FKBP5 gene methylation detection primer and kit based on pyrosequencing technology
A technology of pyrosequencing and detection kit, which is applied in the direction of recombinant DNA technology, microbial measurement/inspection, biochemical equipment and methods, etc. It can solve the problems of easy misdiagnosis and missed diagnosis, complex clinical manifestations of systemic vasculitis, and lack of organization Pathological changes and other issues, to achieve the effect of strong pertinence, low cost, and convenient detection
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Embodiment 1
[0037] Example 1 Establishment of FKBP5 Gene Methylation Detection Kit Based on Pyrosequencing Technology
[0038] (1) The composition of the kit: it mainly includes the following components:
[0039] 1) FKBP5 gene-specific amplification primers FKBP5-F and FKBP5-R, the sequencing fragment to be amplified is the cg03546163 site of the FKBP5 gene; match.
[0040] The amplification primers and sequencing primers were designed according to the cg03546163 target site of the FKBP5 gene using PyroMark Assay Design 2.0 software (QIAGEN), and their sequences are as follows:
[0041] Amplification primers:
[0042] FKBP5-F: 5'-Biotin-TGAAATGTAATTTTATTGTATGTGGTTTAT-3' (the 5' end is labeled with biotin Biotin);
[0043] FKBP5-R: 5'-AAATAAATTAAACAATAATTCATCCTCAC-3'.
[0044] Sequencing primers:
[0045] FKBP5-S: 5'-TTAATTATTTATATAGAATAAGTTT-3'.
[0046] 2) Reagents for amplifying the target region of the FKBP5 gene (cg03546163 site) (Akry Biological Company, Code No. AG11104): Pro ...
Embodiment 2
[0052] Example 2 Application of FKBP5 Gene Methylation Detection Kit Based on Pyrosequencing Technology
[0053] (1) Blood cell DNA extraction (TIANamp Genomic DNA Kit, DP304)
[0054] 1) Take 200 μL of fresh or frozen human blood samples (provided by volunteers diagnosed with coronary heart disease from Guangdong Provincial People’s Hospital), and add buffer GA to make up for less than 200 μL.
[0055] 2) Add 20 μL Proteinase K solution and mix well.
[0056] 3) Add 200 μL buffer GB, mix thoroughly by inversion, place at 70°C for 10 minutes to make the solution clear, and briefly centrifuge to remove water droplets on the inner wall of the tube.
[0057] 4) Add 200 μL of absolute ethanol, shake and mix well for 15 seconds, at this time flocculent precipitation may appear, centrifuge briefly to remove water droplets on the inner wall of the tube cap.
[0058] 5) Add the solution and flocculent precipitate obtained in the previous step into an adsorption column, centrifuge at...
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