「Medlin Elwood Stickel Sogin 1988」の版間の差分

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=Medlin et al. (1988)=
 
=Medlin et al. (1988)=
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== 文献(出典)==
 
*Medlin, L., Elwood, H. J., Stickel, S. & Sogin, M. L.  1988.  The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions.  Gene 71: 491-499.
 
*Medlin, L., Elwood, H. J., Stickel, S. & Sogin, M. L.  1988.  The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions.  Gene 71: 491-499.
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==ノート==
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==Abstract==
 
==Abstract==
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Polymerase chain reaction conditions were established for the in vitro amplification of eukaryotic small subunit ribosomal (16S-like) rRNA genes.  Coding regions from algae, fungi, and protozoa were amplified from nanogram quantities of genomic DNA or recombinant plasmids containing rDNA genes.  Oligodeoxynucleotides that are complementary to conserved regions at the 5' and 3' termini of eukaryotic 16S-like rRNAs were used to prime DNA synthesis in repetitive cycles of denaturation, reannealing, and DNA synthesis.  The fidelity of synthesis for the amplification products was evaluated by comparisons with sequences of previously reported rRNA genes or with primer extension analyses of rRNAs.  Fewer than one error per 2000 positions were observed in the amplified rRNA coding region sequences.  The primary structure of the 16S-like rRNA from the marine diatom, ''Skeletonema costatum'', was inferred from the sequence of its in vitro amplified coding region.
 
Polymerase chain reaction conditions were established for the in vitro amplification of eukaryotic small subunit ribosomal (16S-like) rRNA genes.  Coding regions from algae, fungi, and protozoa were amplified from nanogram quantities of genomic DNA or recombinant plasmids containing rDNA genes.  Oligodeoxynucleotides that are complementary to conserved regions at the 5' and 3' termini of eukaryotic 16S-like rRNAs were used to prime DNA synthesis in repetitive cycles of denaturation, reannealing, and DNA synthesis.  The fidelity of synthesis for the amplification products was evaluated by comparisons with sequences of previously reported rRNA genes or with primer extension analyses of rRNAs.  Fewer than one error per 2000 positions were observed in the amplified rRNA coding region sequences.  The primary structure of the 16S-like rRNA from the marine diatom, ''Skeletonema costatum'', was inferred from the sequence of its in vitro amplified coding region.
  
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==要旨==
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==Pdf==
 
*https://epic.awi.de/13936/1/Med1988a.pdf
 
*https://epic.awi.de/13936/1/Med1988a.pdf
  
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[[Category:1988]]
 
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[[Category:M]]
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[[Category:文献]]
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[[Category:植物]]
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[[Category:PCR]]
 
[[Category:primer]]
 
[[Category:primer]]

2015年12月27日 (日) 22:09時点における最新版

目次

Medlin et al. (1988)

文献(出典)

  • Medlin, L., Elwood, H. J., Stickel, S. & Sogin, M. L. 1988. The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions. Gene 71: 491-499.

ノート

Abstract

Medlin, L., Elwood, H. J., Stickel, S. & Sogin, M. L. 1988. The characterization of enzymatically amplified eukaryotic 16S-like rRNA-coding regions. Gene 71: 491-499.

Polymerase chain reaction conditions were established for the in vitro amplification of eukaryotic small subunit ribosomal (16S-like) rRNA genes. Coding regions from algae, fungi, and protozoa were amplified from nanogram quantities of genomic DNA or recombinant plasmids containing rDNA genes. Oligodeoxynucleotides that are complementary to conserved regions at the 5' and 3' termini of eukaryotic 16S-like rRNAs were used to prime DNA synthesis in repetitive cycles of denaturation, reannealing, and DNA synthesis. The fidelity of synthesis for the amplification products was evaluated by comparisons with sequences of previously reported rRNA genes or with primer extension analyses of rRNAs. Fewer than one error per 2000 positions were observed in the amplified rRNA coding region sequences. The primary structure of the 16S-like rRNA from the marine diatom, Skeletonema costatum, was inferred from the sequence of its in vitro amplified coding region.

要旨

Pdf


広島大学 / デジタル自然史博物館 / 植物 にもどる