Molecular markers and methods for identifying a06 and c05 chromosome segregation in Brassica vegetable interspecific hybrids and progeny materials
A chromosome and Brassica technology, applied in the field of genetic breeding, can solve time-consuming and labor-intensive problems, and achieve simple and fast cost, low technical requirements, and the effect of expanding genetic resources
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Embodiment 1
[0052] 1.3 PCR amplification. to be detected F
[0053] 1.4 The above PCR products were detected by polyacrylamide gel electrophoresis. Configure 8% polypropylene gel, 180 volt electrophoresis 1.5
[0054] 1.5 Take out the above-mentioned polyacrylamide gel, silver staining, see Figure 1.
[0057] The F
Embodiment 2
[0064] 1.3 PCR amplification. to be detected F
[0065] 1.4 The above PCR products were detected by polyacrylamide gel electrophoresis. Configure 8% polypropylene gel, 180 volt electrophoresis 1.5
[0066] 1.5 Take out the above-mentioned polyacrylamide gel, silver staining, see Figure 3.
Embodiment 3
[0072] 1.1 Extract the genomic DNA of the plants to be tested and their parents.
[0076] 1.3 PCR amplification. Taking the plants to be detected and their parental DNAs as templates, PCR amplification reactions were carried out with the above primers. opposite
[0077] 1.4 The above PCR products were detected by polyacrylamide gel electrophoresis. Configure 8% polypropylene gel, 180 volt electrophoresis for 1 hour
[0078] 1.5 Take out the above-mentioned polyacrylamide gel, silver staining, see Figure 5.
[0081] Whole genome illumina sequencing was carried out to the No. 9 plant after the identification of the molecular markers, and the sequencing depth was 10 ×;
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