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A positive TAC clone (ZR1) was obtained and confirmed by sequence analysis.
We also show evidence that Rrp40p can bind RNA in vitro, as predicted by sequence analysis.
Conserved regulatory elements were identified in the ppyk20 by sequence analysis.
Yeast isolates were identified by sequence analysis of 18S rRNA gene.
The isolates were identified by sequence analysis of 16S rRNA genes.
Selected fungal isolates were also identified by sequence analysis of rDNA gene.
These were verified by sequence analysis.
The presence of all mutations was verified by sequence analysis.
All desired mutations were verified by sequence analysis.
The insertion sites were determined by sequence analysis.
The integrity of all constructs was confirmed by sequence analysis.
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