2007
DOI: 10.1007/978-1-59745-528-2_2
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OLIGO 7 Primer Analysis Software

Abstract: OLIGO performs a range of functions for researches in PCR and related technologies such as PCR and sequencing primer selection, hybridization probe design, inverse and real-time PCR, analysis of false priming using a unique priming efficiency (PE) algorithm, design of consensus and multiplex, nested primers and degenerate primers, reverse translation, and restriction enzyme analysis and prediction; based on a protein sequence, oligonucleotide database allows fully automatic multiplexing, primer secondary struc… Show more

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Cited by 359 publications
(220 citation statements)
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“…The primers were designed with Oligo (version 7, 2011) based on available bovine genomic sequences (GenBank accession numbers: ID A878328) (20 …”
Section: Dna Amplification With Pcr-rflpmentioning
confidence: 99%
“…The primers were designed with Oligo (version 7, 2011) based on available bovine genomic sequences (GenBank accession numbers: ID A878328) (20 …”
Section: Dna Amplification With Pcr-rflpmentioning
confidence: 99%
“…Agarose gel electrophoresis of the mtDNA sample with the total DNA showed no contamination from the chromosomal DNA. Based on the complete mtDNA sequences of F. catus (NC001700), A. jubatus (AY463959), and N. nebulosa (DQ257669), and some partial sequences of P. tigris (DQ151550), we successfully designed 34 pairs of primers for amplifying the complete mitochondrial genome sequences of the three species using Oligo 6.0 [21] (Table 1). PCR reactions were performed in an MJ Model PTC-200 thermal cycler with the following conditions: 95C for 5 min; 30 cycles of 94C for 50 s, 52C-56C for 1 min, 72C for 1 min; and 72C for 10 min.…”
Section: Samples Sources Dna Extraction and Pcr Amplificationmentioning
confidence: 99%
“…Experiment I: confirming the presence of specific sequences in genomic DNA To test whether the different combinations of flanking sequences were an artifact caused by enrichment procedures, or in fact occur in the observed association in the butterfly genome, we designed primers with OLIGO version 6 (Rychlik, 2000) to amplify 15 different combinations of symmetrical and asymmetrical sequence clusters in the ATG library. Product was detected with ethidium bromide-stained 1% agarose gel.…”
Section: Detection Of Inter-specific Homologiesmentioning
confidence: 99%