EGFR gene extron 20 mutational detecting probe, liquid phase chip and detecting method thereof
A technology of mutation detection and exon, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc. It can solve problems such as interference and hindrance to the detection of mutant genes, and achieve convenient sampling and simple steps , the effect of high sensitivity
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Embodiment 1
[0042] Example 1 Preparation of EGFR gene exon 20 mutation detection liquid chip kit
[0043] 1. Probe sequence design and microsphere coating
[0044] For the wild-type and mutant sequences of EGFR exon 20, design specific oligonucleotide probes, including base sequences of SEQ.ID NO: 1-6, for exon 20 wild-type probes, and SEQ.ID NO: 7-12, for exon 20 mutant probes, wherein, SEQ.ID NO: 4-6 is the reverse complementary sequence of SEQ.ID NO: 1-3, SEQ ID NO : 10-12 are the reverse complementary sequences of SEQ ID NO: 7-9, respectively.
[0045] The specific steps of each microsphere coating are as follows:
[0046] (1) Take the microsphere mother solution (purchased from Luminex Company) and vortex to form a microsphere suspension;
[0047] (2) Take out 8ul microsphere mother solution, containing 0.8×10 5 -1.2×10 5 microspheres into a 0.5ml centrifuge tube;
[0048] (3) Centrifuge at 10,000rpm for 3min, discard the supernatant;
[0049] (4) Add 10ul coupling solution (p...
Embodiment 2
[0062] Example 2 Detection of Lung Cancer Serum Samples Using EGFR Gene Mutation Detection Liquid Chip
[0063] 1. Preparation of samples to be tested (plasma, serum and pleural effusion supernatant free nucleic acid can be extracted according to the following methods):
[0064] Refer to the instructions of AxyPrep Whole Blood Genome Small Extraction Kit, the detailed steps are as follows:
[0065] (1) Take about 2.5ml of anticoagulated venous blood or pleural effusion from the patient, centrifuge at 3000rpm for 15 minutes, take 300μl of supernatant and add it to a 1.5ml clean and sterile centrifuge tube;
[0066] (2) Add 500 μl of AP1 buffer solution to the centrifuge tube, vortex and mix well;
[0067] (3) Add 100 μl of AP2 buffer, vortex and shake well;
[0068] (4) Centrifuge at 12,000 rpm for 10 minutes at room temperature
[0069] (5) Add the supernatant to the adsorption column AxyPrep placed on a 2ml collection tube, cover the lid, and centrifuge at 6,000rpm for 1 m...
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