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Three newer collected Polish common osier clones, and three clones from Swedish cultivars of common osier, were also used in this study.
All of the EcoRI X clones and three of the EcoRI c clones contained a 30-base-pair (bp) sequence which was directly repeated at the ends of the MCMV genome.
Seven MaSp1-positive clones and three MaSp2-positive clones were found after screening half of the library.
Similarly, 168 sequences of 102 shotgun clones and three PCR products were used to assemble the 27.9-kb scaffold containing the OnubOR5c-4 genes.
The results were reproduced with two different antibody clones and three different fluorochromes.
We tested all combinations of 14 D. magna clones and three P. ramosa clones for spore activation (Table 1).
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Twenty Vα2+, CD4+ clones and twenty Vα2−, CD4− clones were selected and used for further studies.
Among the sequenced clones, the three major genotypes again were well represented with 51 VT-like clones, twelve T30-like clones, and six T36-like clones.
Cluster B contained the sequences of six clones and one xylanase directly cloned from an uncultured human gut bacterium.
Twenty-eight 16S rRNA gene-containing archaeal clones and sixteen bacterial clones were detected in the library.
Overall, five different female clones and nine different male clones were used in the experiments (Table 1).
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