Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction
An efficient DNA extraction method was developed for peanut seed, where only 3-5 mg cotyledonary tissue was enough for more than 50 PCR reactions with a reaction volume of 15 μl. Both low copy number and high copy number DNA sequences were successfully amplified. Processing one seed sample...
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Pontificia Universidad Católica de Valparaíso
2010
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oai:scielo:S0717-345820100004000122010-08-04Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain ReactionYu,Shu TaoWang,Chuan TangYu,Shan LinWang,Xiu ZhenTang,Yue YiChen,Dian XuZhang,Jian Cheng cotyledonary tissue DNA extraction groundnut PCR peanut An efficient DNA extraction method was developed for peanut seed, where only 3-5 mg cotyledonary tissue was enough for more than 50 PCR reactions with a reaction volume of 15 μl. Both low copy number and high copy number DNA sequences were successfully amplified. Processing one seed sample only took about half an hour. Sampling had no significant effects on germination and development. The DNA extraction method makes it possible to identify transformants and conduct molecular marker studies prior to sowing, and thus may greatly hasten research progress.info:eu-repo/semantics/openAccessPontificia Universidad Católica de ValparaísoElectronic Journal of Biotechnology v.13 n.4 20102010-07-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582010000400012en |
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English |
topic |
cotyledonary tissue DNA extraction groundnut PCR peanut |
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cotyledonary tissue DNA extraction groundnut PCR peanut Yu,Shu Tao Wang,Chuan Tang Yu,Shan Lin Wang,Xiu Zhen Tang,Yue Yi Chen,Dian Xu Zhang,Jian Cheng Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
description |
An efficient DNA extraction method was developed for peanut seed, where only 3-5 mg cotyledonary tissue was enough for more than 50 PCR reactions with a reaction volume of 15 μl. Both low copy number and high copy number DNA sequences were successfully amplified. Processing one seed sample only took about half an hour. Sampling had no significant effects on germination and development. The DNA extraction method makes it possible to identify transformants and conduct molecular marker studies prior to sowing, and thus may greatly hasten research progress. |
author |
Yu,Shu Tao Wang,Chuan Tang Yu,Shan Lin Wang,Xiu Zhen Tang,Yue Yi Chen,Dian Xu Zhang,Jian Cheng |
author_facet |
Yu,Shu Tao Wang,Chuan Tang Yu,Shan Lin Wang,Xiu Zhen Tang,Yue Yi Chen,Dian Xu Zhang,Jian Cheng |
author_sort |
Yu,Shu Tao |
title |
Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
title_short |
Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
title_full |
Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
title_fullStr |
Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
title_full_unstemmed |
Simple method to prepare DNA templates from a slice of peanut cotyledonary tissue for Polymerase Chain Reaction |
title_sort |
simple method to prepare dna templates from a slice of peanut cotyledonary tissue for polymerase chain reaction |
publisher |
Pontificia Universidad Católica de Valparaíso |
publishDate |
2010 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-34582010000400012 |
work_keys_str_mv |
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