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Banding patterns were obtained by random amplification of polymorphic DNA (RAPD), and specific D9S50 and D9S52 microsatellites (9p21).
To identify differentially expressed transcripts, electrophoretic banding patterns were obtained from cDNAs.
SmaI/ cfr9I-digested DNA banding patterns were obtained by pulsed-field gel electrophoresis for clone identification as described (4 ).
Apart from this, different DNA banding patterns were obtained by ERIC-PCR from positive strains, which means that most of them were not clonally related.
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Unique band patterns were obtained with virtual PCR performed on the whole genome sequences of the two reference strains.
For four bat samples, identical DNA band patterns were obtained for ITS-PCR analysis from matching tissues and pure cultures (Fig. 4A).
A similar banding pattern was obtained for PS2 complexes in CSF using the PS2-CTF antibody 00/12; PS2 fragments having similar high molecular mass as PS1 [ 7, 11].
A clear and easily discriminated band pattern was obtained for all five types.
C34, on the other hand, can run through the gel and a distinct band pattern is obtained.
In the chosen low stringency conditions complex patterns were obtained, with a sharp band of ∼700 bp in cases where the vanA gene was present.
Fourteen different DRE-PCR patterns were obtained with a range of two to eight bands.
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