Identification method of PCR-restriction map for fritillary bulb and similar medicine material
A technology of restriction endonuclease and polymerase, used in biochemical equipment and methods, DNA preparation, microbial determination/inspection, etc., can solve the problem of distinguishing Fritillaria fritillary from its counterfeit products, and achieve a reliable identification method. , It is not easy to cultivate, and the effect of ensuring the quality of medicinal materials
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[0013] 1. DNA extraction: proceed as usual, and adjust the DNA concentration of the test sample to 0.2-0.5 μg / μl with deionized water;
[0014] 2. Polymerase chain reaction:
[0015] (1) For polymerase chain reaction, 30 μl is used as a reference, and the dosages of various items are as follows:
[0016] 10×PCR buffer 3μl
[0017] MgCl 2 (25mM) 2.4μl
[0018] dNTP (each 10mM) 0.6μl
[0019] Primer P1, P2 (30pmol / μl) each 0.5μl
[0020] 1~2 μl DNA template for test product
[0021] TaqDNA polymerase 1U (0.2μl)
[0022] Deionized water make up to 30μl
[0023] (2) PCR reaction conditions: the reaction is carried out on a PCR instrument, and the reaction conditions are:
[0024] Pre-denature at 95°C for 3 minutes, and then carry out 30 cycles according to the following conditions:
[0025] Denaturation at 95°C for 20-40 seconds
[0026] Refolding at 53°C for 20-40 seconds
[0027] Extend at 72°C for 20-40 seconds ...
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