scholarly journals Estimation of Bacterial Biovolume and Biomass by Scanning Electron Microscopic Image Analysis.

1996 ◽  
Vol 11 (1) ◽  
pp. 11-17 ◽  
Author(s):  
KATSUJI TANI ◽  
JI MIN CHEN ◽  
NOBUYASU YAMAGUCHI ◽  
MASAO NASU
Keyword(s):  
Image Analysis ◽  
Microscopic Image ◽  
Electron Microscopic ◽  
Microscopic Image Analysis ◽  
Scanning Electron Microscopic ◽  
Electron Microscopic Image ◽  
Scanning Electron Microscopic Image ◽  
Scanning Electron

scholarly journals Leukemic Reticuloendotheliosis

Blood ◽  
1971 ◽  
Vol 38 (3) ◽  
pp. 288-298 ◽  
Author(s):  
SIDNEY TRUBOWITZ ◽  
BERTHA MASEK ◽  
JULIO M. FRASCA
Keyword(s):  
Time Lapse ◽  
Electron Microscopic ◽  
Scanning Electron Microscopic ◽  
Electron Microscopic Image ◽  
Functional Features ◽  
Reticular Cells ◽  
Hairy Cells ◽  
Phase Transmission ◽  
Scanning Electron Microscopic Image ◽  
Scanning Electron

Abstract The anatomical and functional features of the hairy cells of leukemic reticuloendothelisis were investigated by time lapse cinematography; phytohemagglutinin stimulation; adherence to siliconized surfaces; a variety of cytochemical methods; and phase, transmission, and scanning electron microscopy. The scanning electron microscopic image supports the morphologic evidence for a relationship between the hairy and the reticular cells.

Preparation of Articular Cartilage for Scanning Electron Microscopy

1973 ◽  
Vol 31 ◽  
pp. 436-437
Author(s):  
M. L. Zimny ◽  
I. Redler ◽  
J. Fernandez
Keyword(s):  
Articular Cartilage ◽  
Femoral Condyle ◽  
Tissue Preparation ◽  
Electron Microscopic ◽  
Tissue Samples ◽  
Scanning Electron Microscopic ◽  
Electron Microscopic Image ◽  
The Relationship ◽  
Scanning Electron Microscopic Image ◽  
Scanning Electron

The relationship between tissue preparation and a scanning electron microscopic image is still somewhat nebulous. For purposes of answering comments about our observations of articular cartilage, we decided to prepare tissue samples from one area of a femoral condyle, obtained at surgery, in several ways. As a result of this investigation we hoped to find the best way to prepare articular cartilage for maximal visual detail and subsequently standardize our procedures for a comparative study of normal and arthritic cartilage.The samples were fixed as follows: (1) no fixative; (2) 2% glutaraldehyde buffered with cacodylate, pH 7.4; (3) 10% buffered formalin; (4) 0.1% glutaraldehyde in Ringer's; and (5) 1% glutaraldehyde in Ringer's.

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