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30 PLAP binding clones were detected.
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Of ∼2.2 × 10 and ∼2.0 × 10 clones tested, 35 and 32 positive interacting clones were detected as putative binding partners of E47 and E12, respectively.
Three weeks later, positive clones were detected by Western blotting after culture expansion.
Twenty-eight 16S rRNA gene-containing archaeal clones and sixteen bacterial clones were detected in the library.
A total of 13 positive clones were detected.
Only 4 clones were detected in more than one hospital.
Of ∼1.7 × 10 clones screened, 127 positive interacting clones were detected.
Only 4 clones from 107 clones were detected in more than one hospital (Table 2).
These methods alone are extracted separately and by checking external behaviour, type-4 clones are detected.
Neither clone was detected at 39 sites (44.3%).
A number of candidates with low binding energy were detected.
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