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Electron. j. biotechnol ; Electron. j. biotechnol;11(2): 126-129, Apr. 2008. ilus, tab
Artículo en Inglés | LILACS | ID: lil-522210

RESUMEN

Developing countries are facing severe bottlenecks in the technological advancement in biotechnology, due to restrictions imposed by patent protected products and protocols. This calls for designing of simple and cost-effective alternatives for the indispensable products like DNA molecular weight markers. We demonstrate a novel, rapid and cost-effective method of making in-house 100bp ladder for routine use. In our method we use a single forward primer and five reverse primers designed on the backbone sequence of a commonly used vector template. These primers are used at a universal annealing temperature to amplify ten DNA fragments of accurate size ranging from 100bp to 1000bp. Our PCR-based method can provide size standards for an endless usage.


Asunto(s)
Marcadores Genéticos , Estándares de Referencia , Moldes Genéticos , Biotecnología , Vectores Genéticos , Reacción en Cadena de la Polimerasa
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