Movie Cell-Nucleus_stack.avi Confocal Laser Scanning Microscpy image stack of a Chironomus tentans...
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Movie Cell- Nucleus_stack.avi Confocal Laser Scanning Microscpy image stack of a Chironomus tentans salivary gland cell nucleus. The fluorescence was due to the protein hrp36 conjugated to red-fluorescent AlexaFluor647, which was microinjected into the cytoplasm. After transport into the nucleus, hpr36 was incorporated into nascent RNA-particles, such that active transcription sites were marked. The brighter oval region in the image center is the cell nucleus. The polytene chromosomes showed their characteristic banding pattern. The images were aquired 15 min after after microinjection. Complete cell in fluorescence color- coded by the look-up-table „red hot“ of ImageJ Each image comprises 772x512 pixels, a total volume of 185 µm x 29 µm x 46 µm was imaged using a C- Apochromat 40X (NA 1.2 , water immersion) objective lens. The pinhole was set to 1.2 Airy units. Excitation 633nm (5% output); main dichromat UV/488/543/633; emission band pass filter LP650. Data courtesy of Dr. Jan Peter Siebrasse and Dr. Ulrich Kubitscheck, Institute of Physical and Theoretical Chemistry, Rheinische Friedrich-Wilhelms-Universtität Bonn, 2011 (For further information on the biological contents, please refer to: Siebrasse. J.P., T.Kaminski and U.Kubitscheck (2012) Nuclear export of single native mRNA molecules observed by light sheet fluorescence microscopy. Proc Natl Acad Sci USA 109: 9426-31)
Movie Cell-Nucleus_stack.avi Confocal Laser Scanning Microscpy image stack of a Chironomus tentans salivary gland cell nucleus. The fluorescence was due
Movie Cell-Nucleus_stack.avi Confocal Laser Scanning Microscpy
image stack of a Chironomus tentans salivary gland cell nucleus.
The fluorescence was due to the protein hrp36 conjugated to
red-fluorescent AlexaFluor647, which was microinjected into the
cytoplasm. After transport into the nucleus, hpr36 was incorporated
into nascent RNA-particles, such that active transcription sites
were marked. The brighter oval region in the image center is the
cell nucleus. The polytene chromosomes showed their characteristic
banding pattern. The images were aquired 15 min after after
microinjection. Complete cell in fluorescence color-coded by the
look-up-table red hot of ImageJ Each image comprises 772x512
pixels, a total volume of 185 m x 29 m x 46 m was imaged using a
C-Apochromat 40X (NA 1.2, water immersion) objective lens. The
pinhole was set to 1.2 Airy units. Excitation 633nm (5% output);
main dichromat UV/488/543/633; emission band pass filter LP650.
Data courtesy of Dr. Jan Peter Siebrasse and Dr. Ulrich
Kubitscheck, Institute of Physical and Theoretical Chemistry,
Rheinische Friedrich-Wilhelms-Universtitt Bonn, 2011 (For further
information on the biological contents, please refer to: Siebrasse.
J.P., T.Kaminski and U.Kubitscheck (2012) Nuclear export of single
native mRNA molecules observed by light sheet fluorescence
microscopy. Proc Natl Acad Sci USA 109: 9426-31)
Slide 2
Movie Cell_Nucleus_rotation.avi The above image stack was
processed and optimized for a 3D rotation presentation. All data
processing was done using ImageJ by Wayne Rasband, NIH (see
http://rsb.info.nih.gov/ij/).http://rsb.info.nih.gov/ij/ Data
courtesy of Dr. Jan Peter Siebrasse and Dr. Ulrich Kubitscheck,
Institute of Physical and Theoretical Chemistry, Rheinische
Friedrich- Wilhelms-Universtitt Bonn, 2011 (For further information
on the biological contents, please refer to: Siebrasse. J.P.,
T.Kaminski and U.Kubitscheck. 2012. Nuclear export of single native
mRNA molecules observed by light sheet fluorescence microscopy.
Proc Natl Acad Sci USA 109: 9426-31)
Slide 3
Movie Confocal_PSF.mp4 Confocal Point-Spread-Function
Calculated isointensity surfaces of the three-dimensional confocal
point- spread-function are shown for a 0.7 NA objective with a 1 AU
pinhole. The integrated intensity of the confocal psf is projected
onto the individual axes and colored according to the color bar on
the right. The isointensity surface shows all values of the psf
having the same intensity relative to the maximum of the psf and is
plotted using the same color table. We gratefully acknowledge
Nicolai Hartmann, Department of Chemistry and Center for
Nanoscience (CeNS), Ludwig-Maximilians-University Munich, for
producing this movie.
Slide 4
Movie PSF_Pinhole.mp4 Confocal Point Spread Function as a
function of Pinhole size This video shows how the confocal point
spread functions (psf) changes as the size of the pinhole is
varied. The excitation psf without pinhole is shown in the upper
left panel and the total psf is shown in the right upper panel. The
fraction of light that is transmitted through the pinhole is shown
on the graph in the lower panel with the green cursor marking the
current pinhole size for the calculated psf. The smaller the
pinhole size yields a higher overall resolution but at a
significant loss in detection yield. The lower panel shows that a
pinhole with the size of approximately 0.8 1 AU is the optimal
compromise between resolution and detection yield. We thank Achim
Hartschuh, Physical Chemistry, Department of Chemistry and Center
for Nanoscience (CeNS), Ludwig-Maximilians- University of Munich,
Germany, for producing this movie.
Slide 5
Movie Confocal_GFP_Cell.mov Confocal Image of a Huh7 cell with
eGFP-a-tubulin. This movie shows a three-dimensional reconstruction
of a z-stack of confocal images from a Huh7 cell, where a- tubulin
has been tagged with eGFP. The microtubules are clearly visible,
demonstrating the capability of confocal microscopy for three-
dimensional imaging. The diameter of the cell is approximately 60
m. Dr. Ralf Bausinger, Department of Chemistry, University of
Konstanz, Germany, is gratefully acknowledged for collecting and
processing the data and for making this video available to us.
Slide 6
Movie Single_Molecules Single DiI molecules diffusing in a
fluid glass-supported lipid bilayer. The bilayer was prepared by
vesicle-fusion from the lipid dioleyl- phosphatidylcholine (DOPC)
with low amounts of the lipohilic dye DiI (molar fraction of ~10 -8
). The detail has a size of 30 x 30 m 2, recording rate was 20
frames per second, the movie plays at real-time. Data Courtesy by
E. Klotzsch and G.J.Schtz, Institute of Applied Physics, Vienna
University of Technology, Austria