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Exact(20)
In, addition, 61 and 54 mutants were sequenced in control and exposed groups, respectively.
Randomly selected transposon carrying protease negative mutants were sequenced and alignment of these sequences lead to the identification of the protease open reading frame (ORF).
The mutants were sequenced, and we verified by western blotting that the proteins expressed had the expected size.
The TBCD mutants were sequenced and cloned into the pEGFP-C2 and/or pEGFP-N3 vectors from Invitrogen (Life technologies, California USA).
All mutants were sequenced to verify the intended mutation.
The protein coding region of all chimeras and mutants were sequenced.
Similar(40)
The glpT gene of all mutants was sequenced, and compared with the wild type gene as described [37].
In addition, a library of 100 random mutants was sequenced to determine our ability to detect unique mutations.
The region flanking the transposon insertion in each mutant was sequenced and compared with the sequenced genome of Xcc strain 8004.
The genome of the mutant was sequenced to ensure the successful insertion of the DNA fragments into the Mtb genome.
The open reading frame of each mutant was sequenced entirely.
More suggestions(15)
shifts were sequenced
mutants were confirmed
mutants were obtained
mutants were recovered
mutants was sequenced
mutants were discovered
mutants were set
mutants were generated
mutants were monitored
mutants were indicated
mutants were named
mutants were affected
mutants were expressed
mutants were designed
mutants were solved
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