Probes, gene chip and kit for detecting folic acid gene polymorphism
A gene polymorphism and gene chip technology, which is applied in the determination/inspection of microorganisms, DNA/RNA fragments, recombinant DNA technology, etc., can solve the problem of large-scale deployment of expensive instruments in hospitals, complex nucleic acid extraction and purification steps, and long operating procedures. and other problems, to achieve the effect of reducing detection time and cost, high accuracy, fast and convenient accuracy
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Embodiment 1
[0065] A probe for detecting folic acid gene polymorphism, the sequence of the probe is:
[0066] MTHFR677-C probe: AAAAAAAAAACGTGATGATGAAATCGGCTC;
[0067] MTHFR677-T probe: AAAAAAAAAACGTGATGATGAAATCGACTC;
[0068] MTHFR1298-A probe: AAAAAAAAAACAAAGACACTTTTCTTCACTGGTC;
[0069] MTHFR1298-C probe: AAAAAAAAAAAAGACACTTGCTTCACTGGT;
[0070] MTRR66-A probe: AAAAAAAAAAACAGCTTGCTCACATATTTCTTC;
[0071] MTRR66-G probe: AAAAAAAAAAACACAGCTTGCTTGCTCACACA.
[0072] A gene chip containing the above-mentioned probes for detecting folic acid gene polymorphism, its preparation process comprises the following steps:
[0073] A silicon nitride film with a thickness of 47.5nm and a TSPS film of 13.5nm was coated on a silicon wafer (Si) with a thickness of about 2.5mm and a diameter of 20cm by a rotary vacuum coating machine and a vacuum vapor deposition method to prepare a corresponding biosensor , and covered with a 15nm polyphenylalanine-lysine coating, and finally treated with 10 μmol / L...
Embodiment 2
[0079] A kit for detecting folic acid gene polymorphism, comprising the gene chip in Example 1, PCR reaction system, hybridization buffer, washing solution, BW reaction solution and TMB chromogenic solution.
[0080] Wherein the composition of PCR reaction system is as shown in table 2:
[0081] Table 2: Composition of PCR reaction system
[0082]
[0083]
[0084] Wherein the sequence of the F-primer in the PCR reaction system is:
[0085] MTHFR677-F: 5'-TTGAGGCTGACCTGAAGCACTTGAAGGAG-3';
[0086] MTHFR1298-F: 5'-CTTTGGGGAGCTGAAGGACTA-3';
[0087] MTRR66-FP: 5'-CCTTGAAGTGATGAGGAGG-3'.
[0088] Wherein the sequence of the R-primer in the PCR reaction system is:
[0089] MTHFR677-R: 5'-CCTGGATGGGAAAGATCCCG-3';
[0090] MTHFR1298-R: 5'-CACTTTGTGACCATTCCGGTTT-3';
[0091] MTRR66-RP: 5'-CCACTGTAACGGCTCTAACC-3'.
[0092] The hybridization buffer includes 0.3 mol / L trisodium citrate, 3 mol / L sodium chloride, 0.3 mol / L sodium dodecyl sulfate and Triton X-100 0.1% aqueous ...
Embodiment 3
[0097] The gene chips and kits prepared in Example 1-2 were used for detection. The substance to be detected was a plasmid containing the target gene fragment. The above plasmids were all synthesized and provided by Shanghai Sangon Bioengineering Co., Ltd.
[0098] Wherein the target gene fragment includes one of the MTHFR677 (C / T) site, MTHFR1298 (A / C) site and MTRR66 (A / G) site, and the specific sequences of the target gene segment are as follows:
[0099] TTGAAGGAGAAGGTGTCTGCGGGAG[C / T]CGATTTCATCATCACGCAGCTTTTC;
[0100] TGGGGGGAGGAGCTGACCAGTGAAG[A / C]AAGTGTCTTTGAAGTCTTCGTTCTT;
[0101] AGGCAAAGGCCATCGCAGAAGAAAT[A / G]TGTGAGCAAGCTGTGGTACATGGAT.
[0102] The MTHFR677-C plasmid, the MTHFR1298-A plasmid and the MTRR66-A plasmid were mixed to obtain a mixed plasmid, and the mixed plasmid was dissolved in 1 mL of TE buffer so that the concentration of the plasmid was 2 μg / mL or 2000 ng / mL. Take 5 μL of the plasmid solution as the test substance and add it into the PCR reaction sys...
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