Chinese traditional medicine armand clematis polyase polymerase chain reactionidentification primer, reagent kit and identification method
A kind of Chuanketong and polymerase technology, which is applied in the direction of material analysis, instruments, and analysis materials through electromagnetic means, can solve the problems of different identification methods, and achieve the effect of high reproducibility and strong stability
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Embodiment 1
[0045] The preparation of embodiment 1 kit of the present invention
[0046] a. Specific identification primers: upstream primer: 5′-TGCCCAGCCTGCACAAGA-3′, downstream primer: 5′-TGCCCAGCCTCAACAGTGT-3′, the primers were synthesized by an automatic DNA synthesizer; each 1.0 μl;
[0047] b. Positive control substance: 1.0 μl of Chuanketong DNA template;
[0048] c. 1 unit of TaqDNA polymerase, 10×PCR reaction buffer, MgCl 2 , dNTP;
[0049] D, DNA extraction reagent; (the reagent that the present invention adopts all adopts commercially available routine reagent)
[0050] Among them, 10×PCR reaction buffer 2.5μl, 25mM MgCl 2 2.0 μl, 2.5 mM dNTP 1.5 μl.
Embodiment 2
[0051] Embodiment 2 Preparation of kit of the present invention
[0052] a. Specific identification primers: upstream primer: 5′-TGCCCCAGCCTGCACAAGA-3′, downstream primer: 5′-TGCCCAGCCTCAACAGTGT-3′, the primers were synthesized by an automatic DNA synthesizer; each 0.5 μl;
[0053] b. Positive control substance: 1.0 μl of Chuanketong DNA template;
[0054] c. 1 unit of TaqDNA polymerase, 10×PCR reaction buffer, MgCl 2 , dNTP (commercially available);
[0055] d, DNA extraction reagent (commercially available);
[0056] Among them, 10×PCR reaction buffer 2μl, 25mM MgCl 2 1.5 μl, 2.5 mM dNTP 1.0 μl.
Embodiment 3
[0057] Embodiment 3 Preparation of kit of the present invention
[0058]a. Specific identification primers: upstream primer: 5′-TGCCCAGCCTGCACAAGA-3′, downstream primer: 5′-TGCCCAGCCTCAACAGTGT-3′, the primers were synthesized by an automatic DNA synthesizer; each 1.5 μl;
[0059] b. Positive control substance: 2.0 μl of Chuanketong DNA template;
[0060] c. 1 unit of TaqDNA polymerase, 10×PCR reaction buffer, MgCl 2 , dNTP (commercially available);
[0061] d, DNA extraction reagent (commercially available);
[0062] Among them, 10×PCR reaction buffer 3μl, 25mM MgCl 2 3.0 μl, 2.5 μl of 2.5 mM dNTP.
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