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https://www.researchgate.net/publication/305479119_MiniTn7-transposon_delivery_vectors_for_inducible_or_constitutive_fluorescent_protein_expression_in_Enterobacteriaceae
Jul 20, 2016 · MiniTn7-transposon delivery vectors for inducible or constitutive fluorescent protein expression in Enterobacteriaceae ... delivery plasmids in combination with the conjugation strain ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972447/
The use of miniTn7-transposon delivery plasmids is widespread in molecular and environmental microbiology, e.g. to chromosomally integrate promoter-reporter gene constructs (Choi and Schweizer 2006, McKenzie and Craig 2006, Lagendijk et al. 2010) or for the complementation of knockout mutants (Crepin, Harel and Dozois 2012).Author: Mitja N. P. Remus-Emsermann, Pascal Gisler, David Drissner
http://comstat.dk/reswiki/lib/exe/fetch.php?media=tn7plasmids.pdf
Mini-Tn7 delivery plasmids, ver. 1 1 Mini-Tn7 transposons – the delivery plasmids See also the documents: “The Tn7 transposon ” and “How to use the mini-Tn7 transposons”. Note ! The delivery plasmids presented here are all pUC19 derivatives and can replicate in E. coli and other enterics, but for example not in Pseudomonas. Only characters inserted as part
https://www.researchgate.net/publication/8521456_Mini-Tn7_transposons_for_site-specific_tagging_of_bacteria_with_fluorescent_proteins
We have expanded the panel of mini-Tn7 delivery plasmids expressing different fluorescent proteins (stable and unstable) from the Escherichia coli lac derived promoter, P(A1/04/03), or from the ...
http://comstat.dk/reswiki/lib/exe/fetch.php?media=tn7howto.pdf
In addition, the plasmids contain a mob region, which can be used for mobilising the plasmid from one bacterium to another by the RP4/ RK2 transfer genes, e.g. located on the plasmid pRK600. Constructed delivery plasmids of this series are shown in the document:”Mini-Tn7 delivery plasmids”, see also Lambertsen et al., 2003. Helper plasmidFile Size: 176KB
https://apps.dtic.mil/dtic/tr/fulltext/u2/a450025.pdf
mini-Tn7 insertion in bacteria with multiple glmS-linked attTn7 sites: example Burkholderia mallei ATCC 23344 Kyoung-Hee Choi1, David DeShazer2 & Herbert P Schweizer1 1Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523-1682, USA; 2Bacteriology Division, US Army Medical Research Institute of Infectious Diseases, Fort Detrick, …Author: Kyoung-Hee Choi, David DeShazer, Herbert P Schweizer
https://www.ncbi.nlm.nih.gov/pubmed/15186351
The mini-Tn7 transposon system is a convenient tool for site-specific tagging of bacteria in which the tagging DNA is inserted at a unique and neutral chromosomal site. We have expanded the panel of mini-Tn7 delivery plasmids expressing different fluorescent proteins (stable and unstable) from the Escherichia coli lac derived promoter, P(A1/04 ...Author: Lotte Lambertsen, Claus Sternberg, Søren Molin
https://bmcresnotes.biomedcentral.com/articles/10.1186/1756-0500-5-157
Mar 20, 2012 · Development of a mini-Tn7 based ori R6Kγ chromosomal insertion system. We sought to employ the mini-Tn7 method described by McKenzie and Craig [] for chromosomal insertion of pir alleles in the absence of selection. For this purpose, the pir + and pir-116 genes were cloned into the mini-Tn7 delivery vector pGRG36 (Figure 1) and published procedures [] followed in an attempt to transpose …Author: Brian H Kvitko, Steven Bruckbauer, John Prucha, Ian McMillan, Erin J Breland, Stephanie Lehman, Kati...
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