Fecal detection kit for advanced adenoid tumor and colorectal cancer related gene methylation locus
A detection kit and technology for colorectal cancer, applied in the medical field, can solve problems such as reduced sensitivity, difficulty in purchasing, and difficulty in large-scale use, and achieve high sensitivity and specificity, improved sensitivity, and low cost
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Embodiment 1
[0075] The present invention uses a nucleic acid extraction kit (product of Xiamen Aide Biomedical Technology Co., Ltd., article number: ADx-FF01 c1806264) to extract DNA from colorectal cancer tissue samples, advanced adenoma tissue samples, and paracancerous tissue samples. The extraction steps are as follows:
[0076] 1. According to the size of the tissue area of the FFPE section, scrape 1 to 5 pieces of FFPE samples into a 1.5mL centrifuge tube, add 1mL xylene, shake and mix for 10s;
[0077] 2. Centrifuge at 13000×g for 2 minutes at room temperature, carefully remove the supernatant (do not suck the precipitate);
[0078] 3. Add 1mL of absolute ethanol, shake and mix for 10s, centrifuge at 13000×g for 2min at room temperature, carefully remove the supernatant (do not suck the precipitate);
[0079] 4. Leave the lid open for 10 minutes at room temperature or 5 minutes at 37°C to allow the ethanol to fully evaporate.
[0080] 5. Add 180 μL Buffer DTL and 20 μL Proteina...
Embodiment 2
[0139] Primer probes were designed for the methylation regions of the four gene promoters of MAL / SDC2 / TFPI2 / Vimentin, and the primer probe positions were designed for the methylation hotspot regions described in Example 1, and the designed primer probe sequence SEQ ID NO. 1-131 as shown in Table 6:
[0140] Table 6 Primer probe information
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[0145] Use the nucleic acid extraction kit (product of Xiamen Aide Biomedical Technology Co., Ltd., product number: ADx-TI01c1814560) to extract DNA from the colorectal cancer cell line HCT15 / HCT116. The DNA extraction steps are as follows:
[0146] 1. Take 20-60mg of cell line samples and add 1mL of normal saline, shake and mix well, centrifuge at 1200g for 2min, carefully remove the supernatant;
[0147] 2. Add 180uL Buffer DTL, add 20uL Proteinase K Solution, vortex and mix, digest at 56°C until a relatively clear solution is obtained, which can be digested overnight;
[0148] 3. Take ou...
Embodiment 3
[0189] Compared directly using the QIAamp Fast DNA Stool Mini Kit (QIAGEN product, article number: 51604) to extract the stool sample DNA, then using the EpiTect Fast DNA Bisulfite Kit (QIAGEN company product, article number: 59826) to carry out bisulfite conversion, and the present invention in During the extraction process, two sample processing methods are completed: extraction, bisulfite conversion, washing purification and recovery. Quantus was used to detect the sample concentration, and the PCR reaction system was used to detect the sample recovery after different sample extraction and bisulfite conversion. Compare the advantages and disadvantages of each, and the specific operation steps are as follows.
[0190] Extract stool DNA first and then perform bisulfite conversion method: first use QIAamp Fast DNA StoolMini Kit (QIAGEN product, product number: 51604) to extract DNA from stool samples, and the extraction operation is as follows:
[0191] 1. Take 1g of feces sa...
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