Molecular marking method as well as kit and primer for identifying purity of broccoli hybrid scarlet pimpernel variety
A technology of variety purity and molecular markers, applied in biochemical equipment and methods, microbiological determination/inspection, DNA/RNA fragments, etc., can solve the problems of not being intuitive enough, time-consuming and labor-intensive, etc., and achieve the effect of shortening the detection cycle and rapid identification
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[0034] In the following, the present invention will be further illustrated by the embodiment of SSR marker analysis based on PCR technology.
[0035] The experimental materials in this example are the commercial seeds of broccoli 'Hailu' and its parents, and 4 other broccoli varieties commonly used in production (excellent, Lvxiong 90, excellent cold resistance, magpie).
[0036] Methods: DNA was extracted from broccoli leaves, PCR was amplified using SSR molecular markers, the amplified products were subjected to gel electrophoresis, the results were counted and characteristic primers were screened.
[0037] 1. Genomic DNA Extraction from Broccoli
[0038] Genomic DNA of broccoli was extracted by conventional methods.
[0039] 2. Molecular marker analysis
[0040] The SSR reaction system is genomic DNA 20 ng, Mg 2+ 1.8 mM, dNTP 0.2 mM, primer 0.6 μM, 1X PCR buffer, Taq DNA polymerase 0.8 U, add sterile ultrapure water to 15 μL. The PCR amplification reaction was carried ou...
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Abstract
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