Specific primer pair and method thereof for identifying acorus calamus L. and acorus tatarinowii schott
A technique for Tibetan calamus and Shi calamus, which is applied in the field of identifying specific primer pairs of Tibetan calamus and Shi calamus respectively, can solve the problems of carcinogenicity, teratogenicity, confusion of names, etc., and achieve the effect of ensuring the quality of medicinal materials
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Embodiment 1
[0043] The method for identifying Tibetan calamus and Shichangpu includes the following steps:
[0044] 1. Extraction of medicinal DNA: proceed as usual, adjust the DNA concentration of the test sample to 0.2~0.5μg / μL with deionized water;
[0045] 2. Polymerase chain reaction:
[0046] (1) The polymerase chain reaction is based on 25μL, and the dosages of various items are:
[0047]
[0048]
[0049] (2) PCR reaction conditions: the reaction was performed on a PCR machine, and the reaction conditions were: 94°C pre-denaturation for 5 minutes, 94°C denaturation for 30s, 62°C annealing for 30s, 72°C extension for 45s, and after 35 cycles, 72°C extension for 10 minutes.
[0050] (3) Electrophoresis detection of PCR products: Take 5μL of the above reaction solution, mix it with 1.0μL loading buffer, and use 2% agarose gel (containing 0.5μg / μLGelRed) to detect the amplification results by electrophoresis. All DNA samples can be Amplify a DNA band of about 317bp;
[0051] 3. Restriction enzy...
Embodiment 2
[0059] In order to ensure the reliability of the molecular identification results, this experiment collected a variety of fake Tibetan calamus and Shichangpu and 50 common Chinese medicinal materials circulating in the market to verify the applicability of the experimental method to ensure that the method is accurate and reliable .
[0060] 1 Materials (see Table 1)
[0061] Table 1 Source of all samples of the present invention
[0062]
[0063]
[0064] 2DNA extraction
[0065] Take 0.1g of this product, wash with 1ml of 75% ethanol and 1ml of sterilized ultrapure water in turn, absorb the surface moisture, and grind it into a very fine powder in a mortar. Take 25mg, put it in a 1.5ml centrifuge tube, extract DNA with the new broad-spectrum plant genomic DNA rapid extraction kit, add 0.7mL 65℃ preheating buffer GP1, add mercaptoethanol to make the concentration 0.1%, mix gently, Place the centrifuge tube in a 65°C water bath for 20 minutes, shaking occasionally. Add 0.7 mL of chl...
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