It is suitable for breeding grapefruit co-dominant rfp molecular marker with red skin trait and its application
A molecular marker and co-dominant technology, which is applied in the determination/testing of microorganisms, biochemical equipment and methods, DNA/RNA fragments, etc., can solve the problems of single color, low efficiency, long breeding cycle, etc., and achieve high nutritional value , speed up the color and reduce the breeding workload
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Embodiment 1
[0039] 1. Preparation of genomic DNA of citrus such as pomelo, citron, lemon, and red summer orange
[0040] In this example, the improved CTAB method was used to extract the genomic DNA of citrus such as pomelo.
[0041] 2. Utilize the primer pair RFP F / R1 and RFP F / R2 developed by the applicant to amplify and analyze the genomic DNA of all the above-mentioned citrus such as pomelo, citron, lime, and red summer orange.
[0042] The PCR reaction system is as follows: 2μl PCR buffer, 2μl MgCl 2 , 0.4dNTPs, Taq DNA polymerase (both purchased from Takara Company), 100ng DNA, forward and reverse primers each 0.2μM, ddH 2 O supplemented to a final volume of 20ul. Thermal cycle parameters are: 95°C for 5min; 95°C for 30sec, 55°C for 45sec, 72°C for 45sec, 35 cycles; 72°C for 10min, 1 cycle; 4°C storage, the reaction is completed on the S1000 Thermal Cycler PCR instrument. The amplified product was detected by 1.0% agarose gel electrophoresis on a horizontal electrophoresis tank, ...
Embodiment 2
[0044] Example 2 Screening and Identification of the Hybrid Offspring of Red Pomelo and Guanxi Honey Pomelo
[0045] 1. Preparation of genomic DNA of about 200 strains of red skin pomelo, Guanxi honey pomelo and their hybrid offspring
[0046] In this example, the improved CTAB method was used to extract the genomic DNA of 200 strains of Red Pimelo, Guanxi Honey Pomelo and their hybrid offspring.
[0047] 2. Using the primer pair RFP F / R2 developed by the applicant to amplify and analyze the genomic DNA of red skin pomelo, Guanxi honey pomelo and their hybrid offspring
[0048] The PCR reaction system is as follows: 2μl PCR buffer, 2μl MgCl 2 , 0.4dNTPs, Taq DNA polymerase (both purchased from Takara Company), 100ng DNA, forward and reverse primers 0.2μM each, ddH2O supplemented to a final volume of 20μl. Thermal cycle parameters are: 95°C for 5min; 95°C for 30sec, 55°C for 45sec, 72°C for 45sec, 35 cycles; 72°C for 10min, 1 cycle; 4°C storage, the reaction is completed on t...
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