Specific marker primer pair and identification method for rapid identification of Camellia oleifera Cenruan 2
A technology for an improved camellia seed and an identification method, which is applied in the field of rapid identification of a specific marker primer pair and identification of an improved camellia seed Cenruan No. 2, and can solve the problems of poor repeatability, complex PCR amplification patterns, and low specificity.
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Embodiment 1
[0022] (1) Extraction of genomic DNA from leaves of Camellia oleifera Cenruan 2 and the control group
[0023] Take 0.3 g of the young leaves of the improved Camellia oleifera to be tested, add liquid nitrogen and grind them thoroughly, and use a new type of rapid plant genomic DNA extraction kit (DP320, TIANGEN, Tiangen Biochemical Technology Beijing Co., Ltd.) to extract the genomic DNA to obtain the improved Camellia oleifera Genomic DNA crude extract. The DNA crude extract was subjected to 1.5% agarose gel electrophoresis and a DNA / RNA UV spectrophotometer (Nanodrop Teehnologies, USA) to detect integrity, purity and concentration, and DNA samples with OD260 / OD280>1.8 were used for subsequent PCR amplification . DNA extracts were stored in a -20°C refrigerator for later use.
[0024] (2) The sequence of the molecular-specific marker primer pair of Camellia oleifera Cenruan 2 (synthesized by Shanghai Bioengineering Technology Co., Ltd.)
[0025] Upstream primer: 5'-ATCATG...
Embodiment 2
[0034] (1) Extraction of genomic DNA from leaves of Camellia oleifera Cenruan 2 and the control group
[0035] Take 0.3 g of the young leaves of the improved Camellia oleifera to be tested, add liquid nitrogen and grind them thoroughly, and use a new type of rapid plant genomic DNA extraction kit (DP320, TIANGEN, Tiangen Biochemical Technology Beijing Co., Ltd.) to extract the genomic DNA to obtain the improved Camellia oleifera Genomic DNA crude extract. The DNA crude extract was subjected to 1.5% agarose gel electrophoresis and a DNA / RNA UV spectrophotometer (Nanodrop Teehnologies, USA) to detect integrity, purity and concentration, and DNA samples with OD260 / OD280>1.8 were used for subsequent PCR amplification . DNA extracts were stored in a -20°C refrigerator for later use.
[0036] (2) The sequence of the molecular-specific marker primer pair of Camellia oleifera Cenruan 2 (synthesized by Shanghai Bioengineering Technology Co., Ltd.)
[0037] Upstream primer: 5'-ATCATG...
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