Lablisa® Human p-cresol ELISA Kit

Product Information

Lablisa® Human p-cresol ELISA Kit

Catalog No : LAB1817 | 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 p-cresol. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human p-cresol. 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 p-cresol, 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 p-cresol in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:Lablisa® Human p-cresol ELISA Kit
Reactivity:Human
Alternative Names:4-Hydroxytoluene; 4-Methylphenol; p-Cresol 98+ %; PARA-CRESOL; 4-cresol; para cresol
Assay Type:Sandwich
Sensitivity:4.8 pg/mL
Standard:1000 pg/mL
Detection Range:15.63-1000 pg/mL
Sample Type:serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:3.5h
Research Area:Neuro science;


Standard curve



Concentration (pg/mL)ODCorrected OD
1000.002.1312.048
500.001.6471.564
250.001.1741.091
125.000.7280.645
62.500.5180.435
31.250.2620.179
15.630.1750.092
0.000.0830.000


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

MatrixRecovery rangeAverage
serum(n=5)78-94%86%
EDTA plasma(n=5)90-103%96%
Heparin plasma(n=5)81-96%88%


Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of p-cresol 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)87-96%86-95%91-103%87-93%
EDTA plasma(n=5)97-105%88-95%96-102%83-97%
Heparin plasma(n=5)89-103%85-93%89-97%95-102%


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