Lablisa® Human TBA(Total Bile Acid) ELISA Kit

Product Information

Lablisa® Human TBA(Total Bile Acid) ELISA Kit

Catalog No : LAB9875 | 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 TBA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TBA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human TBA, biotin-conjugated antibody and enzyme-conjugated Avidin 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 TBA in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:

Lablisa® Human TBA(Total Bile Acid) ELISA Kit

Reactivity:

Human

Alternative Names:

TBA; Total Bile Acid

Assay Type:

Sandwich

Sensitivity:

0.91 ng/mL

Standard:

200 ng/mL

Detection Range:

3.13-200 ng/mL

Sample Type:

serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay Length:

3.5h

Research Area:

Hepatic function


Standard curve



Concentration (ng/mL)ODCorrected OD
200.001.9161.829
100.001.4971.410
50.001.1861.099
25.000.8720.785
12.500.5450.458
6.250.3610.274
3.130.1750.088
0.000.0870.000


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 TBA and the recovery rates were calculated by comparing the measured value to the expected amount of TBA in samples.

MatrixRecovery rangeAverage
serum(n=5)80-97%88%
EDTA plasma(n=5)96-109%102%
Heparin plasma(n=5)86-99%92%


Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of TBA 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)90-99%97-106%95-102%87-98%
EDTA plasma(n=5)93-105%82-101%91-103%95-102%
Heparin plasma(n=5)87-98%92-104%82-96%95-102%


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