Method for quickly identifying pseudo-ginseng
A Panax notoginseng and fast technology, applied in the field of identification of Panax notoginseng with specific SNPs, can solve the problems of identification obstacles, difficulties in identification of Panax notoginseng and its related species, high price of Panax notoginseng medicinal materials, etc., to achieve wide applicability and accurate identification. Effect
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Embodiment 1 10
[0024] The identification method of embodiment 1 Panax notoginseng medical material raw material
[0025] 1) 24 samples of Panax notoginseng collected from different medicinal material stores and genuine localities (Yunnan), each took 20 mg of medicinal material, and ground them on a MM400 ball mill (Retsch, Germany), and used plants from Tiangen Biochemical Technology (Beijing) Co., Ltd. Genomic DNA kit to extract total DNA.
[0026] Table 1 Panax notoginseng sample information table
[0027]
[0028]
[0029] 2) PCR amplification
[0030] The primer sequence is ITS2F: ATGCGATACTTGGTGTGAAT; ITS3R: GACGCTTCTCCAGACTACAAT, synthesized by Sangon Bioengineering Co., Ltd. (Beijing). Primers were dissolved in sterile deionized and diluted to 2 μmol / μL.
[0031] 25μL reaction system: PCR Buffer (10×) 2.5μL, Mg 2+ 2 μL (25 mmol / L), 2 μL (2.5 mmol / L) of dNTPs mixture, 1.0 μL (2.5 μmol / L) of each primer, 1 μL (-about 30 ng) of template DNA, 1.0 U of Taq DNA polymerase, add st...
Embodiment 2 10
[0043] Identification of embodiment 2 notoginseng decoction pieces
[0044] It is basically the same as Example 1, except that notoginseng decoction pieces are used as samples, DNA is extracted and identified, and as a result, the above two SNP sites can also be specifically detected. And the sequence comparison found that the 140th position of the ITS2 intergenic region sequence (SEQ ID No.1) of the Sanqi decoction piece DNA is T, and the 207th position is T.
Embodiment 3 10
[0045] The identification of embodiment 3 Panax notoginseng powder
[0046] Basically the same as Example 1, the difference is that notoginseng powder is used as a sample, DNA is extracted and identified, and the results can also specifically detect the above two SNP sites, and the sequence comparison shows that the ITS2 of the notoginseng powder DNA The 140th position of the intergenic region sequence (SEQ ID No.1) is T, and the 207th position is T.
[0047] SEQ ID No.1 in the sequence listing of the present invention is the consensus sequence of P. notoginseng.
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