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RAPID ISOLATION OF SOYBEAN DNA FOR PCRWITH LARGE NUMBERS OF SMALL SAMPLES(PDF)

《大豆科学》[ISSN:1000-9841/CN:23-1227/S]

Issue:
1999年04期
Page:
318-321
Research Field:
Publishing date:

Info

Title:
RAPID ISOLATION OF SOYBEAN DNA FOR PCRWITH LARGE NUMBERS OF SMALL SAMPLES
Author(s):
Zhou Si jun
Biotechnolog y Research Center, Heilongjiang Academyof Agricul tural Sciences, Harbin, 150086
Keywords:
Soybean PCR DN A isolation
PACS:
-
DOI:
10.11861/j.issn.1000-9841.1999.04.0318
Abstract:
The problem of grinding large numbers of small samples of f resh soy bean ti ssues rapidlyand w ithout loss w as solv ed by using a g rinder modified w ith a spiral ratchet screw driv er.The effect of different ex traction buffers, different temperatures and dif ferent t reatmenttimes on the quality of DN A w ere compared by ex amining the DN A with random- primerPCR. The result show ed that soy bean templet DN A suitable for PCR reaction could be gottenby using SDS ex traction buffer, 5 minutes treatment wi th 65- 80℃ and one time of extractionwith chloroform and iso- amy l alcohol. DN A was isola ted f rom mo re than a thousandsoybean samples wi th this procedure. The effect was stable.

References:

[1 ] Hong Wang et al. 1993. A simple method of preparing plan t samples f or PCR. Nucleic Acids Res, 21( 7): 4153-4154

[2 ] Oard JD et al. 1992. Rapid i solation of rice and maize DN A f or analysi s by rand om- p rimer PCR. Plant MolecularBiology Report er, 10: 234- 241
[3 ] St ew ard Jr. CN. 1994. Soybean DNA i solation p roced ure using f resh tissue. Soybean Gen etics New slet t er, 21:243- 244
[4 ] Robert GB. 1997. Plant t ransf ormati on: problems and st rat egies for p ractical applicati on. Annual Review ofPlant Physi ology and Plant Molecular Biology, 48: 297- 326

Memo

Memo:
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Last Update: 2016-12-27