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Effective DNA extraction method for fragment analysis using capillary sequencer of the kelp, Saccharina
Authors:Takashi Maeda  Tadashi Kawai  Masahiro Nakaoka  Norishige Yotsukura
Institution:1. Graduate School of Environmental Science, Hokkaido University, Hokkaido, 060-0810, Japan
2. Wakkanai Fisheries Experimental Station, Hokkaido Research Organization, Hokkaido, 097-0001, Japan
3. Akkeshi Marine Station, Hokkaido University, Hokkaido, 088-1113, Japan
4. Field Science Center for Northern Biosphere, Hokkaido University, Hokkaido, 060-0809, Japan
Abstract:Deoxyribonucleic acid (DNA) fragment analysis can become an effective tool to study genetic differences between species and individuals on saccharinan kelp from which the little genetic diversity has been reported. Here, extraction methods of DNA suitable for use in analysis with a capillary sequencer is examined on Saccharina japonica var. diabolica which contains abundant polysaccharide. When amplified fragment length polymorphism was performed using genomic DNA extracted by seven different methods: (1) commercial kit, (2) original cetyl trimethylammonium bromide (CTAB) method, (3)–(5) three types of modified CTAB method, (6) modified sodium dodecyl sulfate (SDS) method, (7) combination of CTAB method and SDS method, a high reproducible peak that was suitable for analysis was noticeable in the electropherogram in the experiment with the last combination method (7). It is considered that the pretreatment washing of polysaccharide and the subsequent purification for protein and ribonucleic acid in SDS method and for polysaccharide in CTAB method are effective to obtain the high-purity DNA.
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