Skip to main content

Presentation of Confocal Images

  • Protocol
Confocal Microscopy Methods and Protocols

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 122))

Abstract

Confocal microscopy is routinely used to produce high-resolution images of single, double-, and triple labeled fluorescent samples. The images are collected as single optical sections (2D imaging), as Z-series (3D imaging), as time-lapse series (2D over time), or as Z-series over time (3D over time or 4D imaging). Because the images are in a digital format, they can be further manipulated using a range of software.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. White N. S. (1995) Visualization systems for multidimensional CLSM images, in Handbook of Biological Confocal Microscopy, Plenum Press, New York.

    Google Scholar 

  2. Thomas, C., DeVries, P., Hardin, J., and White, J. (1996) Four-dimensional imaging: computer visualization of 3D movements in living specimens. Science 273, 603–607.

    Article  PubMed  CAS  Google Scholar 

  3. Mohler, W. A., and White, J. G. (1998) Stereo-4-D reconstruction and animation from living fluorescent specimens. BioTechniques 24, 1006–1012.

    PubMed  CAS  Google Scholar 

  4. Schrock, E., du Manoir, S., Veldman, T., Schoell, B., Wienberg, J., Ferguson-Smith, M. A., Ning, Y., Ledbetter, D. H., Bar-Am, I., Soenksen, D., Garini, Y., Ried, T. (1996) Multicolor spectral karyotyping of human chromosomes. Science 273, 494–497.

    Article  PubMed  CAS  Google Scholar 

  5. Waggoner, A. S., DeBiasio, R., Conrad, P., Bright, G. R., Ernst, L. A., Ryan, K., Nederlof, M., Taylor, D. L. (1989) Multiple spectral parameter imaging. Methods in Cell Biol. 30, 449–478.

    Article  CAS  Google Scholar 

  6. Paddock, S. W., Langeland, J. A., DeVries, P. J., and Carroll, S. B. (1993) Three-color immunofluorescence imaging of Drosophila embryos by laser scanning confocal microscopy. BioTechniques 14, 42–48.

    PubMed  CAS  Google Scholar 

  7. Kiehart, D. P., Montague, R. A., Rickoll, W. L., Thomas, G. H., and Foard, D. (1994) High-resolution microscopic methods for the analysis of cellular movements in Drosophila embryos. Methods Cell Biol. 44, 507–532.

    Article  PubMed  CAS  Google Scholar 

  8. Paddock, S. W., DeVries, P. J., Buth, E., and Carroll, S. B. (1994) Morphing: a new graphics tool for animating confocal images. BioTechniques 16, 448–452.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1999 Humana Press Inc., Totowa, NJ

About this protocol

Cite this protocol

Halder, G., Paddock, S.W. (1999). Presentation of Confocal Images. In: Paddock, S.W. (eds) Confocal Microscopy Methods and Protocols. Methods in Molecular Biology™, vol 122. Humana Press. https://doi.org/10.1385/1-59259-722-X:373

Download citation

  • DOI: https://doi.org/10.1385/1-59259-722-X:373

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-526-3

  • Online ISBN: 978-1-59259-722-2

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics