|
Alternative Names |
IL-1B; IL1-B; IL1-Beta; IL1F2; IL-1β; Interleukin-1 Family Member 2; Catabolin |
|
Sensitivity |
5.9 pg/mL |
|
Reactivity |
Rat |
|
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 |
Cytokine, Tumor Immunity, Infection Immunity |
|
Uniprot ID |
Q63264 |
Standard Curve
|
Concentration (pg/mL) |
OD |
Corrected OD |
|
1000.00 |
2.195 |
2.110 |
|
500.00 |
1.657 |
1.572 |
|
250.00 |
1.136 |
1.051 |
|
125.00 |
0.828 |
0.743 |
|
62.50 |
0.496 |
0.411 |
|
31.25 |
0.315 |
0.230 |
|
15.63 |
0.189 |
0.104 |
|
0.00 |
0.085 |
0.000 |
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 levels of recombinant IL1b and the recovery rates were calculated by comparing the measured value to the expected amount of IL1b in samples.
|
Matrix |
Recovery Range |
Average |
|
Serum (n=5) |
80-95% |
87% |
|
EDTA plasma(n=5) |
88-103% |
95% |
|
Heparin plasma (n=5) |
95-107% |
101% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IL1b and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected
|
Matrix |
1:2 |
1:4 |
1:8 |
1:16 |
|
Serum (n=5) |
88-97% |
91-105% |
87-98% |
95-105% |
|
EDTA plasma(n=5) |
84-99% |
83-101% |
86-99% |
93-101% |
|
Heparin plasma (n=5) |
89-105% |
87-98% |
92-100% |
88-104% |
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 Rat IL1b. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat IL1b. 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 Rat IL1b, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulfuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Rat IL1b in the samples is then determined by comparing the OD of the samples to the standard curve.
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