Molecular markers for identification of a10 and c07 chromosome segregation in hybrids between Chinese cabbage and Ethiopian mustard and their progeny
A technology of molecular markers and chromosomes, applied in the field of genetic breeding, can solve time-consuming and labor-intensive problems, and achieve the effect of simple and fast cost, low technical requirements, and expansion of genetic resources
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Embodiment 1
[0045] 1.3 PCR amplification. to be detected F
[0046] 1.4 The above PCR products were detected by polyacrylamide gel electrophoresis. Configure 8% polypropylene gel, 180 volt electrophoresis 1‑2
[0047] 1.5 Take out the above-mentioned polyacrylamide gel, and stain with silver for color development.
Embodiment 2
[0054] 1.1 Extract the genomic DNA of the plants to be tested and their parents.
[0058] 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
[0059] 1.4 The above PCR products were detected by polyacrylamide gel electrophoresis. Configure 8% polypropylene gel, 180 volt electrophoresis for 2 hours
[0060] 1.5 Take out the above-mentioned polyacrylamide gel, silver staining, see Figure 3.
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