Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/3888
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dc.contributor.authorPatel, Darshan H-
dc.contributor.authorWi, Seung Gon-
dc.contributor.authorBae, Hyeun Jong-
dc.date.accessioned2009-04-17T10:13:42Z-
dc.date.available2009-04-17T10:13:42Z-
dc.date.issued2009-04-
dc.identifier.issn0972-5849-
dc.identifier.urihttp://hdl.handle.net/123456789/3888-
dc.description183-186en_US
dc.description.abstractIn vitro site-directed repair or creation of a mutation is an invaluable technique in genetic and protein engineering. Several methods have appeared in literature but still require many modifications. We describe a rapid and efficient modified overlap extension PCR method for multiple uses in mutagenesis studies. The protocol is based on two rounds of PCR with the help of two sets of primers, two flanking and two internal mutagenic primers. Two fragments of DNA prepared in first round of PCR are then allowed themselves to anneal in the second stage of PCR using gradient annealing temperature without using flanking primers. This protocol has been used for correcting a mutation caused in exoglucanase (CBHII) gene of Trichoderma spp. We successfully synthesized the full length of gene from two fragments in the second round of PCR in lesser time.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJBT Vol.8(2) [April 2009]en_US
dc.subjectDNA polymeraseen_US
dc.subjectex taqen_US
dc.subjectoverlap extension PCRen_US
dc.subjectsite directed mutagenesisen_US
dc.subjectone step overlap extension-PCRen_US
dc.titleModification of overlap extension PCR: A mutagenic approachen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.08(2) [April 2009]

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