Nucleotide sequence, molecular probe and method for identifying taxus media seedling
A technology of Taxus mandia and nucleotide sequences, applied in biochemical equipment and methods, microbe measurement/inspection, DNA/RNA fragments, etc., can solve problems such as subjective discrimination bias and morphological differences, and achieve the method Simple, high-sensitivity, short-time results
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Embodiment 1
[0018] Example 1 : Preparation of characteristic nucleotide sequence of Taxus media
[0019] 1. Genomic DNA extraction
[0020] Cut 200 mg of the fresh leaves of Taxus chinensis seedlings and put them in a mortar, immediately add liquid nitrogen to grind to powder, and then use the UNIQ-10 column-type plant genome DNA extraction kit of Shanghai Shenggong Bioengineering Co., Ltd. to extract the yew plant genome For DNA, use 1% agarose gel for electrophoresis detection of the obtained DNA, and use an ultraviolet spectrophotometer to detect the DNA concentration, and dilute to 50ng / μl.
[0021] 2. SCoT-PCR reaction, electrophoresis detection
[0022] SCoT universal primer 3 (5’-CAACAATGGCTACCACCG-3’) was used for PCR amplification. The primers were synthesized by Shanghai Shenggong Bioengineering Co., Ltd. The reaction system was: 2μl 10×Buffer, 2μl MgCl 2 (25mM), 0.8μl dNTPs (10mM), 1μl SCoT primer 3 (10μM), 1μl template DNA (50ng / μl), 0.4μl Taq enzyme (2U / μl), 12.8μl ddH 2 O. The t...
Embodiment 2
[0027] Example 2: Preparation of MHSF / MHSR specific nucleotide probes for Taxus media, PCR amplification, and electrophoresis detection
[0028] On the basis of obtaining the specific nucleotide sequence of Taxus media, using Primer Primer 5.0 software to design the nucleotide sequence of MHSF / MHSR (respectively shown in SEQ ID NO.2 and SEQ ID NO.3) ), the primers were synthesized by Shanghai Shenggong Biological Engineering Co., Ltd. Then, the designed and synthesized primers MHSF / MHSR were used to perform amplification detection on different yew samples (see the description of the figure for details).
[0029] The PCR reaction system is 2μl 10×Buffer, 2μl MgCl 2 (25mM), 0.8μl dNTPs (10mM), 1μl primer MHSF (10μM), 1μl primer MHSR (10μM), 1μl template DNA (50ng / μl), 0.4μl Taq enzyme (2U / μl), 11.8μl ddH 2 O. The total volume is 20μl.
[0030] The PCR reaction program was 94°C pre-denaturation for 5 min; 35 cycles (94°C denaturation for 50 s, 58°C annealing for 50 s, 72°C extension...
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