Molecular-specific marker primers for cherry blossom cultivars "Songyue" and "Yujin"
A labeled primer and specific technology, which is applied in the determination/inspection of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., can solve the difficulties in identification of phenotypic characteristics, application and promotion of garden plants, and difficulty in breeding new varieties and other problems, to achieve the effect of simple method
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[0038] (1) Extraction of Genomic DNA of Cherry Blossom Varieties:
[0039] Take 0.01g of the young leaves of the cherry blossom variety to be tested, add liquid nitrogen and grind them thoroughly, and use the SDS-CTAB method to extract the genomic DNA. After multiple extractions, the crude genomic DNA extract of the cherry blossom variety is obtained. The crude DNA was purified by Magabio Nucleic Acid Purification Kit (Bioer, Hangzhou, China), and detected by 1.5% agarose gel electrophoresis and DNA / RNA UV spectrophotometer (GeneQuant Pro, GE Healthcare). Integrity, Purity and Concentration. 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.
[0040] (2) Design specific PCR amplification primers, the sequence of the primer pair is:
[0041]The upstream primer: 5'-AGCGGCCGCACAAATTAAGAAAAA-3' and the downstream primer: 5'-AGCGGCCGCACTTTGAACGAT-3' were synthesized by Shanghai Bioengineeri...
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