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We used partial sequences of five independent WRKY loci to assess their potential for phylogeny reconstruction.
Partial sequences of the Date-SRY were taken and amplified by nested polymerase chain reaction (PCR).
Only 25 unique partial sequences of msp-2 were found in 61 isolates examined.
Partial sequences of feline mRNAs had 86 95% identity with dog and human genes.
The partial sequences of ITS rRNA genes allowed for the identification of the strains.
Partial sequences of ISPa41 were also present in P.putida F1, S16 and W619.
PCR primers were designed based on partial sequences of the 16S rDNA genes of oral Rothia species.
For this, conserved regions resulting from the alignment of 26 published partial sequences of such gene were used.
Five partial sequences of PgAFP were obtained by Edman degradation and by ESI-MS/MS after trypsin and chymotrypsin digestions.
Partial sequences of the cestode nad1 gene were aligned and new primers were designed based on conserved regions.
Pure isolates containing lipophilic inclusions were identified based on microscopy and by sequencing partial sequences of their 16SrRNA.
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