Skip to main content
Back to Top
Augusta University Logo

Information for:

  • Current Students
  • Alumni
  • Community
  • Faculty & Staff
  • 伟德betvicror
  • Patients

Resources

  • 伟德APP
  • Calendar
  • 伟德1946英国
  • D2L LMS
  • Email
  • 伟德1946客户端下载
  • MyAugusta
  • News
  • 伟德1946娱乐城
  • Portals
  • Pounce
  • 伟德1946网页版
  • Admissions
  • 伟德1946亚洲娱乐城
  • About
  • Student Life
  • Athletics
  • Research
  • Health
  • Giving
Medical College of Georgia Neuroscience & Regenerative Medicine
Neuroscience & Regenerative Medicine
  • People
    • About the Chair
    • Faculty
      • Faculty
      • Research Scientists
    • Fellows
    • Administration
  • Education & Seminars
    • Programs
      • BS in Neuroscience (COSM)
      • MD/PhD Program
      • PhD in Neuroscience
    • Seminars
      • 2021-2022
      • 2022-2023
      • 2023-2024
      • 2024-2025
      • 2025-2026
  • PhD in Neuroscience
  • DNRM Facilities
  • Faculty Positions
  • News & Events
Education and resources promo image
  • Augusta University
  • Colleges & Schools
  • Medical College of Georgia
  • Neuroscience & Regenerative Medicine
  • Education & Resources

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 WebsitesResources

Microscopy Training Websites

Carl Zeiss Microscopy Online Campus

Carl Zeiss Microscopy Online Campus

Olympus Tutorials

Olympus Tutorials

Nikon Microscopy U

Main PageSpectral ProfilesTutorialsResolutionBasics

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

Great Doctors, Great Medicine Since 1828.

University Shield

Augusta University

1120 15th Street, Augusta, GA 30912

  • Campus Maps
  • Campus Contacts
  • 伟德APP
  • Degrees & Programs
  • Employment
  • Accessibility
  • Accreditation
  • Campus Safety
  • Compliance Hotline
  • Human Trafficking Notice
  • Privacy Notices
  • Title IX / Sexual Misconduct
伟德1946手机版 Give Now

©2025 Augusta University

Facebook Twitter LinkedIn Youtube Instagram
©
Baidu
map