• Jump to Content
Scientific Volume Imaging
Error CapsLock is on.
I forgot my password.
Register
  • Home
  • News
    • Announcements
    • Conferences and Workshops
    • Projects
  • Products
    • Huygens Specifications
    • Huygens Essential
    • Huygens Professional
    • Huygens Scripting
    • Huygens Core
    • Deconvolution and Restoration Options
    • Functional Options
    • Visualization Options
    • Analysis Options
    • Server Options and Available Platforms
    • What's New
  • Solutions
    • Training
    • Classroom License
    • Remote Display
    • Imaging Service
  • Gallery
    • Movie Gallery 1
    • Movie Gallery 2
    • Movie Gallery 3
    • Image Gallery 1
    • Image Gallery 2
    • Image Gallery 3
    • Screenshots
  • Download
    • Software
    • Manuals
    • Presentations
    • Demo Images
  • Support
    • Search
    • Support Wiki
    • Documentation
    • Frequently Asked Questions
    • Software Installation
    • Trial License
    • Request Support
    • Nyquist Calculator
    • Backprojected Pinhole Calculator
  • About SVI
    • About the Company
    • Contact Details
    • Job Openings
    • Staff
    • Trainees
  • FAQ
  • Trial License
  • Request Quote
Print
  • Left
    • AiryDisk BackGround BackProjected BackProjectedPinholeRadius BleachingMode BlurAndNoiseAffectColocalization ConvolvingTrains DeconvolutionForNonOpticalImages FluorescenceMicroscope FourPiMicroscope HuygensEssential MicroscopicParameters MismatchDistortsPsf MismatchInRecordedBeads NipkowDiskMicroscope NumberOfPsfSlices NyquistCalculator PinholeAndBandwidth PinholeAndResolution PinholeRadius SamplingDensity SamplingDensityZImpFaq SamplingRate SamplingRates SlitScanner TheoVsExpPsf ThreeDeeMicroscope WideFieldMicroscope

Confocal microscope


A Confocal microscope is one type of 3D Fluorescence Microscope in which resolution is increased by rejecting out-of-focus light. This is done by using pinholes with special Pinhole Radius and makes it to be an intrinsic 3D microscope: due to the focusing nature of the confocal microscope, it is specially suitable for obtaining 3D images as a collection of intensities at different points of the space.

A recommendable accessible explanation of how a confocal microscope works: http://www.physics.emory.edu/~weeks/confocal/

In confocal microscopes, the →Nyquist Rate is about one half of that in Wide Field Microscopes.


Page Title Search

Menu

  • Home Page
  • Support Wiki
  • Documentation
  • Software Installation
  • Request Support
  • Nyquist Calculator
  • Backprojected Pinhole Calculator
  • Disclaimer
  • About This Wiki

Last Visits

  • ConfocalMicroscope
  • ColocalizationCoefficients
  • ColocalizationBasics
  • CoLocalization
  • ClassicMaximumLikelihoodEstimation

Follow us

Follow @svi_huygens

Headlines

  • STED deconvolution now available in Huygens (Thu 23 of Feb., 2012)
  • Migration of a Huygens license allowed every M&U year (Fri 06 of Jan., 2012)
  • Huygens Image Contest 2011 (Wed 14 of Dec, 2011)
  • Huygens Remote Manager 2.1 released (Tue 06 of Dec, 2011)
  • Huygens Essential 4.1 version available! (Tue 15 of Nov., 2011)
  • RBNCC for Colocalization Analyzer now available (Tue 11 of Oct., 2011)
  • Huygens participates in Nanoscopy science project (Sun 29 of May, 2011)

Upcoming Events

1)  Tue 05 of June, 2012
SVI Team present at ELMI conference in Leuven Belgium
2)  Thu 20 of Sep., 2012
Huygens Course September 20 until 22 of September 2012, Hilversum, NL

Contact Information

Scientific Volume Imaging B.V.

Laapersveld 63
1213 VB Hilversum
The Netherlands
(external link)

Phone: +31 (0)35 64216 26
E-mail: info at svi.nl

Mobile

Switch to mobile site

Copyright 1995-2012 Scientific Volume Imaging B.V. - Images used with permission.
Powered by Tiki Wiki CMS Groupware | Theme: BusinessSVIRed
Feed Wiki