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Description
Human IL-4 Kit (HICA)Product Specification Stability & Storage Store at 2~8C protected from light for 12 months; after reconstitution, the standard can be aliquoted and stored at 20C, avoiding repeated freeze thaw cycles. Background Principle of the Assay: This kit employs a homogeneous immuno chemiluminescence assay (HICA) based on the double antibody sandwich method for the detection of cytokine concentrations. The operation is simple and requires no washing steps. The
Product Specification
| Stability & Storage | Store at 2~8°C protected from light for 12 months; after reconstitution, the standard can be aliquoted and stored at -20°C, avoiding repeated freeze-thaw cycles. |
Background
Principle of the Assay:
This kit employs a homogeneous immuno chemiluminescence assay (HICA) based on the double-antibody sandwich method for the detection of cytokine concentrations. The operation is simple and requires no washing steps.
The detection system consists of two types of microspheres: receptor microspheres conjugated with antibody 1 targeting the protein of interest, and donor microspheres conjugated with streptavidin, along with biotin-labeled antibody 2. During the reaction, the target protein binds with the antibodies and microspheres to form an immune complex, bringing the two types of microspheres into close proximity. When the distance between the donor and receptor microspheres is less than 200 nm, singlet oxygen generated by light excitation can transfer to the receptor microspheres and trigger chemiluminescence. Conversely, if the target protein is absent, the distance between the microspheres remains too large, resulting in no signal.
By measuring the intensity of the chemiluminescent signal, quantitative analysis of the target protein can be achieved. This method is characterized by its simplicity, rapid reaction, and high sensitivity.
Components
Name |
Specification |
Component Specification |
Detection ReagentR1 |
500T |
2mL/Vial×1 |
2000T |
8ml/Vial×1 |
|
10000T |
40ml/Vial×1 |
|
Detection ReagentR2 |
500T |
2mL/Vial×1 |
2000T |
8ml/Vial×1 |
|
10000T |
40ml/Vial×1 |
|
Detection ReagentR3 |
500T |
5mL/Vial×1 |
2000T |
20ml/Vial×1 |
|
10000T |
100ml/Vial×1 |
|
Standard |
500T |
0.05μg Lyophilized Powder×1 |
2000T |
0.05μg Lyophilized Powder×2 |
|
10000T |
0.05μg Lyophilized Powder×5 |
|
Standard Buffer |
500T |
6mL/Vial×1 |
2000T |
12ml/Vial×1 |
|
10000T |
30ml/Vial×1 |
Note: Recommended plates for use are microplates (384 or 96-well plates, white, shallow wells)
Guidelines
Reagent R3 should be protected from light during use. Sample addition and incubation are recommended to be performed under green light (<100 LUX).
Recalibration is required for each test. Each concentration point of the standard should be tested in at least duplicate, and a four-parameter (weight 1/Y²) fitting calculation should be applied.
Temperature and time should be strictly controlled during incubation. The microplate should be covered with a film, and a microplate reader with ALPHA function is recommended.
The dilution matrix of the calibrator should be consistent with the test sample. It should be used within 2 hours after reconstitution.
Components from different reagent kit batches must not be mixed.
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