K
Krishna N. Ganesh
Researcher at National Chemical Laboratory
Publications - 114
Citations - 2693
Krishna N. Ganesh is an academic researcher from National Chemical Laboratory. The author has contributed to research in topics: DNA & Oligonucleotide. The author has an hindex of 28, co-authored 106 publications receiving 2584 citations. Previous affiliations of Krishna N. Ganesh include Indian Institute of Chemical Technology.
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Electrostatic Assembly of Nanoparticles and Biomacromolecules
TL;DR: This Account deals with assembling surface-modified nanoparticles in thin film form using electrostatic interactions at the air-water interface and in thermally evaporated lipid films.
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Isothermal Titration Calorimetry Studies on the Binding of Amino Acids to Gold Nanoparticles
TL;DR: ITC may be used to follow the binding of ligands such as amino acids to the surface of inorganic materials such as gold nanoparticles as well as other techniques such as gel electrophoresis and X-ray photoemission spectroscopy.
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Linear Superclusters of Colloidal Gold Particles by Electrostatic Assembly on DNA Templates
Ashok Kumar,Mrunalini Pattarkine,Mohan M. Bhadbhade,A.B. Mandale,Krishna N. Ganesh,Suwarna Datar,C. V. Dharmadhikari,Murali Sastry +7 more
TL;DR: In this article, the Coulombic interaction between positively charged amine groups on gold particle surfaces and negatively charged phosphate backbones of DNA molecules drives the self-assembly of gold nanoparticles into linear supercluster structures.
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Isothermal Titration Calorimetry Studies on the Binding of DNA Bases and PNA Base Monomers to Gold Nanoparticles
TL;DR: An isothermal titration calorimetric investigation of the interaction of DNA bases and PNA base monomers with gold nanoparticles is described revealing a binding sequence in the order C > G > A > T.
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Taxol-DNA interactions: fluorescence and CD studies of DNA groove binding properties of taxol.
TL;DR: Using fluorescence spectroscopy, it is shown that taxol binds to DNA with an affinity constant of 1.08 x 10(7) M-1, accompanied by a large 'red edge excitation shift' of fluorescence emission maximum in taxol-DNA complex.