Introducing Aplo Scope: A new era in super-resolution imaging! learn more >
Biorxiv, September 2020
Tamara Madácsy, Árpad Varga, Noémi Papp, Barnabás Deák, Bálint Tél, Petra Pallagi, Viktória Szabó, Júlia Fanczal, Zoltan Rakonczay Jr., Zsolt Rázga, Meike Hohwieler, Alexander Kleger, Mike Gray, Péter Hegyi, József Maléth
PNAS, May 2021
M. T. Gyparaki, A. Arab, E. M. Sorokina, A. N. Santiago-Ruiz, C. H. Bohrer, J. Xiao, M. Lakadamyali,
University of Pennsylvania orthopaedic journal , June 2020
Lab on a Chip, October 2020
Yigang Shen, Yaxiaer Yalikun, Yusufu Aishan, Nobuyuki Tanaka, Asako Satob and Yo Tanaka
The Journal of Immunology, May 2020
Sheila Burns and Michael Senior
Cells, July 2020
Katharina Grikscheit, Olga Dolnik, Yuki Takamatsu, Ana Raquel Pereira and Stephan Becker
We have put together some tips to help you optimize your immunofluorescence staining protocol and increase the signal-to-noise ratio in your samples.
When preparing a sample for STORM microscopy it is also crucial to select an appropriate buffer solution, which will efficiently regulate blinking behavior and help achieve high quality super-resolution images. Here is a brief guide to STORM buffer components and how they can affect sample imaging.
We've put together a one page, printable PDF to help you choose between the Nanoimager's key super-resolution microscopy techniques. It covers core techniques including dSTORM, PALM, SPT and smFRET.
