Enhanced capacity for electrophoretic capture of plasmid DNA by agarase treatment of agarose gels

Biomacromolecules

Volumn 1, Issue 4, 2000, Pages 771-781

  Cole, Kenneth D ^a,b   Åkerman, Björn ^a,b  

^a NATIONAL INSTITUTE OF STANDARDS AND TECHNOLOGY   (United States)

^b CHALMERS UNIVERSITY OF TECHNOLOGY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

AGARASE; CIRCULAR DNA; DNA; GLYCOSIDASE; SEPHAROSE;

AGAR GEL ELECTROPHORESIS; ARTICLE; CHEMISTRY; ISOLATION AND PURIFICATION; METHODOLOGY; MOLECULAR WEIGHT; PLASMID; POROSITY;

DNA; DNA, CIRCULAR; ELECTROPHORESIS, AGAR GEL; GLYCOSIDE HYDROLASES; MOLECULAR WEIGHT; PLASMIDS; POROSITY; SEPHAROSE;

EID: 0034570961     PISSN: 15257797     EISSN: None     Source Type: Journal    
DOI: 10.1021/bm005594c     Document Type: Article

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23. Certain commercial equipment, instruments, or materials are identified in this paper to specify adequately the experimental procedures. Such identification does not imply recommendation by NIST, nor does it imply that the materials or equipment are necessarily the best available for the purpose.