Literature DB >> 9223680

A high-resolution, confocal laser-scanning microscope and flash photolysis system for physiological studies.

I Parker1, N Callamaras, W G Wier.   

Abstract

We describe the construction of a high-resolution confocal laser-scanning microscope, and illustrate its use for studying elementary Ca2+ signalling events in cells. An avalanche photodiode module and simple optical path provide a high efficiency system for detection of fluorescence signals, allowing use of a small confocal aperture giving near diffraction-limited spatial resolution (< 300 nm lateral and < 400 nm axial). When operated in line-scan mode, the maximum temporal resolution is 1 ms, and the associated computer software allows complete flexibility to record line-scans continuously for long (minutes) periods or to obtain any desired pixel resolution in x-y scans. An independent UV irradiation system permits simultaneous photolysis of caged compounds over either a uniform, wide field (arc lamp source) or at a tightly focussed spot (frequency-tripled Nd:YAG laser). The microscope thus provides a versatile tool for optical studies of dynamic cellular processes, as well as excellent resolution for morphological studies. The confocal scanner can be added to virtually any inverted microscope for a component cost that is only a small fraction of that of comparable commercial instruments, yet offers better performance and greater versatility.

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Year:  1997        PMID: 9223680     DOI: 10.1016/s0143-4160(97)90055-5

Source DB:  PubMed          Journal:  Cell Calcium        ISSN: 0143-4160            Impact factor:   6.817


  23 in total

1.  Buffer kinetics shape the spatiotemporal patterns of IP3-evoked Ca2+ signals.

Authors:  Sheila L Dargan; Ian Parker
Journal:  J Physiol       Date:  2003-10-10       Impact factor: 5.182

Review 2.  [Optical imaging of fluorescence in the near infrared. From passive to enzymatically activated contrast medium].

Authors:  M Funovics
Journal:  Radiologe       Date:  2007-01       Impact factor: 0.635

3.  Analysis of puff dynamics in oocytes: interdependence of puff amplitude and interpuff interval.

Authors:  Daniel Fraiman; Bernardo Pando; Sheila Dargan; Ian Parker; Silvina Ponce Dawson
Journal:  Biophys J       Date:  2006-03-13       Impact factor: 4.033

4.  Theoretical analysis of the Ca2+ spark amplitude distribution.

Authors:  L T Izu; W G Wier; C W Balke
Journal:  Biophys J       Date:  1998-09       Impact factor: 4.033

5.  Variability in frequency and characteristics of Ca2+ sparks at different release sites in rat ventricular myocytes.

Authors:  I Parker; W G Wier
Journal:  J Physiol       Date:  1997-12-01       Impact factor: 5.182

6.  A continuum of InsP3-mediated elementary Ca2+ signalling events in Xenopus oocytes.

Authors:  X P Sun; N Callamaras; J S Marchant; I Parker
Journal:  J Physiol       Date:  1998-05-15       Impact factor: 5.182

7.  Activation and co-ordination of InsP3-mediated elementary Ca2+ events during global Ca2+ signals in Xenopus oocytes.

Authors:  N Callamaras; J S Marchant; X P Sun; I Parker
Journal:  J Physiol       Date:  1998-05-15       Impact factor: 5.182

8.  Cytosolic [Ca2+] regulation of InsP3-evoked puffs.

Authors:  Michiko Yamasaki-Mann; Angelo Demuro; Ian Parker
Journal:  Biochem J       Date:  2013-01-01       Impact factor: 3.857

9.  Kinetics of elementary Ca2+ puffs evoked in Xenopus oocytes by different Ins(1,4,5)P3 receptor agonists.

Authors:  J S Marchant; I Parker
Journal:  Biochem J       Date:  1998-09-15       Impact factor: 3.857

10.  Hemispheric asymmetry of macroscopic and elementary calcium signals mediated by InsP3 in Xenopus oocytes.

Authors:  N Callamaras; X P Sun; I Ivorra; I Parker
Journal:  J Physiol       Date:  1998-09-01       Impact factor: 5.182

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