Acid treatment agent, sample pretreatment method, kit and detection method for igf-i chemiluminescent immunoassay
A technology of chemiluminescent immunity and detection kits, which is applied in the direction of chemiluminescence/bioluminescence, biological testing, preparation of test samples, etc., which can solve the adverse effects of sample detection accuracy and repeatability, insufficient release of IGF-I, Unable to detect issues such as exact values
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Embodiment 1
[0069] A chemiluminescent immunoassay kit for IGF-I, comprising the following components:
[0070] 1) Acidic treatment agent: It is mainly composed of acetic acid solution with a concentration of 0.25mol / L and hydrochloric acid solution with a concentration of 0.05mol / L, according to the molar ratio of acetic acid and hydrochloric acid being 10:1. The value is 2.5.
[0071] 2) Magnetic microsphere system: magnetic microsphere solution coated with anti-IGF-I antibody 1, wherein: the concentration of anti-IGF-I antibody 1 is 50 μg / L, and the concentration of magnetic microspheres is 1.2 mg / ml.
[0072] 3) Marker system: ABEI-labeled anti-IGF I antibody 2 solution, wherein: the concentration of anti-IGF-I antibody 2 is 50 μg / L, and the concentration of ABEI is 0.5 mg / L.
[0073] 5) Calibrator solution: including a low-point calibrator solution with an IGF-I concentration of 63.218 ng / L and a high-point calibrator solution with an IGF-I concentration of 1124.680 ng / L.
[0074] 4...
Embodiment 2
[0086] A method for IGF-I chemiluminescent immunoassay using the detection kit of Example 1, which is basically the same as the detection method in Example 1, except that:
[0087] 1) Pretreatment: Add 10 μL of sample and 50 μL of acid treatment agent into the cuvette, mix well, and incubate at 37° C. for 5 minutes.
Embodiment 3
[0089] A method for IGF-I chemiluminescent immunoassay using the detection kit of Example 1, which is basically the same as the detection method in Example 1, except that:
[0090] 1) Pretreatment: Add 100 μL of sample and 50 μL of acid treatment agent into the cuvette, mix well, and incubate at 37° C. for 5 minutes.
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