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Education & Resources

Microscopy Seminars & Workshops

ibiology image

iBioseminars on Microscopy Topics

iBioseminars on microscopy Topics

Fluorescence Microscopy 

Optical Sectioning & Confocal Microscopy

Bioimage Analysis Course

 

 

Jump to: Microscopy Training Websites Resources

Microscopy Training Websites

Carl Zeiss Microscopy Online Campus

 

Carl Zeiss Microscopy Online Campus  

Olympus Tutorials

 

Olympus Tutorials

Nikon Microscopy U

Main Page    Spectral Profiles    Tutorials Resolution    Basics

adding a fluorophore

(fluorophore selection to predict and prevent crosstalk)

(A) Adding a fluorophore—press the Add fluorophore button and begin typing the name of the fluorophore. Continue to type in the name of the dye or probe to shorten the list or scroll through the list that is displayed. After a dye or probe is selected it is displayed on the plot. Selecting the Ex (excitation), Em (emission) and Display on plot to the right allows the ability to control which spectra data to remove or display on the plot. The number of Fluorophores added to the SpectraViewer will be displayed by a number located to the left of Fluorophores.

 

(B) Additional fluorophores—continue to select additional fluorophores by using the Add fluorophore at the bottom of the right-hand column.

Thermo Fisher SpectraViewer Guide (Fluorophore Selection) 

 

Nikon tutorial

(NIS Elements tutorials and basic microscopy-must request access)

Nikon E-Learning Site

 

Aliasing Plot

     

Huygens Scientific Volume Imaging

(Determine Optimal Sampling)

Resources

Teledyne Technote-Microscope
& Camera Resolution
HANDBOOK OF BIOLOGICAL
CONFOCAL MICROSCOPY
BASIC STEREOLOGY FOR BIOLOGISTS
& NEUROSCIENTISTS
Analyzing Fluorescence Microscopy
Images with ImageJ
Merge and Align
Channels using ImageJ
Overlay by Changing
Opacity using ImageJ
 

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