Protein chip kit for detecting inflammatory factors and preparation method thereof
A protein chip and inflammatory factor technology, applied in the field of biomedicine, can solve the problems of cumbersome operation, low sensitivity, expensive instruments, etc., and achieve the effect of overcoming cumbersome operation and less sample consumption.
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Embodiment 1
[0027] Example 1: Preparation of a protein chip kit for detecting inflammatory factors.
[0028]In order to detect whether there are corresponding inflammatory factors in the sample, the bottom membrane immobilized with specific antibodies against the following proteins: eotaxin (EOTAXIN), leukocyte inducer-2 (EOTAXIN-2), granulocyte Colony-stimulating factor, (GCSF), recombinant human granulomacrophage colony-stimulating factor (GM-CSF), intercellular adhesion molecule-1 (ICAM-1), interferon-γ (IFN-γ), activated human T cells A gene product (I-309), interleukin-1α (IL-1α), interleukin-1β (IL-1β), interleukin-2 (IL-2), interleukin-3 (IL -3), interleukin-4 (IL-4), interleukin-6 (IL-6), interleukin-6sR (IL-6sR), interleukin-7 (IL-7), interleukin IL-8 (IL-8), interleukin-10 (IL-10), interleukin-11 (IL-11), interleukin-12p40 (IL-12p40), interleukin-12p70 (IL- 12p70), interleukin-13 (IL-13), interleukin-15 (IL-15), interleukin-16 (IL-16), interleukin-17 (IL-17), chemokines Inter...
Embodiment 2
[0040] Example 2: The experiment of detecting inflammatory factors with the kit of the present invention.
[0041] The bottom film is placed in the matching square box. Since there are a plurality of chip lattices distributed on the bottom film of this embodiment, the square box is provided with 8 square grids in this embodiment. Each chip array is divided into mutually independent reaction areas. In this example, 8 square boxes are provided and made by RayBiotech. After adding 2 ml of blocking solution to each square, place it at room temperature and incubate for 30 minutes. Then perform the following steps in sequence:
[0042] 1. Add sample
[0043] Aspirate the blocking solution in each square, put 100 microliters to 5 ml of the sample diluted with the blocking solution into the square with a membrane, and then shake it on a shaker at room temperature for 1 to 2 hours, or in React at 4°C for 12-18 hours.
[0044] 2. Membrane washing
[0045] Washing solution I cleaning...
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