Method for screening fine progeny strain polyploidy plant of Chinese gooseberry Hort 16A
A Chinese kiwifruit, hort16a technology, applied in the field of plant genetics and breeding, can solve the problems of uncertainty, heavy workload, and many influencing factors, and achieve the effect of significant progress, easy access, and significant substantive characteristics.
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[0037] (1) Extract the total RNA from the leaves of Actinidia sinensis tissue cultured seedlings using the Plant RNA Rapid Extraction Kit. Under the conditions of 1.0% agarose gel, 110V voltage, and electrophoresis for 25 minutes, the quality of the extracted total RNA was detected to observe whether the bands were clear, whether there was degradation, and whether there was DNA contamination.
[0038] (2) Prepare the reaction solution to remove genomic DNA (see Table 4), then prepare the reaction system (the mixture is prepared on ice, see Table 5), reverse transcribe the RNA into cDNA, and use the reverse transcription product for PCR amplification:
[0039] Table 4 Removal of Genomic DNA Reaction System
[0040]
[0041] Gently blow and mix with a pipette, inactivate DNase I at 37°C for 30 min; at 65°C for 10 min.
[0042] Table 5 Reaction system for reverse transcription of RNA into cDNA
[0043]
[0044] The setting of reverse transcription reaction conditions: 25°...
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