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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
15
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pubmed:dateCreated |
1988-10-5
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pubmed:abstractText |
Quantitative measurement of DNA migration in gel electrophoresis requires precisely controlled homogeneous electric fields. A new electrophoresis system has allowed us to explore several parameters governing DNA migration during homogeneous field pulsed field gel (PFG) electrophoresis. Migration was measured at different switch times, temperatures, agarose concentrations, and voltage gradients. Conditions which increase DNA velocities permit separation over a wider size range, but reduce resolution. We have also varied the angle between the alternating electric fields. Reorientation angles between 105 degrees and 165 degrees give equivalent resolution, despite significant differences in DNA velocity. Separation of DNA fragments from 50 to greater than 7000 kilobases (Kb) can easily be optimized for speed and resolution based on conditions we describe.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-2880670,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-2954030,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-2959907,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3295780,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3431469,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3520483,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3538420,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3601680,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3627974,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-3952500,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-4069202,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-6373014,
http://linkedlifedata.com/resource/pubmed/commentcorrection/3412895-6379602
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0305-1048
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
11
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7563-82
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pubmed:dateRevised |
2010-9-9
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pubmed:meshHeading |
pubmed-meshheading:3412895-Chromosomes,
pubmed-meshheading:3412895-DNA,
pubmed-meshheading:3412895-DNA, Fungal,
pubmed-meshheading:3412895-DNA, Viral,
pubmed-meshheading:3412895-Electricity,
pubmed-meshheading:3412895-Electrophoresis,
pubmed-meshheading:3412895-Electrophoresis, Agar Gel,
pubmed-meshheading:3412895-Molecular Weight,
pubmed-meshheading:3412895-Schizosaccharomyces,
pubmed-meshheading:3412895-Time Factors
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pubmed:year |
1988
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pubmed:articleTitle |
Optimized conditions for pulsed field gel electrophoretic separations of DNA.
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pubmed:affiliation |
Division of Biology, California Institute of Technology, Pasadena 91125.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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