Testimonials
Magnetherm testimonials
“As a company who make magnetic nanoparticles and magnetic fluids for a diverse range of applications, we need to quantify the magnetic, rheological and structural properties of these materials. As we are now developing these exciting materials for therapeutic applications, we also need to quantify the heating properties of these particles for potential hyperthermia therapies. The nanoTherics Magnetherm device provides an affordable and user friendly solution for hyperthermia heating measurements. We have been using the device for over a year now and it has proved invalubale to us fo the design of our particles. Together with a responsive and friendly after sales service provided by nanoTherics, our user experience with the Magnetherm has been very productive.” Dr. Vijay Patel, General Manager, Liquids Research Limited, UK. www.liquidsresearch.com
magnefect testimonials
“I am very impressed with the magnefect-nano and its capabilities in transfecting primary neuronal cultures. Not only do we see better viability of the cells post-transfection compared to other commercial transfection devices we have used, but the magnefect-nano can also be used to transfect fully differentiated neurons adherent to the culture wells at various time points after plating. Retransfection of the cultures is also an option with this device. I have also thoroughly enjoyed working with the scientists at Nanotherics, where I have received full support from them while optimizing transfection procedures for primary neuronal cultures.” Dr Joseph Steiner, Associate Professor or Neurology, Johns Hopkins University, USA
“nanotherics friendly and interactive team is greatly helping us to establish the best conditions for neuronal transfection. We are very excited about the versatility of this technology that limits adverse effects on cell viability.” Dr Elena Di Daniel, Takeda, Cambridge, UK
“We have tested the magnefect-nano device in the lab for transfection of cultured Dorsal Root Ganglion neurons. The machine is easy to use and provides impressive transfection efficiency of DRG cultures (up to 15% for neurons and up to 70% for glial cells). Cell viability is also good. Overall – a good alternative to the existent methods for transfection of primary cultures.” Dr Nikita Gamper, Leeds, UK
“An efficient alternative to lipid-based siRNA delivery” Dr Gualtiero Alvisi, University of Heidelberg, Germany