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The two-step gene walking method consisted of a walking-PCR (step 1) followed by direct sequencing of the PCR product (step 2) [ 17].
Fig. 1 The genome walking method scheme.
To amplify the flanking sequences that are adjacent to Tn5 transposon insertion sites in Serratia marcescens FZSF02, we developed a genome walking method based on TAIL-PCR.
In the present work, a PCR based genome walking method was adopted to isolate and clone the promoter for the NMT gene.
Near full-length genome of the construct was sequenced using primer walking method described previously [6].
The primer walking method was used to finish insert sequencing, with primers automatically designed by PRIDE [23].
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These newly developed DNA walking methods are completing the previously implemented DNA walking method targeting the t35S pCAMBIA element.
Previously, we proposed a walking method named the "leg-grope walk" method, and discussed the validity of this strategy based on our experiments on a fragile horizontal plane [21].
using the Primer-Walking method.
The genome-walking method has attracted some attention.
Then, a contiguous sequence extended to 3,200-bp 3,200-bps obtained by gluome-wasking methobtained
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