The apparent specificity of NotI (5′-GCGGCCGC-3′) is enhanced by M·FnuDII or M·BepI methyltransferases (5′-mCGCG-3′): cutting bacterial chromosomes into a few large pieces-Reference-Cited by-同舟云学术

The apparent specificity of NotI (5′-GCGGCCGC-3′) is enhanced by M·FnuDII or M·BepI methyltransferases (5′-mCGCG-3′): cutting bacterial chromosomes into a few large pieces

Published:1990-03 Issue:1 Volume:88 Page:101-105
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Qiang Bo-qin,McClelland Michael,Poddar Saibal,Spokauskas Alvydas,Nelson Michael

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference16 articles.

1. DNA methylation and the frequency of CpG in animal DNA;Bird;Nucleic Acids Res.,1980

2. CpG-rich islands and the function of DNA methylation;Bird;Nature,1986

3. Long-range restriction site mapping of mammalian genomic DNA;Brown;Nature,1986

4. Activity of restriction endonucleases and methylases in potassium glutamate (KGB);Hanish;Gene Anal. Tech.,1988

5. Cloning and structure of the M·BepI modification methyltransferase;Kuppur;Gene,1988

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1. The use of prokaryotic DNA methyltransferases as experimental and analytical tools in modern biology;Analytical Biochemistry;2005-03

2. Detection and Cloning of an X-Linked Locus Associated with a NotI Site That Is Not Methylated on Mouse Inactivated X Chromosome by the RLGS-M Method;Genomics;1999-10

3. Transgenic Cereals — Zea mays (maize);Molecular improvement of cereal crops;1999

4. Physical Mapping and Fingerprinting of Bacterial Genomes using Rare Cutting Restriction Enzymes;Bacterial Genomes;1998

5. Restriction Endonucleases and Modification Methylases;Enzymology Primer for Recombinant DNA Technology;1996