Special primer combination for quickly detecting polyploid of willow tree and detection method for polyploid
A detection method and primer combination technology, applied in biochemical equipment and methods, recombinant DNA technology, microbial determination/inspection, etc., can solve the problems of complex preparation process, increased difficulty, and the effect is not as good as that of animal cells, so as to improve detection The effect of high efficiency, high efficiency and simple operation
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Embodiment 1
[0025] The primers used in this method were developed from willow genome DNA sequence, and 192 pairs of primers were designed and developed by Primer Premier 5.0 software, and synthesized by Shanghai Jierui Biotechnology Co., Ltd.
[0026] Common willows are divided into arbor willows and shrub willows. In order to verify the versatility of the primers, this embodiment selected two common tree willows and two kinds of shrub willows, wherein the tree willows include weeping willow (Salix babylonica) and dry willow (S.matsudana), and the shrub willows include dustpan willow (S. suchowensis) and willow bark (S.integra). The collected cuttings were propagated by cuttings under greenhouse conditions, and the newly germinated young leaves were taken, and DNA was extracted by CTAB method. The concentration of the extracted DNA was detected with a micro-nucleic acid protein detector, and then the DNA concentration was diluted to 10 ng / μL, and stored at -20°C for later use. Each sele...
Embodiment 2
[0033] Weeping willow (Salix babylonica), dry willow (S.matsudana), dustpan willow (S.suchowensis) and willow willow (S.integra) preserved in the willow germplasm resources nursery of Nanjing Forestry University using the 10 pairs of primers screened in Example 1 A total of 48 samples of 4 species of willow were tested for genotype. The specific method is as follows:
[0034] The DNA of each sample was extracted from willow leaves according to the CTAB method. Afterwards, using this as a template, 10 pairs of primers obtained by screening were used for PCR amplification on an ABI-9700 thermal cycler. The total reaction system of PCR is 15 μL, which includes: template DNA 25ng, upstream and downstream primers 10ng each, concentration of 2.5mM dNTP 0.4μL, fluorescently labeled 1mM Fluorescein-12-dUTP (Roche Diagnostics) 0.01μL, Taq polymerase 0.5 U, 10×buffer (containing 100μM Tris-HCl pH 8.3, 500mM KCl, 20mM MgCl 2 and 10.0g / L BSA) 1.5 μL, add sterilized deionized water to s...
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