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The mitogenomes were amplified in their entirety using a long PCR technique [73].
The mitogenomes were amplified in their entirety using a long PCR technique [ 69].
We amplified the mitogenomes of the 33 lophiiform species in their entirety using a long PCR technique [ 42].
The mitogenomes of the three Asymmetron species were amplified in their entirety using a long PCR technique.
Briefly, the mitogenomes of the 51 otophysans in their entirety were amplified using a long PCR technique [ 46] in two or three reactions.
We amplified whole mitogenome sequences for the 11 labroids plus a single non-labroid species (Labracinus cyclophthalma: Pseudochromidae) using a long PCR technique [ 37].
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We encountered DNA samples which showed a positive product using a long PCR-based method for the detection of CYP2D6*5, indicating deletion of the entire CYP2D6 gene, but the samples did not show a band related to CYP2D6*5 in either XbaI- or EcoRI-RFLP analysis.
The mtDNA of each species was amplified using a long-PCR technique with LA-Taq (Takara).
We chose to use a long-PCR whole plastome amplification approach to maximize the number of reads to be used for assembly.
PCR analyses that bridged the genomic breakpoints were performed by using a long-range PCR polymerase mix (Fermentas, St Leon-Rot, Leon-Rot, Germanyg to the maccordinger's descriptoon.
Sanger library construction The entire chloroplast sequence was amplified using a long-range PCR technique with cpDNA.
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