The HTRF human IL2 kit is designed for the quantification of human IL2 release in cell supernatant.
Feature | Specification |
---|---|
Application | Protein Quantification |
Sample Volume | 16 µL |
The HTRF human IL2 kit is designed for the quantification of human IL2 release in cell supernatant.
IL2's major role is to modulate cell-mediated immunity through its effect on T cells. IL2 promotes differentiation of T cells into effector or memory T cells, thus helping body fight off infection. IL2 is also a key player in immuno-oncology since it is main promoter of differentiation of T cells into Treg (regulatory T cells).
Assessment of serum samples often requires enhanced sensitivity. In some cases, AlphaLISA assays may have sufficient sensitivity to enable detection of low levels of analytes in serum or plasma.
Application |
Protein Quantification
|
---|---|
Brand |
HTRF
|
Detection Modality |
HTRF
|
Product Group |
Kit
|
Sample Volume |
16 µL
|
Shipping Conditions |
Shipped in Dry Ice
|
Target Class |
Cytokines
|
Target Species |
Human
|
Technology |
TR-FRET
|
Therapeutic Area |
Neuroscience
Oncology & Inflammation
|
Unit Size |
96 Assay Points
|
Cell supernatant, sample, or standard is dispensed directly into the assay plate for the detection by HTRF® reagents (384-well low-volume white plate or Cisbio low-volume 96-well plate in 20 µl). The antibodies labeled with the HTRF donor and acceptor are pre-mixed and added in a single dispensing step, to further streamline the assay procedure. The assay can be run up to a 1536-well format by simply resizing each addition volume proportionally.
The 4 Parameter Logistic (4PL) curve is commonly recommended for fitting an ELISA standard curve. This regression enables the accurate measurement of an unknown sample across a wider range of concentrations than linear analysis, making it ideally suited to the analysis of biological systems like cytokine releases.
Sample size | 16 µL |
---|---|
Final assay volume | 20 µL |
Kit components | Lyophilized standard, frozen detection antibodies, buffers &protocol. |
LOD &LOQ (in Diluent) | 7 pg/mL &37 pg/mL |
Range | 37 8,000 pg/mL |
Time to result | 3h at RT |
Calibration | NIBSC (86/500) value (IU/mL) = 0,01 x HTRF hIL2 value (pg/mL) |
Species | Human only |
Intra-assay (n=24)
Sample | Mean [IL2] (pg/mL) | CV |
---|---|---|
1 | 75 | 7% |
2 | 2997 | 3% |
3 | 6136 | 2% |
Mean CV | 4% |
Each of the 3 samples was measured 24 times, and % CV was calculated for each sample.
Inter-assay (n=4)
Sample | [IL2] (pg/mL) | Mean (delta R) | CV |
---|---|---|---|
1 | 98 | 346 | 12% |
2 | 432 | 1576 | 12% |
3 | 1904 | 5911 | 10% |
Mean CV | 11% |
Each of the samples was measured in 4 different experiments, and % CV was calculated for each sample.
Jurkat cells plated at 50 and 100 kcells/well were stimulated for 24 h with anti CD3 & and anti CD28 respectively prepared at 10 and 1 µg/mL. 16 µL of supernatants were transferred into a white detection plate (384 low volume) to be analyzed by the Human IL2 Assay.
Jurkat cells plated at 200 kcells/well were stimulated for 24 h with increasing concentrations of anti CD3 and anti-CD28: 0, 0.5, 1, 10 µg/mL for the anti CD3 and 0, 1, 5, 10, 20 µg/mL for the anti CD28. 16 µL of supernatants were then transferred into a white detection plate (384 low volume) to be analyzed by the Human IL2 Assay.
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