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Exact(8)
The introduction of the desired and the absence of off-target mutations was verified by sequencing.> -wrap-foot> The mutated sites are highlighted by italic bold letters.
The presence of all mutations was verified by sequence analysis.
The presence of the desired mutations was verified by sequencing the gene (BioS&T, Inc., Lachine, Canada) and by Q-ToF mass spectrometry (CBAMS, Concordia University, Canada).
Proper construction of the knockout mutations was verified by PCR (data not shown) using primers specific for the flanking regions of the targeted genes (Table 1).
Introduction of mutations was verified by DNA sequencing.
The presence of the mutations was verified by Sanger sequencing.
Similar(52)
In the mutant expression clones, the sequences of the entire region mutated were amplified by PCR and the expected mutations were verified by DNA sequencing.
The mutations were verified by sequencing.
All of the mutations were verified by DNA sequencing.
All mutations were verified by automatic sequencing (AGOWA, Germany).
All desired mutations were verified by sequence analysis.
More suggestions(15)
transfer was verified
mutant was verified
mutations was analyzed
mutations was based
mutations was performed
mutations was demonstrated
mutations was determined
mutations was observed
mutations was produced
mutations was designated
mutations was estimated
mutations were verified
mutations was found
mutations was calculated
mutations was identified
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