Liquid phase chip kit for detecting refractory epilepsy
A liquid phase chip and kit technology, applied in the field of medicine and biology, can solve the problems of lack of high-level research on diagnostic markers, and achieve rapid detection, high-throughput detection, and good stability
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Embodiment 1
[0027] Embodiment 1, the preparation of liquid phase chip
[0028] 1. Preparation of Coated Microspheres
[0029] (1) Take the microsphere suspension (magnetic microspheres, bio-rad), vortex and sonicate for about 20 seconds, take 250 μL (about 5×10 6 microspheres) in a clean centrifuge tube (USA, Axygen), marked with the microsphere model and protein name; then put it into a centrifuge, separate at 14000g for 4min at room temperature, and then suck off the supernatant;
[0030] (2) Add 100 μL ddH to the centrifuge tube 2 O, vortex and sonicate for about 20s in turn, then separate at 14000g for 4min at room temperature, and suck off the supernatant;
[0031] (3) Add 160 μL of NaH with a pH of 6.2 and a concentration of 0.1M to the centrifuge tube 2 PO 4 , vortex and sonicate for about 20s, then add 20 μL N-hydroxysulfosuccinimide (S-NHS), vortex to mix, then add 20 μL 1-ethyl-(3-dimethylaminopropyl) Carbodiimide hydrochloride (EDC), vortex and sonicate for about 20s in tu...
Embodiment 2
[0039] Embodiment 2. The kit is used to detect refractory epilepsy
[0040] 1. Detection method
[0041] (1) Take out all the reagents from the kit before use and let it cool to room temperature;
[0042] (2) Take out the hippocampus tissues of rhesus monkeys with epilepsy and healthy rhesus monkeys, place them on ice to melt, vortex and mix well, and dilute the hippocampus tissues 20 times in a 96-well plate;
[0043](3) Prepare TIMP-1, MMP2, MMP3, and MMP9 standard proteins, take 7 EP tubes and mark them with S1, S2, S3, S4, S5, S6, and S7 respectively, and perform 2-fold serial dilutions, each standard protein dilution Afterwards, vortex to mix and replace the pipette tip;
[0044] (4) Take a 96-well plate, turn on the plate washer--Prime--rinse(channel2)--Prime--place the plate--Run5: MAGX3;
[0045] (5) Take the prepared capture antibody-coated microspheres, vortex and mix for 20s, sonicate for 20s, add 2500 microspheres per well into 1% PBS, vortex and mix for 20s, so...
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