Fluorescence correlation spectroscopy (FCS) can be used to investigate the photobleaching properties of fluorophores in solution. The advantage with this method is that in addition to the photobleaching rate the formation and decay rates of the triplet state can be measured. In this way, it is possible to calculate the photodestruction quantum yield and relate…
Bioimaging Template
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About the Bioimaging format
Bioimaging is a peer-reviewed journal published by Wiley, covering Advanced Fluorescence Microscopy Techniques, Photoacoustic and Ultrasonic Imaging, Cell Image Analysis Techniques.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Bioimaging 12 (3): 45–58.
Formats any DOI in Bioimaging style. No sign-up. |
| Publishes research in | Advanced Fluorescence Microscopy Techniques Photoacoustic and Ultrasonic Imaging Cell Image Analysis Techniques Optical Imaging and Spectroscopy Techniques Image Processing Techniques and Applications |
| ISSN | 0966-9051 |
| h-index | 34 |
| i10-index | 119 |
| Total citations | 4,229 |
| Top institutions publishing here | Delft University of Technology |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Bioimaging per year
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Most-cited papers in Bioimaging
Nonlinear excitation of fluorophores through molecular absorption of two or three near-infra-red photons from the tightly focused femtosecond pulses of a mode-locked laser offers the cellular biologist an unprecedented panoply of biomolecular indicators for microscopic imaging and cellular analysis. Measurements of the two-photon excitation spectra of 25 ultra-violet and visible absorbing fluorophores from 690 to…
We have developed a high sensitivity time-resolved two-photon scanning microscope. At an excitation wavelength of 960 nm, a spatial point spread function of 0.3 μm (FWHM) radially and 0.9 μm (FWHM) axially is measured for an 1.25 N.A. objective. The light source is a mode-locked titanium-sapphire laser. The time resolution is 400 ps with common…
We have developed a high sensitivity time-resolved two-photon scanning microscope. At an excitation wavelength of 960 nm, a spatial point spread function of 0.3 μm (FWHM) radially and 0.9 μm (FWHM) axially is measured for an 1.25 N.A. objective. The light source is a mode-locked titanium-sapphire laser. The time resolution is 400 ps with common…