Amplified insert assembly: an optimized approach to standard assembly of BioBrickTM genetic circuits
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[1] N. Daraselia,et al. NOMAD: a versatile strategy for in vitro DNA manipulation applied to promoter analysis and vector design. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[2] G. Bennett,et al. Formation of MboII vectors and cassettes using asymmetric MboII linkers. , 1987, Gene.
[3] Thomas F. Knight,et al. Idempotent Vector Design for Standard Assembly of Biobricks , 2003 .
[4] Drew Endy,et al. Engineering BioBrick vectors from BioBrick parts , 2008, Journal of Biological Engineering.
[5] D. Hanahan. Studies on transformation of Escherichia coli with plasmids. , 1983, Journal of molecular biology.
[6] A. D. Kaiser,et al. Enzymatic end-to end joining of DNA molecules. , 1973, Journal of molecular biology.
[7] A. C. Chang,et al. Construction of biologically functional bacterial plasmids in vitro. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[8] Ira Phillips,et al. A New Biobrick Assembly Strategy Designed for Facile Protein Engineering , 2006 .
[9] R. W. Davis,et al. Cleavage of DNA by R 1 restriction endonuclease generates cohesive ends. , 1972, Proceedings of the National Academy of Sciences of the United States of America.
[10] Z. Topçu. An optimized recipe for cloning of the polymerase chain reaction-amplified DNA inserts into plasmid vectors. , 2000, Acta biochimica Polonica.
[11] I. Zabin. β-Galactosidase α-complementation , 1982, Molecular and Cellular Biochemistry.
[12] R. Tsien,et al. A monomeric red fluorescent protein , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[13] P. Dreze,et al. Positive selection vectors to generate fused genes for the expression of his-tagged proteins. , 1998, BioTechniques.
[14] D. Endy. Foundations for engineering biology , 2005, Nature.
[15] I. Zabin. beta-Galactosidase alpha-complementation. A model of protein-protein interaction. , 1982, Molecular and cellular biochemistry.
[16] D. G. Gibson,et al. Enzymatic assembly of DNA molecules up to several hundred kilobases , 2009, Nature Methods.
[17] Jay D Keasling,et al. BglBricks: A flexible standard for biological part assembly , 2010, Journal of biological engineering.
[18] S. Ho,et al. Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. , 1989, Gene.
[19] P. Bernard,et al. Positive selection of recombinant DNA by CcdB. , 1996, BioTechniques.
[20] P. Modrich,et al. Recognition sequence of the dam methylase of Escherichia coli K12 and mode of cleavage of Dpn I endonuclease. , 1979, The Journal of biological chemistry.
[21] Reshma Shetty,et al. Article Title: Assembly of Biobrick Standard Biological Parts Using Three Antibiotic Assembly , 2022 .
[22] M. Uhlén,et al. A general strategy for polymerization, assembly and expression of epitope-carrying peptides applied to the Plasmodium falciparum antigen Pf155/RESA. , 1990, Gene.
[23] D. Endy,et al. Refinement and standardization of synthetic biological parts and devices , 2008, Nature Biotechnology.
[24] M. Hynes,et al. Versatile suicide vectors which allow direct selection for gene replacement in gram-negative bacteria. , 1993, Gene.
[25] Herbert M. Sauro,et al. In-Fusion BioBrick assembly and re-engineering , 2010, Nucleic acids research.
[26] A. Bergerat,et al. Preferential site-specific hemimethylation of GATC sites in pBR322 DNA by Dam methyltransferase from Escherichia coli. , 1989, The Journal of biological chemistry.
[27] R. Symons,et al. Biochemical method for inserting new genetic information into DNA of Simian Virus 40: circular SV40 DNA molecules containing lambda phage genes and the galactose operon of Escherichia coli. , 1972, Proceedings of the National Academy of Sciences of the United States of America.
[28] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .