Open Access. Powered by Scholars. Published by Universities.®

Digital Commons Network

Open Access. Powered by Scholars. Published by Universities.®

Biology

PDF

Utah State University

1994

Electron probe microanalysis

Articles 1 - 2 of 2

Full-Text Articles in Entire DC Network

Quantitative Dark-Field Mass Analysis Of Ultrathin Cryosections In The Field-Emission Scanning Transmission Electron Microscope, S. Brian Andrews, Roger A. Buchanan, Richard D. Leapman Apr 1994

Quantitative Dark-Field Mass Analysis Of Ultrathin Cryosections In The Field-Emission Scanning Transmission Electron Microscope, S. Brian Andrews, Roger A. Buchanan, Richard D. Leapman

Scanning Microscopy

The availability of a cryotransfer stage, highly efficient electron energy loss spectrometers, and ultrathin-window energy-dispersive x-ray spectrometers for the VG Microscopes HB501 field-emission scanning transmission electron microscope (STEM) provides this instrument with the potential for high resolution biological microanalysis. Recent technical advances offer cryosections that are thin enough to take advantage of the analytical capabilities of this microscope. This paper first discusses the quantitative characterization of freeze-dried, ultrathin cryosections of directly frozen liver and brain by low-dose dark-field STEM imaging. Such images reveal high-quality sections with good structural detail, mainly due to reduced preparation artifacts and electron beam damage. These …


Measurement Of Subcellular Ca2+ Redistribution In Cardiac Muscle In Situ: Time Resolved Rapid Freezing And Electron Probe Microanalysis, Meredith Bond, Mark D. Schluchter, Eva Keller, Christine S. Moravec Jan 1994

Measurement Of Subcellular Ca2+ Redistribution In Cardiac Muscle In Situ: Time Resolved Rapid Freezing And Electron Probe Microanalysis, Meredith Bond, Mark D. Schluchter, Eva Keller, Christine S. Moravec

Scanning Microscopy

To directly assess the physiological roles of sarcoplasmic reticulum (SR) and miitochondria (MT), we have utilized energy dispersive electron probe microanalysis (EPMA) on ultrathin freeze-dried cryosections from isolated papillary muscles, rapidly frozen at precise time points of the contractile cycle. Using this approach, we can detect redistribution of subcellular Ca2+ during the cardiac contractile cycle. Changes in Ca2+ of less than 1.0 mmol/kg dry wt can be detected. By determining the variability of the Ca2+ measurements in preliminary experiments, we have also demonstrated that it is possible to optimize experimental design, i.e., to predict the number of …