serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length:
3.5h
Research Area:
Signal transduction;Infection immunity;Immune molecule;
Uniprot ID:
P80511
Test principle:
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 S100A12. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human S100A12. 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 S100A12, 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 S100A12 in the samples is then determined by comparing the OD of the samples to the standard curve.
標(biāo)準(zhǔn)曲線
Concentration (pg/mL)
OD
Corrected OD
5000.00
2.103
1.985
2500.00
1.755
1.637
1250.00
1.223
1.105
625.00
0.847
0.729
312.50
0.525
0.407
156.25
0.303
0.185
78.13
0.248
0.130
0.00
0.118
0.000
精密度
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.
回收率
Matrices listed below were spiked with certain level of recombinant S100A12 and the recovery rates were calculated by comparing the measured value to the expected amount of S100A12 in samples.
Matrix
Recovery range
Average
serum(n=5)
82-95%
88%
EDTA plasma(n=5)
89-103%
96%
Heparin plasma(n=5)
78-93%
85%
線性
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of S100A12 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.