Detection probe, liquid phase chip and detection method thereof for EGFR gene mutation sites
A liquid phase chip and detection method technology, applied in the field of molecular biology, can solve problems such as hindering the detection of mutant genes, and achieve the effects of avoiding interference, improving detection accuracy, and convenient sampling
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Embodiment 1
[0077] Preparation of liquid chip for EGFR gene mutation detection
[0078] 1. Probe sequence design and microsphere coating
[0079] For the wild-type and mutant sequences of exons 19 and 21 of the EGFR gene, specific oligonucleotide probes were designed. The 5'end of the probe is an amino group, followed by a 10 T spacer. The probe was synthesized by Shanghai Shenggong Biological Engineering Technology Service Co., Ltd. The probes are respectively coupled with different color-coded microspheres (purchased from Luminex) through covalent bonding (coating process). The probe sequence is shown in the following table:
[0080]
[0081]
[0082] The specific steps for coating each kind of microspheres are as follows:
[0083] (1) Centrifuge the dry probe powder at 10,000 rpm for 1 min;
[0084] (2) Use ddH 2 O dissolved to 0.1mM (0.1nmol / μl, about 70μl);
[0085] (3) Centrifuge for a short time to gather the solution at the bottom of the tube;
[0086] (4) Divide into 10μl and 2μl, ...
Embodiment 2
[0133] Using the liquid chip for EGFR gene mutation detection in Example 1 to detect non-small cell lung cancer serum samples
[0134] 1. Preparation of the sample to be tested (extraction of free nucleic acid from plasma, serum and pleural fluid):
[0135] Refer to the instructions of AxyPrep Whole Blood Genome Small Amount Extraction Kit, the detailed steps are as follows:
[0136] (1) Take about 2.5ml of the patient's anticoagulated venous blood or pleural effusion, centrifuge at 3000rpm for 15 minutes, take 300μl of supernatant and add it to a 1.5ml clean and sterile centrifuge tube;
[0137] (2) Add 500μl AP1 buffer to the centrifuge tube, vortex and shake to mix well;
[0138] (3) Add 100μl AP2 buffer and vortex to mix thoroughly;
[0139] (4) Centrifuge at 12,000 rpm for 10 minutes at room temperature;
[0140] (5) Carefully aspirate the supernatant and add it to the adsorption column AxyPrep on a 2ml collection tube, cover it, and centrifuge at 6,000rpm for 1 minute;
[01...
Embodiment 3
[0237] Using the liquid-phase chip for EGFR gene mutation detection in Example 1 to detect lung cancer tissue samples
[0238] Take the lung cancer tissue samples of patients 1-10 used in Example 2 for detection, and the specific process is as follows:
[0239] 1. Preparation of samples to be tested
[0240] Extraction of DNA from lung cancer tissue samples: Take 5-50 mg of tissue specimens after lung cancer surgery or biopsy, and after grinding, wash them with pH 7.4 PBS solution twice; the washed tissue specimens are resuspended in 1 ml of digestive juice (50 mmol / L Tris, 1mmo / LNa 2 EDTA, 0.5% Tween-20, 200ug / ml proteinase K 200, pH 8.5), digested in a water bath at 55°C for 1 hour, and inactivated proteinase K in a water bath at 99°C for 15 minutes; centrifuged at 12000 rpm for 10 minutes; take the supernatant and pass Phenol-chloroform-isoamyl alcohol extraction method, ethanol precipitation method to obtain DNA samples for PCR reaction. DNA can also be extracted by micro spi...
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