References
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(3) Purelink PCR purification manual. http://products.invitrogen.com/ivgn/product/K220001(accessed July 11, 2016).
(4) AddGene, Plasmid Guide, DNA Ligation. http://www.addgene.org/plasmid_protocols/DNA_ligation/ (accessed July 11, 2016).
(5) Hanahan, D. 1983. Studies on transformation of Escherichia coli with plasmids. J.Mol.Biol. 1983, 166:557-580.
(6) Taylor, R. G.; Walker, D. C.; McInnes, R. R. E. coli host strains significantly affect the quality of small scale plasmid DNA preparations used for sequencing. Nucleic Acids Res. 1993, 21, 1677 -1678.
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Other references of interest:
a. Cohen, S. N.; Chang, A. C. Y.; Hsu, L. Nonchromosomal Antibiotic Resistance in Bacteria: Genetic Transformation of Escherichia coli by R-Factor DNA. Proc Natl Acad Sci U S A. 1972, 69, 2110–2114.
b. Yoshida, N.; Sato, M. Plasmid uptake by bacteria: a comparison of methods and efficiencies. Appl Microbiol Biotechnol. 2009, 83
c. Hanahan, D. DNA Cloning: A Practical Approach, ed. Glover, D.M., ed., Vol. 1, IRL Press,McLean, Virginia,; 1985; pp.109.
d. Inoue, H.; Nojima, H.; Okayama, H. High efficiency transformation of Escherichia coli with plasmids. Gene. 1990, 96, 23-28.
e. Hayashi, K.; Morooka, N.; Yamamoto, Y.; Fujita, K.; Isono, K.; Choi, S.; Ohtsubo, E.; Baba, T.;
f. Wanner, B. L.; Mori, H.; Horiuchi, T. (2006) “Highly accurate genome sequences of Escherichia coli
g. K- 12 strains MG1655 and W3110. Mol. Syst. Biol. 2006, 2, 1-5.