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We amplified aqpM by PCR from M. marburgensis DNA.
We amplified multiple BORIS RT-PCR products that were then cloned and sequenced (Fig. 1C).
We amplified and sequenced a 994 bp fragment of the voltage-gated sodium channel (VGSC) gene.
We amplified and sequenced the cDNAs coding each allozymatic lysozyme expressed in eggs and salivary glands.
We amplified and sequenced a set of 60 large exons, plus 17 gene fragments including introns.
We amplified and sequenced the region of R882 and C709.
We amplified by nested PCR and sequenced the cytb gene (6 ).
We amplified and sequenced this fragment using the primers L15774 and H16498 [ 53].
We amplified fragments of the Hox clusters with a combination of LA PCR and GW.
We amplified part of the S gene to study the variability of our isolates.
We amplified mtDNA using 32 overlapping fragments as described elsewhere [ 40].
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