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Additionally, after unsuccessful amplifications, two shorter fragments of 75 and 102 bp were also tested in order to account for possible DNA degradation.
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Since these noninvasive procedures have different working mechanism from Bps, the synergic efficacies of two treatments, like ESWT combined with oral Bps, were also tested in recent studies [ 31, 32].
The clinical validity of SG-BP, contrary to K-BP, was also tested by correlating their time-change with markers of vascular disease and vascular risk factors.
In addition to BPs, another polysaccharides extracted from BCPs were also tested in our ELISA assay to study its inhibitory effect on the LP.
A 100 bp dsDNA substrate and 100-nucleotide ssDNA oligonucleotides were also tested, although none gave higher proportions of mixed plaques than the 200 bp dsDNA substrate (Table 1).
The 55 PBSA emulsion-degrading strains were also tested for their ability to produce BP- degrading enzyme by cultivating them in liquid FMZ medium.
Samples were also tested at the ospC locus, using a nested-PCR protocol that produced an approximately 500-bp ospC fragment (47).
The response of the PBR to 4-BP shock loadings was also tested, and the bioreactor was found to adequately handle these shock loadings.
Organic chicken was also tested.
In addition, the spline-window method was also tested using the W statistics to compare between windows of unequal size with GCV and a resolution of 100 bp.
The ESTs were further tested for vector sequence contamination using NCBI VecScreen; ESTs of less than 300 bp were also discarded.
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