Subject |
Nanotechnology |
Specific subject area |
Super-resolution microscopy |
Type of data |
Time-lapse records |
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Lists of single-molecule localization space-time coordinates |
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Matlab functions |
How data were acquired |
Total internal reflection fluorescence microscope |
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Instrument: Nikon N-STORM microscope. |
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Softwares: NIS-elements (Nikon) |
Data format |
Raw |
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analyzed |
Parameters for data collection |
Particles on glass coverslip were imaged with continuous laser excitation (647 nm) under total internal reflection conditions. Fluorescence time-lapse records of 10,000–50,000 frames were acquired at 10–20 Hz onto a region of the camera of 40 µm in size. |
Description of data collection |
Binding sites exposed on streptavidin-coated polystyrene particles were loaded with biotin-conjugated short single strands of DNA and seeded on glass coverslip. A complementary free single strand of DNA, conjugated with a fluorophore, was introduced at low concentration (0.1 – 5 nM) in solution and time-lapse fluorescence imaging acquisitions were recorded. |
Data source location |
Institution: Institute for Bioengineering of Catalonia (IBEC) |
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City: Barcelona |
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Country: Spain |
Data accessibility |
In a public repository |
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Repository name: 4TU-center for Research Data |
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Data identification number: uuid:50bd0ad4-52d8-4138-8eb1-40b4d7fc2286 |
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Direct URL to data: https://doi.org/10.4121/uuid:50bd0ad4-52d8-4138-8eb1-40b4d7fc2286
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Related research article |
Delcanale et al., Nanoscale Mapping Functional Sites on Nanoparticles by Points Accumulation for Imaging in Nanoscale Topography (PAINT), ACS Nano, 10.1021/acsnano.7b09063 [1]
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