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High-Contrast Visualization of Endogenous Proteins for Live Imaging

Published online by Cambridge University Press:  05 August 2019

Dale A. Fortin
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
Joshua B. Melander
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
Bart C. Jongbloets
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
Wei-Hong Xiong
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
Caiying Guo
Affiliation:
Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, VA, USA.
Tianyi Mao
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
Haining Zhong*
Affiliation:
Vollum Institute, Oregon Health & Science University, Portland, OR, USA.
*
*Corresponding author: [email protected]

Abstract

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Type
Light and Fluorescence Microscopy for Imaging Cell Surface and Cell Structure
Copyright
Copyright © Microscopy Society of America 2019 

Footnotes

3

Present address: Stanford Neurosciences Program, Stanford University, Stanford, CA, USA.

References

[1]Chalfie, M et al. , Science 263 (1994), p. 802.Google Scholar
[2]Cubitt, AB et al. , Trends Biochem Sci 20(11) (1995), p. 448.Google Scholar
[3]Kim, E and Sheng, M, Nat Rev Neurosci 5(10) (2004), p. 771.Google Scholar
[4]El-Husseini, AE et al. , Science 290(5495) (2000), p. 1364.Google Scholar
[5]Stein, V et al. , J Neurosci 23(13) (2002), p. 5503.Google Scholar
[6]Fortin, DA et al. , J Neurosci 34(50) (2014), p. 16698.Google Scholar
[7]This work was supported by NIH grants to HZ (DP2OD008425, R21NS084315, and R21NS097856) and TM (R01NS081071) and by HHMI.Google Scholar