A colorectal cancer screening marker composition, its selection method, and colorectal cancer screening kit
A colorectal cancer and kit technology, applied in biochemical equipment and methods, recombinant DNA technology, microbial measurement/testing, etc., can solve the problems of unacceptable colonoscopy and low detection sensitivity of early lesions, and achieve improved inspection Sensitivity, increased acceptance, and reduced mortality effects
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[0086] 1. Take 5 mL of plasma and use Qiagen Plasma Free DNA Extraction Kit (Cat: 55204) to extract cfDNA.
[0087] 2. Take 20 ng of extracted cfDNA and HinP1I (Cat: R0124, NEB), HpaII (Cat: R0171, NEB), AciI (Cat: R0551, NEB), HpyCH4IV (Cat: R0619, NEB) four methylation sensitive Endonuclease (final concentration 10 U / μL), 20 μL system, incubate at 37°C for 16 h, inactivate the enzyme at 80°C for 20 min, the enzyme digestion system is shown in Table 3, cfDNA from leukocytes is cut.
[0088] Table 3 Methylation-sensitive endonuclease digestion system
[0089]
[0090] 3. Use all the incubated products as templates, add the above 6 pairs of target-specific primers (50 nM each) and 1 pair of internal reference primers (10 nM), and configure the system for multiplex PCR. The reaction system is shown in Table 4. Multiplex PCR The reaction program is: 98°C / 45 s; 8cycles (98°C / 15 s, 55°C / 30 s, 72°C / 30 s); 72°C / 1 min; 4°C / hold, multiple PCR products are obtained from the reaction...
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