Search results

Search for "pUC19 plasmid" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays

  • Marco Russo,
  • Daniele La Corte,
  • Annalisa Pisciotta,
  • Serena Riela,
  • Rosa Alduina and
  • Paolo Lo Meo

Beilstein J. Org. Chem. 2017, 13, 2751–2763, doi:10.3762/bjoc.13.271

Graphical Abstract
  • calcium chloride in the preparation of competent cells pointless. Conclusion The binding abilities of AmCDs as bimodal supramolecular ligands were successfully tested towards neutral and anionic p-nitroaniline derivatives, sodium alginate and the pUC19 plasmid DNA, chosen as suitable models. First
PDF
Album
Supp Info
Full Research Paper
Published 18 Dec 2017

Synthesis, characterization and DNA interaction studies of new triptycene derivatives

  • Sourav Chakraborty,
  • Snehasish Mondal,
  • Rina Kumari,
  • Sourav Bhowmick,
  • Prolay Das and
  • Neeladri Das

Beilstein J. Org. Chem. 2014, 10, 1290–1298, doi:10.3762/bjoc.10.130

Graphical Abstract
  • ; ethynyl; pUC19 plasmid; triptycene tripod; Introduction Triptycene is the simplest member of the class of compounds called iptycenes. Structurally, iptycenes have a number of arene rings joined together to form the bridges of [2.2.2]bicyclic ring systems. In triptycene, the bicyclic ring is decorated
  • spectrum of the product 7 and 8 between 8.9–9.1 ppm confirms the formation of triphosphines. Biological studies: Interaction of triptycene derivatives with DNA All the triptycene derivatives, when incubated with plasmid DNA show different degree of nuclease activity on supercoiled pUC19 plasmid DNA. The
  • : pUC19 plasmid, Uracil DNA Glycosylase (UDG) enzyme, APE1 enzyme, BamHI, and HindIII restriction endonucleases were purchased from New England Biolabs (USA). HPLC-purified monouracil-containing synthetic deoxyoligomers were purchased from Sigma-Aldrich and deoxyoligomer concentrations were adjusted as
PDF
Album
Supp Info
Full Research Paper
Published 05 Jun 2014
Other Beilstein-Institut Open Science Activities