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PLoS One ; 7(4): e34373, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22493688

RESUMO

Here we introduce a rapid, cost-effective method of generating molecular DNA probes in just under 15 minutes without the need for expensive, time-consuming gel-extraction steps. As an example, we enzymatically concatenated six variable strands (50 bp) with a common strand sequence (51 bp) in a single pool using Fast-Link DNA ligase to produce 101 bp targets (10 min). Unincorporated species were then filtered out by passing the crude reaction through a size-exclusion column (<5 min). We then compared full-length product yield of crude and purified samples using HPLC analysis; the results of which clearly show our method yields three-quarters that of the crude sample (50% higher than by gel-extraction). And while we substantially reduced the amount of unligated product with our filtration process, higher purity and yield, with an increase in number of stands per reaction (>12) could be achieved with further optimization. Moreover, for large-scale assays, we envision this method to be fully automated with the use of robotics such as the Biomek FX; here, potentially thousands of samples could be pooled, ligated and purified in either a 96, 384 or 1536-well platform in just minutes.


Assuntos
Sondas de DNA/isolamento & purificação , DNA de Cadeia Simples/isolamento & purificação , Oligodesoxirribonucleotídeos/isolamento & purificação , Sequência de Bases , Cromatografia em Gel , Cromatografia Líquida de Alta Pressão , Análise Custo-Benefício , DNA Ligase Dependente de ATP , DNA Ligases/metabolismo , Sondas de DNA/biossíntese , Sondas de DNA/economia , DNA de Cadeia Simples/biossíntese , DNA de Cadeia Simples/economia , Dados de Sequência Molecular , Oligodesoxirribonucleotídeos/biossíntese , Oligodesoxirribonucleotídeos/economia
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