0.39-25 ng/mL
Sample Type:Serum, plasma
Assay Length:1.5h
Research Area:Cardiovascular biology;

Standard curve



Concentration (ng/mL)ODCorrected OD
25.002.1032.008
12.501.5281.433
6.251.0880.993
3.130.8820.787
1.570.5090.414
0.790.3690.274
0.400.1700.075
0.000.0950.000


Precision

Intra-assay Precision (Precision within an assay):CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays):CV%<10%

Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.


Recovery

Matrices listed below were spiked with certain level of recombinant cTnI and the recovery rates were calculated by comparing the measured value to the expected amount of cTnI in samples.

MatrixRecovery rangeAverage
serum(n=5)78-95%86%
EDTA plasma(n=5)80-96%88%
Heparin plasma(n=5)80-92%86%


Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of cTnI and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Matrix1:21:41:81:16
serum(n=5)89-99%88-104%84-98%95-105%
EDTA plasma(n=5)95-104%87-96%92-101%82-90%
Heparin plasma(n=5)78-92%83-96%87-98%95-102%


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