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http://nopr.niscpr.res.in/handle/123456789/13094
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DC Field | Value | Language |
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dc.contributor.author | Li, Yanhe | - |
dc.contributor.author | Wang, Weimin | - |
dc.contributor.author | Liu, Xiaolian | - |
dc.contributor.author | Luo, Wei | - |
dc.contributor.author | Zhang, Jie | - |
dc.contributor.author | Gul, Yasmeen | - |
dc.date.accessioned | 2011-11-30T09:34:54Z | - |
dc.date.available | 2011-11-30T09:34:54Z | - |
dc.date.issued | 2011-12 | - |
dc.identifier.issn | 0975-1009 (Online); 0019-5189 (Print) | - |
dc.identifier.uri | http://hdl.handle.net/123456789/13094 | - |
dc.description | 953-957 | en_US |
dc.description.abstract | Crayfish 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.iso | en_US | en_US |
dc.publisher | NISCAIR-CSIR, India | en_US |
dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
dc.source | IJEB Vol.49(12) [December 2011] | en_US |
dc.subject | Crayfish exoskeleton | en_US |
dc.subject | DNA amplification | en_US |
dc.subject | DNA extraction | en_US |
dc.title | DNA extraction from crayfish exoskeleton | en_US |
dc.type | Article | en_US |
Appears in Collections: | IJEB Vol.49(12) [December 2011] |
Files in This Item:
File | Description | Size | Format | |
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IJEB 49(12) 953-957.pdf | 558.1 kB | Adobe PDF | View/Open |
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