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# Downsample a time sequence.
Restriction digestion, PCR amplification and/or sequencing were carried out to ensure sequence integrity and orientation.
Sanger sequencing was performed on DN-1 and DN-2 virus stocks to ensure sequence integrity prior to experiments, with sequencing performed on PCR amplification fragments generated using primers in Supplementary Table 1.
The sequence integrity of all constructs described in this study was verified for sequence integrity by nucleotide sequencing.
All the plasmids containing CmADH genes were sequenced to verify sequence integrity (AuGCT, Beijing, China).
Sequence integrity was verified using Sanger sequencing.
Sequence integrity was verified by sequencing.
All vectors were sequenced to ensure sequence integrity.
All PCR products were sequenced to confirm their sequence integrity.
Plasmid containing the promoter of znuC (pGT- znuCp) was sequenced to verify sequence integrity.
Successful insertion and sequence integrity were confirmed using restriction digestion and DNA sequencing.
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