Probe and primer for detecting single nucleotide polymorphism related to chronic periodontitis, and kit thereof
A single nucleotide polymorphism, chronic periodontitis technology, applied in the biological field, can solve the problem of blank susceptibility to chronic periodontitis
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Embodiment 1
[0130] The assembly of embodiment 1 kit
[0131] Kit preparation:
[0132] Step 1, substrate processing and sampling
[0133] Wash the slides with double distilled water, soak them overnight in lye, take them out, wash them three times with double distilled water, then soak them in HCl with a volume fraction of 1% for 30 minutes, and put them in a slide tank after cleaning. use. The cleaned glass slides were aminated with 2% 4-aminobutyltriethoxysilane aqueous solution by volume, and then subjected to isothiocyanation treatment with 1mmol / L benzene isothiocyanate aqueous solution, and blown with nitrogen. After drying, store at 4°C in the dark.
[0134] Chip Zip probes are randomly combined oligonucleotide fragments with a length of 24bp. These oligonucleotide sequences are compared with the target genome sequence using the BLAST function on the NCBI website. The least derived set (as Zip probe sequences).
[0135] Zip probe for rs2891168 wild type: 5'-GCAAGTCTACCTAATCTCTGA...
Embodiment 2
[0146] The detection of embodiment 2 kit
[0147] Step 1, sample preparation
[0148] Saliva samples of each case were prepared, and genomic DNA was extracted from oral exfoliated cells of saliva by conventional phenol-chloroform method.
[0149] Step 2, PCR amplification
[0150] Using the genomic DNA of each sample as a template, PCR amplification was carried out with the specific amplification primer pair of rs2891168 and the specific amplification primer pair of rs1800796 respectively.
[0151] PCR reaction components (15μl system): 20ng genomic DNA, 2×Taq PCR Master Mix, 0.4μM each primer, RNase-free water complement.
[0152] The reaction conditions of Touch-down PCR are: start at 94°C for 5min, denature at 94°C for 30s, anneal at 64°C for 30s (down 0.5°C per cycle), extend at 72°C for 1min, cycle 14 times; denature at 94°C for 30s, anneal at 57°C for 30s , extended at 72°C for 1 min, cycled 30 times, and extended at 72°C for 10 min.
[0153] After the reaction was c...
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