Axonal branching of medullary swallowing neurons projecting on the trigeminal and hypoglossal motor nuclei: demonstration by electrophysiological and fluorescent double labeling techniques

1990 ◽  
Vol 81 (2) ◽  
Author(s):  
M. Amri ◽  
A. Car ◽  
C. Roman
Keyword(s):  
Double Labeling ◽  
Axonal Branching ◽  
Motor Nuclei

Axonal branching of the olivocerebellar projection in the rat: A double-labeling study

1989 ◽  
Vol 284 (1) ◽  
pp. 48-59 ◽  
Author(s):  
A. W. Hrycyshyn ◽  
H. Ghazi ◽  
B. A. Flumerfelt
Keyword(s):  
Double Labeling ◽  
Axonal Branching

scholarly journals Cerebellar afferents from neurons in the extraocular motor nuclei: A fluorescent retrograde double-labeling study in the sheep

1999 ◽  
Vol 254 (4) ◽  
pp. 490-495 ◽  
Author(s):  
Maria Luisa Lucchi ◽  
Anna Maria Barazzoni ◽  
Paolo Clavenzani ◽  
Roberto Chiocchetti ◽  
Paolo Berardinelli ◽  
...  
Keyword(s):  
Double Labeling ◽  
Cerebellar Afferents ◽  
Motor Nuclei

Axonal branching of basal forebrain projections to the neocortex: a double-labeling study in the cat

1986 ◽  
Vol 375 (1) ◽  
pp. 176-181 ◽  
Author(s):  
Marea K. Boylan ◽  
Robin S. Fisher ◽  
Chester D. Hull ◽  
Nathaniel A. Buchwald ◽  
Michael S. Levine
Keyword(s):  
Basal Forebrain ◽  
Double Labeling ◽  
Axonal Branching

Double-labeling study of axonal branching within the lateral reticulocerebellar projection in the rat

1987 ◽  
Vol 258 (3) ◽  
pp. 378-386 ◽  
Author(s):  
H. Ghazi ◽  
A. W. Hrycyshyn ◽  
B. A. Flumerfelt
Keyword(s):  
Double Labeling ◽  
Axonal Branching

Gold labeling of teichoic acid on adjacent surfaces of staphylococcus aureus

1990 ◽  
Vol 48 (3) ◽  
pp. 578-579
Author(s):  
Margaret Hukee
Keyword(s):  
Staphylococcus Aureus ◽  
Teichoic Acid ◽  
Protein Labeling ◽  
Minimal Amount ◽  
Section Thickness ◽  
Double Labeling ◽  
Parallel Surfaces ◽  
Supporting Membrane

Gold labeling of two antigens (double labeling) is often done on two section surfaces separated by section thickness. Whether labeling is done on both sides of the same section or on two parallel surfaces separated by section thickness (PSSST), comparable results are dependent on an equal number of epitopes being exposed at each surface. We propose a method to study protein labeling within the same field of proteins, by examining two directly adjacent surfaces that were split during sectioning. The number of labeling sites on adjacent surfaces (AS) were compared to sites on PSSST surfaces in individual bacteria.Since each bacteria needed to be recognizable in all three section surfaces, one-hole grids were used for labeling. One-hole grids require a supporting membrane and excessive handling during labeling often ruptures the membrane. To minimize handling, a labeling chamber was designed that is inexpensive, disposable, minimizes contamination, and uses a minimal amount of solution.

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