Primer pair for identifying American ginseng and application of primer pair
A primer pair and American ginseng technology, applied in the field of molecular biology, can solve the problems of unfavorable application and promotion of rapid identification, cumbersome fluorescent staining methods, and long testing time
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Embodiment 1
[0041] Embodiment 1, the preparation and use method of the kit for identifying American ginseng
[0042] 1. Design and synthesis of primer pairs for identification of American ginseng
[0043] In this example, the general primer matK (3F: 5'-CGTACAGTACTTTTTGTGTTTACGAG-3'1R: 5'-ACCCAGTCCATCTGGAAATCTTGGTTC-3') was selected to amplify the samples of Panax ginseng, Panax notoginseng, Panax notoginseng, Pearl ginseng and Panax notoginseng , sequenced, and then homologously compared the obtained sequences, and designed a pair of specific primers F1 and F2 according to the variable region, as a specific primer pair for identifying American ginseng. The sequence is as follows:
[0044] Primer F1: 5'-GGAAAATGCGGGTTATGACAGA-3' (SEQ ID NO: 1);
[0045] Primer F2: 5'-TTATGAGATTTGACTATCCCTTTGCTT-3' (SEQ ID NO: 2).
[0046] 2. Assembly of kits for identification of American ginseng
[0047] After the primers F1 and F2 designed and synthesized in step 1 are packaged separately, they are ...
Embodiment 2
[0060] Embodiment 2, using the kit prepared in embodiment 1 to identify American ginseng
[0061] Samples to be tested: 6 samples of Chinese herbal medicines shown in Table 1, Panax ginseng, Panax notoginseng, Bamboo ginseng, Pearl ginseng, and Panax notoginseng.
[0062] 1. Extract genomic DNA from the sample to be tested
[0063] Select about 0.03 g of dry medicinal material without mildew, put it in a pulverizer, grind it, and pass it through a 40-mesh sieve. Transfer the powder to a 2.0 mL microcentrifuge tube, add 900 μL of sterilized CTAB extract (recipe: 2% (2g / 100ml) CTAB, 100mmol / L Tris-HCl pH=8.0, 20mmol / L EDTA, 1.4mol / L NaCl), 0.02g PVP 40000, 10μL β-mercaptoethanol, fully vortexed and mixed, 65 ℃ water bath for 1.5h-2h, during which, shake gently 2-3 times. After completion, take it out and cool to room temperature, add 900 μL of chloroform-isoamyl alcohol (volume ratio 24:1), shake and mix well, and centrifuge at 12000 g for 10 min. Take the supernatant, add a...
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