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We also evaluate the correlation with the expected amino acid pair scores obtained when the sequences are aligned using a classic nucleotide match/mismatch system.
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Using a classic codesign approach.
BAL was performed using a classic protocol.
These conditions can be illustrated using a classic example.
The four pairwise comparisons were made using a classic Fisher exact test.
The cell concentration and the viability were determined using a classic dye exclusion method (Trypan Blue).
We used a classic typing scheme to determine the lineage of 107 isolates from various hosts.
Peptides were extracted and analysed by LC-MS/MS using an Orbitrap Classic mass spectrometer (Thermo Scientific).
Data was acquired using an Odyssey Classic infra-red imager (Li-Cor Biosciences).
The PCR products were purified using a QIAGEN MinElute PCR Purification Kit to remove unincorporated primers and nucleotides.
Nucleotide binding was measured using a standard filter-binding assay.
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