Composition for detecting colorectal cancer and kit and application thereof
A detection kit and technology for colorectal cancer, applied in the biological field, can solve problems such as limited diagnostic effect, only targeting a single gene, and unsatisfactory detection accuracy, achieving high accuracy, high sensitivity, early screening and The effect of diagnosis
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Embodiment 1
[0067] Example 1: Sample DNA Extraction and Bisulfite Conversion
[0068] 1. Sample processing and DNA extraction
[0069] The nucleic acid extraction kit of Guangzhou Dajian Biotechnology Co., Ltd. was used for extraction, and the operation was as follows:
[0070] 1) Preprocessing of samples to be tested:
[0071] (a) The pretreatment operation of the stool sample is as follows: take 15mL of fresh stool and put it into a 50mL centrifuge tube containing the stool preservation solution, place the 50ml stool preservation tube containing the sample in a rotary mixer and mix for 0.5 hours; Put the uniform sample in a centrifuge at 4200rpm for 30min, take the supernatant, and divide it into three 5mL cryopreservation tubes, each with 3mL; take a 1.5mL centrifuge tube, add 1mL of fecal cell suspension, 100μL of digestive solution LP , mix well and digest at 37°C for 20 minutes, centrifuge at 4000rpm for 10min, transfer the supernatant to a 2mL centrifuge tube for later use.
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Embodiment 2
[0094] Example 2: Screening of colorectal cancer tissue hypermethylation candidate genes and specific primers and probes
[0095] 1. Screening of candidate genes for fecal hypermethylation in patients with colorectal cancer
[0096] Through comprehensive analysis of literature research results, TCGA methylation chip database and transcriptome sequencing expression profiles, methylation sites with significant differences were screened, and through multiple data filtering analysis, SDC2, NPY, FGF5, and PDX1 were finally screened and determined as colorectal cancer cells. Candidate loci of hypermethylation in cancer.
[0097] 2. Screening of specific primers and probes for colorectal cancer methylation detection
[0098] 1) Design and screening of specific primers and probes
[0099] According to the nucleic acid sequences of SDC2, NPY, FGF5, and PDX1 mentioned above, the methylation primers and probes were designed on the Methyl primerExpress v1.0 software. After repeated desi...
Embodiment 3
[0114] Example 3: Clinical sample detection and verification kit effect
[0115] 1. Interpretation of colorectal cancer gene methylation detection kit results
[0116] 1) Threshold setting
[0117] It can be output automatically according to the instrument, or manually adjust the baseline according to the instruction of the instrument, set the threshold in the linear part of the logarithmic graph of the fluorescence value, export the data from the software and read the CT value.
[0118] 2) Judgment of the effectiveness of the kit
[0119] The internal reference gene of the negative quality control product is amplified and the CT value is ≤25, and the gene methylation detection site is not amplified; the internal reference gene and the gene methylation detection site of the positive quality control product are both amplified and the CT value is ≤25.
[0120] 3) Judgment of sample validity
[0121] a) If the internal reference gene is amplified and the CT value is ≤25, the a...
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