A New Approach to 3-Dimensional Super-Resolution Microscopy
| dc.contributor.advisor | Vaughan, Joshua | |
| dc.contributor.author | Howard, Marco d | |
| dc.date.accessioned | 2020-02-04T19:25:06Z | |
| dc.date.available | 2020-02-04T19:25:06Z | |
| dc.date.issued | 2020-02-04 | |
| dc.date.submitted | 2019 | |
| dc.description | Thesis (Ph.D.)--University of Washington, 2019 | |
| dc.description.abstract | Super-Resolution microscopy has transformed our ability to image biological specimens at the nanoscale with high contrast and molecular specificity. However, acquiring 3-dimensional images over large volumes remains a challenge because the imaging process causes fluorophores outside the focal volume to photobleach before they can be imaged. Additionally, acquiring highly multiplexed images is challenging due to a lack of spectrally distinct fluorophores which possess the required photophysical properties for super-resolution imaging. Here I present my work which specifically addresses these issues. In chapter 2 I first discuss the importance of sample preparation for super-resolution imaging. In chapter 3 I introduce a novel labeling scheme called probe-refresh STORM (prSTORM) which enables practitioners obtain multiplexed, extended-depth super-resolution images with a single dye, and in chapter 4 I show the importance of hardware for super-resolution microscopy | |
| dc.embargo.terms | Open Access | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.other | Howard_washington_0250E_21003.pdf | |
| dc.identifier.uri | http://hdl.handle.net/1773/45139 | |
| dc.language.iso | en_US | |
| dc.rights | CC BY | |
| dc.subject | DNA-Barcode | |
| dc.subject | Imaging | |
| dc.subject | Immunofluorescence | |
| dc.subject | Microscopy | |
| dc.subject | Nanoscopy | |
| dc.subject | Super-Resolution | |
| dc.subject | Bioengineering | |
| dc.subject.other | Chemistry | |
| dc.title | A New Approach to 3-Dimensional Super-Resolution Microscopy | |
| dc.type | Thesis |
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