Access the full text.
Sign up today, get DeepDyve free for 14 days.
E. Helinski, G. Bootsma, R. McGroarty, G. Ovak, É. Harven, J. Pauly (1990)
Scanning electron microscopic study of immunogold-labeled human leukocytes.Journal of electron microscopy technique, 14 4
J. William, Todd, George Wray, P. Hitchcock (1984)
Arrangement of pili in colonies of Neisseria gonorrhoeaeJournal of Bacteriology, 159
J. Swanson (1972)
Studies on gonococcus infection. II. Freeze‐fracture, freeze‐etch studies of gonococci, 136
J. Swanson (1972)
STUDIES ON GONOCOCCUS INFECTIONThe Journal of Experimental Medicine, 136
A. Boyde, E. Maconnachie (1981)
Morphological correlations with dimensional change during SEM specimen preparation, 3
D. Bessen, E. Gotschlich (1987)
Chemical characterization of binding properties of opacity-associated protein II from Neisseria gonorrhoeaeInfection and Immunity, 55
A. L. Cohen (1979)
Critical point drying—principles and procedures, 2
J. Nation (1983)
A new method using hexamethyldisilazane for preparation of soft insect tissues for scanning electron microscopy.Stain technology, 58 6
H. Ris (1985)
The cytoplasmic filament system in critical point-dried whole mounts and plastic-embedded sectionsThe Journal of Cell Biology, 100
D. Schroeter, E. Spiess, N. Paweletz, R. Benke (1984)
A procedure for rupture-free preparation of confluently grown monolayer cells for scanning electron microscopyJournal of Electron Microscopy Technique, 1
J. Swanson (1977)
Surface components affecting interactions between Neisserai gonorrhoeae and eucaryotic cells.The Journal of infectious diseases, 136 Suppl
T. Elmros, P. Hörstedt, B. Winblad (1975)
Scanning electron microscopic study of virulent and avirulent colonies of Neisseria gonorrhoeaeInfection and Immunity, 12
A. Boyde (1978)
Pros and cons of critical point drying and freeze drying for SEM, 2
J. Heckels (1989)
Structure and function of pili of pathogenic Neisseria speciesClinical Microbiology Reviews, 2
S. Kraus, L. Glassman (1974)
Scanning Electron Microscope Study of Neisseria gonorrhoeaeApplied Microbiology, 27
J. Kennedy, R. Williams, J. Gray (1989)
Use of Peldri II (a fluorocarbon solid at room temperature) as an alternative to critical point drying for biological tissues.Journal of electron microscopy technique, 11 2
W. Burnette (1981)
"Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A.Analytical biochemistry, 112 2
Kenneth Miller, Cynthia Prescott, Teresa Jacobs, N. Lassignal (1983)
Artifacts associated with quick-freezing and freeze-drying.Journal of ultrastructure research, 82 2
L. Wollweber, R. Stracke, U. Gothe (1981)
The use of a simple method to avoid cell shrinkage during SEM preparationJournal of Microscopy, 121
Debra Gusnard, R. Kirschner (1977)
Cell and organelle shrinkage during preparation for scanning electron microscopy: effects of fixation, dehydration and critical point dryingJournal of Microscopy, 110
R. Albrecht, D. Rasmussen, C. Keller, R. Hinsdill (1976)
Preparation of cultured cells for SEM: air drying from organic solventsJournal of Microscopy, 108
U. Laemmli (1970)
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 227
H. Sidberry, Bennett Kaufman, D.Craig Wright, Jerald Sadoff (1985)
Immunoenzymatic analysis by monoclonal antibodies of bacterial lipopolysaccharides after transfer to nitrocellulose.Journal of immunological methods, 76 2
M. A. Hayat, S. E. Miller (1990)
Negative Staining
Piliated Neisseria gonorrhoeae are virulent and attach readily to some human mucosal cells. The study of interactions between piliated Neisseria gonorrhoeae and surface structures of eukaryotic cells in tissue culture requires consistent high resolution imaging in scanning electron microscopy (SEM). The combination of the fixatives glutaraldehyde, osmium, tannic acid, and uranyl acetate improves preservation of pili and other delicate structures. Following the critical point drying (CPD) process, pili bundles remained intact, but charging produced image distortion in most of the specimens. The use of hexamethyldisilazane (HMDS) with air drying substantially reduced charging and image distortion. Less contrast and greater resolution of pili bundles and surface structures of bacteria or tissue culture cells were obtained at magnifications of 10,000 or higher. As an alternative to CPD, HMDS processing of cell culture monolayers was simple and was more efficient when a large number of samples was processed.
Microscopy Research and Technique – Wiley
Published: Dec 1, 1991
Keywords: ; ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.