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Grant: Research Tools and Instruments - Category 1 (<$150,000)

University of Windsor

$131,000.00

Confocal microscope for multichannel and live imaging

FY 2007-08

Summary
Cell Biology has been revolutionized by the development of fluorescent probes that can be used to track the localization of proteins in living cells.  The increasing variety of fluorescent probes with different spectral characteristics has allowed their use in colocalization studies involving mutiple cell components.  A major limitation with traditional fluorescent microscopy is in the difficulty of observing structures deep within thick specimens.  The advent of confocal microscopy has lead to a second revolution in imaging in biology.  The confocal microscope scans the sample using a beam of laser light that is focused only on the plane of interest.  This allows filtering out of signal coming from out-of-focus areas of the sample, and has opened up the exciting possibility of viewing proteins in the context of their native tissue or even in whole organisms.  In an increasing number of cases the simultaneous acquisition of data for 3 or more different proteins is required to determine where a protein resides and its relation to other proteins or structures in the cell.  Recently, the ability to observe proteins in living cells or whole organisms has once more revolutionized cell biology by allowing researchers to study cellular processes in real time.  The newer generation of confocal microscopes offer fast scanning speeds that make live imaging feasable.  Our investigator group is currently utilizing multiple fluorescent probes to study a wide variety of biological processes.  However, we are limited by lack of access to an operable confocal microscope.  The existing confocal microscoope in the Department is not made for live imaging.  It is also limited in the number of proteins that can be detected.  Furthermore, it is from a company that no longer makes or services confocals.  It is costly to maintain and it is not possible to replace or upgrade the aging components.  There is no other confocal microscope on campus or in the city.  We are asking for a new confocal that will be able to perform at the level demanded by our research needs.  This equipment will allow us to continue to train quality scientists and maintain an excellent research program.
Program
Research Tools and Instruments - Category 1 (<$150,000)
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
345929-2007
Name nom
Swan, Andrew
Department département
Biological Sciences
Organization id
37
Institution établissement
University of Windsor
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2007
Award amount
131000
Program id
EQPEQ
Program name en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
33
Committee name en
Molec. & Develop. Genetics
Committee name fr
Gén. moléculaire et dévelop.
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
1
Nb partie
1
Application title
Confocal microscope for multichannel and live imaging
Keyword
NA
Application summary
Cell Biology has been revolutionized by the development of fluorescent probes that can be used to track the localization of proteins in living cells.  The increasing variety of fluorescent probes with different spectral characteristics has allowed their use in colocalization studies involving mutiple cell components.  A major limitation with traditional fluorescent microscopy is in the difficulty of observing structures deep within thick specimens.  The advent of confocal microscopy has lead to a second revolution in imaging in biology.  The confocal microscope scans the sample using a beam of laser light that is focused only on the plane of interest.  This allows filtering out of signal coming from out-of-focus areas of the sample, and has opened up the exciting possibility of viewing proteins in the context of their native tissue or even in whole organisms.  In an increasing number of cases the simultaneous acquisition of data for 3 or more different proteins is required to determine where a protein resides and its relation to other proteins or structures in the cell.  Recently, the ability to observe proteins in living cells or whole organisms has once more revolutionized cell biology by allowing researchers to study cellular processes in real time.  The newer generation of confocal microscopes offer fast scanning speeds that make live imaging feasable.  Our investigator group is currently utilizing multiple fluorescent probes to study a wide variety of biological processes.  However, we are limited by lack of access to an operable confocal microscope.  The existing confocal microscoope in the Department is not made for live imaging.  It is also limited in the number of proteins that can be detected.  Furthermore, it is from a company that no longer makes or services confocals.  It is costly to maintain and it is not possible to replace or upgrade the aging components.  There is no other confocal microscope on campus or in the city.  We are asking for a new confocal that will be able to perform at the level demanded by our research needs.  This equipment will allow us to continue to train quality scientists and maintain an excellent research program.