Confocal microscope images show far fewer horizontal cells generated in mice without Onecut1 (bottom panels) compared to those in normal mice (top panels).
Not exact matches
The Shot: Pan took this digital
image with an Olympus FluoView FV1000
confocal microscope using a 20x objective and a photomultiplier tube.
This
image was created using a laser scanning
confocal microscope by Igor Siwanowicz of Howard Hughes Medical Institute.
This an
image taken of a toroid using a
confocal microscope, false - colored by height.
Companies making high - content cell imaging equipment such as
confocal microscopes and plate readers are now adding software tools to process
images of 3D cell cultures.
In their new study, they adapted DNA - PAINT technology to
microscopes that are widespread among cell biology laboratories, called
confocal microscopes, and that are used by researchers to
image whole cells and thicker tissues at lower resolution.
In addition to fruit flies, they successfully used the program to analyze
images of zebrafish and mice, as well as data collected from a commercial light sheet
microscope and a commercial
confocal microscope.
Z - stack
images of taste buds and geniculate ganglia were collected on an Olympus Fluoview FV300 laser scanning
confocal microscope with a 60 × oil - immersion objective [numerical aperture (NA) 1.3] and 20 × oil - immersion objective (NA 0.7) or on a Leica TCS SP5 laser scanning
confocal microscope with a 63 × oil - immersion objective (NA 1.4).
The CARS
images were acquired with a Leica TCS SP8 CARS system (Leica Microsystems, Mannheim, Germany) consisting of a TCS SP8
confocal microscope combined with a picoEmerald laser (APE, Berlin, Germany) offering a fixed Stokes laser line of 1064.5 nm and a tuneable Pump line from an optical parametric oscillator (780 nm — 940 nm).
Cultured Aplysia neurons are
imaged by post-doctoral scientist Joseph Rayman on Kavli Columbia's
confocal laser scanning
microscope.
A
microscope and its parts,
image formation, Köhler illumination, optical aberrations, types of lenses, phase contrast, interference contrast, polarization, fluorescence microscopy, laser
confocal microscopy, two - photon
confocal microscopy, superresolution microscopy, study of dynamic processes in living cells, immunofluorescence.
Images were acquired with a LSM710 Zeiss
confocal laser scanning system or Olympus IX81 light
microscope.
Images were taken with the
confocal microscopes Zeiss LSM710 and
image analysis was accomplished with Fiji (ImageJ).
The
image was taken with a
confocal laser scanning
microscope and shows cells giving strong inmmunofluorescence staining for CD3 antigen (green), indicating presence of cells of T - lymphocytes origin in the infarct zone of the heart tissue, counterstained nuclei with DAPI (blue).
Images were taken on a Zeiss LSM 510
confocal microscope (Carl Zeiss, Canada) equipped with Argon and Helium - Neon lasers.
Unlike laser scanning
confocal microscopes (LSM) which scan one point of laser light across an entire field, a spinning disk
confocal scans approximately 1,000 points of laser light across the field simultaneously resulting in much faster
image production.
Fluorescence
images were acquired using a LSM700
confocal microscope (Zeiss).
Labeled sections were examined and
imaged using a Zeiss 510 Meta
confocal microscope.
Imaged with a Zeiss LSM780
confocal microscope.
There, she managed a large number of
confocal, advanced light, transmission, and scanning electron
microscopes, as well as
image processing and bioinformatics.
Specimens were
imaged using a Zeiss Meta 510
confocal microscope maintaining the same imaging settings for each set of experiments.
Confocal images were obtained with a Leica SPE or an Olympus FV 1000
microscope.
Point scanning
confocal and 2 - photon
microscopes which rely on building an entire
image pixel by pixel are unable to provide the frame - rates necessary for imaging tissues of this size.
Slides were washed, counterstained with 4 ′, 6 - diamidino -2-phenylindole (DAPI), mounted in fluorescent mounting media (DAKO), and
imaged using a Nikon Eclipse TE2000 - U
microscope equipped with a SPOT RT Slider digital camera or
confocal imaging using a Zeiss LSM 510
confocal microscope (Carl Zeiss Microimaging).
Slides were
imaged using a
confocal laser scanning
microscope (LSM 700, Zeiss).
Images were obtained using a Zeiss
confocal microscope with Nomarski optics and analysed with LSM
Image Browser software.
This
image from a
confocal microscope shows neural stem cells (green) in the mouse hippocampus that are actively proliferating because they express Ki67 (red), a protein that is only present in proliferating cells.
The
microscope and its components,
image formation, microscopy in both transmitted and fluorescent light, Kohler illumination, optical aberrations, objective lens types, phase contrast, interference contrast, polarization, fluorescence microscopy, laser
confocal microscopy, two - photon
confocal microscopy, super-resolution microscopy, study of dynamic processes in living cells, immunofluorescence.
Our modern imaging center is equipped with state - of - the - art
confocal laser scanning
microscopes, fluorescence and stereo
microscopes, two photon
microscope, laser microdissection
microscope and powerful
image analysis computers with imaging software.