Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/13094
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dc.contributor.authorLi, Yanhe-
dc.contributor.authorWang, Weimin-
dc.contributor.authorLiu, Xiaolian-
dc.contributor.authorLuo, Wei-
dc.contributor.authorZhang, Jie-
dc.contributor.authorGul, Yasmeen-
dc.date.accessioned2011-11-30T09:34:54Z-
dc.date.available2011-11-30T09:34:54Z-
dc.date.issued2011-12-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/13094-
dc.description953-957en_US
dc.description.abstractCrayfish exoskeleton (CE) samples are generally less invasive and easy to be collected. However, it is difficult to extract DNA from them. This study was intended to investigate CE as a DNA source and design an easy and efficient DNA extraction protocol for polymerase chain reactions. Specific primer pair (PPO-F, PPO-R) was used to amplify extracted DNA from CE, and compared to crayfish tail muscle DNA sample. Moreover, seven microsatellites markers were used to amplify the CE DNA samples set. Since the extracted DNA from CE is suitable for gene amplification, the results present usefulness of CE as an easy and convenient DNA source for PCR-based population genetic research.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.49(12) [December 2011]en_US
dc.subjectCrayfish exoskeletonen_US
dc.subjectDNA amplificationen_US
dc.subjectDNA extractionen_US
dc.titleDNA extraction from crayfish exoskeletonen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.49(12) [December 2011]

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