Skip to main content Accessibility help
×
Home

Freeze Drying Method with Gaseous Nitrogen to Preserve Fine Ultrastructure of Biological Organizations for Scanning Electron Microscopy, Helium Ion Beam Microscopy and Fluorescence Microscopy

  • Kunihiro Uryu (a1), Nadine Soplop (a1), Devrim Acehan (a1), Benjamin Y. Winer (a2), Vincent A. Fischetti (a2), Timothy Sheahan (a3), Charles M. Rice (a3), Mayla Hsu (a4), Melissa Robbiani (a4), Gaetano Santulli (a5), Hana Totary-Jain (a5) (a6), Bernhard Goetze (a7) and Maria-Teresa Catanese (a3) (a8)...
    • Send article to Kindle

      To send this article to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

      Note you can select to send to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

      Find out more about the Kindle Personal Document Service.

      Freeze Drying Method with Gaseous Nitrogen to Preserve Fine Ultrastructure of Biological Organizations for Scanning Electron Microscopy, Helium Ion Beam Microscopy and Fluorescence Microscopy
      Available formats
      ×

      Send article to Dropbox

      To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

      Freeze Drying Method with Gaseous Nitrogen to Preserve Fine Ultrastructure of Biological Organizations for Scanning Electron Microscopy, Helium Ion Beam Microscopy and Fluorescence Microscopy
      Available formats
      ×

      Send article to Google Drive

      To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

      Freeze Drying Method with Gaseous Nitrogen to Preserve Fine Ultrastructure of Biological Organizations for Scanning Electron Microscopy, Helium Ion Beam Microscopy and Fluorescence Microscopy
      Available formats
      ×

Abstract

Copyright

References

Hide All
[1] Hart, GW & Copeland, RJ Cell 143 (2010). p 672.
[2] Krueger, CM, Neufeld, EJ & Saffitz, JE J Histochem Cytochem 33 (1985). p 799.
[3] Ongun, A, Thomson, WW & Mudd, JB J Lipid Res 9 (1968). p 416.
[4] Saunders, DR, Wilson, J & Rubin, CE J. Cell Biol. 37 (1968). p 183.
[5] Dallam, RD J Histochem Cytochem 5 (1987). p 178.
[6] Joens, MS, Huynh, C, Kasuboski, JK, et al., Sci. Rep 3 (2013). p 3514.
[7] Acknowledgements: The current study was supported by The Rockefeller University, the American Heart Association Scientist Developmental Grant 15SDG25300007 (Santulli), the United States Agency for International Development Cooperative Agreement GPO-A-00-04-00019-00 (Robbiani), the NIH grant AI098645 (Robbiani), the TNPRC NIH base grant P51 OD011104-52 (Robbiani), NIH R01 AI072613 (Rice), NIH R01 CA057973 (Rice), NHLBI/NIH R00HL109133 (Totary-Jain) and ContraFect Corporation (Fischetti).

Metrics

Full text views

Total number of HTML views: 0
Total number of PDF views: 0 *
Loading metrics...

Abstract views

Total abstract views: 0 *
Loading metrics...

* Views captured on Cambridge Core between <date>. This data will be updated every 24 hours.

Usage data cannot currently be displayed