LAMP detection method of Arceuthobium sichuanense
A technique for spruce dwarf mistletoe, detection method, applied to spruce dwarf mistletoe. field, to achieve the effect of simple operation, simple operation and short detection cycle
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Embodiment 1
[0040] Example 1 Primer Design
[0041] According to the analysis of the nucleotide sequence information of the plastid gene clpP of the spruce dwarf mistletoe and its host spruce, select the specific region of the spruce dwarf mistletoe to design multiple pairs of LAMP-specific primers. The length of the primers is generally as follows. :
[0042] F3: 5'-CAAGGGGCTGATAGTGAA-3';
[0043] B3: 5'-GGATAAAAGATCCCATTGAGG-3';
[0044] FIP: 5'-TCCGCCAGGAGAGTTTATAAAAAAAGAATCAACTTATTAGTCTGATGGT-3';
[0045] BIP: 5'-GGTCATCCCAGGAGTCGCTACTAAAGCCTATACATATAGTCTGTAC-3'.
[0046] The above primers were synthesized by Beijing Sanbo Polygala Biotechnology Co., Ltd.
Embodiment 2
[0047] Example 2 extracts total DNA
[0048] 1. Take out 1.0-3.0g of the collected spruce dwarf mistletoe and healthy spruce from the ultra-low temperature refrigerator, immediately put them in a pre-cooled mortar, add liquid nitrogen to quickly grind them into powder;
[0049] 2. Use the plant genome extraction kit (Beijing Quanshijin Biotechnology Co., Ltd.) to extract the genomic DNA of the above samples, as follows:
[0050] 2-1. Add 250 μl RB1 solution and 15 μl RnaseA to two 2ml centrifuge tubes respectively, take 0.1 g of each of the above two ground powders, add them to the corresponding centrifuge tubes, and mix well;
[0051] 2-2. Place the centrifuge tube in a constant temperature water bath and incubate at 55°C for 15 minutes;
[0052] 2-3. Centrifuge the centrifuge tube, centrifuge at 4°C, 12000rpm for 5min, gently suck the supernatant into 4 clean centrifuge tubes to obtain the supernatant;
[0053] 2-4. Add 100μl solution PB1 to 2 supernatant centrifuge tubes ...
Embodiment 3
[0060] Example 3: Spruce Dwarf Mistletoe LAMP Amplification Reaction
[0061] The specific implementation steps of LAMP amplification are as follows:
[0062] 1) Add the following reagents to the PCR tube so that the total reaction volume is 25 μl:
[0063]
[0064] Among them, BstDNA polymerase is produced by New England Biotechnology (Beijing) Co., Ltd., dNTP
[0065] Produced for Beijing Quanshijin Biotechnology Co., Ltd.
[0066] 2) LAMP reaction conditions are as follows:
[0067] 60℃45min
[0068] 85℃10min
[0069] That is, mix well according to the above system, and incubate at 60°C for 45 minutes; at 85°C, 10min to inactivate the stDNA polymerase.
[0070] 3) LAMP result analysis
[0071] After the LAMP amplification system was reacted for 45 minutes, the reaction system was detected by 1% agarose gel electrophoresis, in which ddH 2 O is a blank control. Test results such as figure 1 As shown, those with expanded bands are positive, indicating that the samp...
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