Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-26T05:29:22.687Z Has data issue: false hasContentIssue false
  • English
  • Français

SEM Processing Of Blood Samples

Published online by Cambridge University Press:  14 March 2018

Sara E. Miller
Sara E. Miller*
Affiliation:
Duke University Medical School

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A long time ago, we ciid some work on RBC's from muscular dystrophy patients, We found that the cells are very sensitive to pH, salt concentration, glass, and other things (maybe including the moon???), Low pH, increased salt, especially NaCl, and sitting in a glass tube or on a glass slide unfixed would cause echinocyte formation.

We got around the problem by drawing the blood and then IMMEDIATELY dropping (drop by drop) blood samples into 1% glutaraldehyde in phosphate buffer, pH 7.4 (not PBS). You can use a Maunsbach formula, where 0.135 U P04 gives 300 milliosmoles, or 0.1 M P04 plus sucrose (try 1.8 % sucrose). Test the osmolarity of the buffer; it should be 300 ± 10 or so. The final osmolarity of the buffered fix will be 400 milliosmoles; 300 from the buffer and 100 from the glutaraldehyde! The fix should be room temperature (not cold) when the blood is added. It can be stored refrigerated.

Type
Research Article
Information
Microscopy Today , Volume 6 , Issue 1 , January 1998 , pp. 19
Copyright
Copyright © Microscopy Society of America 1998

References

Miller, S.E., Roses, A.D. and Appel, S.H., 1975. Erythrocytes in human muscular dystrophy, Science 188:1131.Google Scholar
Roses, A. D., Appet, S. H., Butterfield, D. A., Miller, S. E. and Chesnut, D. B.. 1975. Specificity of biochemical and biophysical tests in Duchenne and myotonic muscular dystrophy, carrier states and congenital myotonia. Trans. Amer. Neurol. Assoc. 100:131–134.Google Scholar
Roses, A.O., Roses, M.J., Miller, S.E., Hull, K.J. Jr. and Appel, S.H., 1976, Carrier detection in Duchenne muscular dystrophy, New Engl. J. Med. 294:193–198.Google Scholar
Miller, S.E., Roses, A D. and Appel, S. H. 1976. Scanning electron microscopy studies in muscular dystrophy. Arch. Neurol. 33:172–174.Google Scholar