scholarly journals Immunohistochemical/histochemical double staining method in the study of the columnar metaplasia of the oesophagus

2014 ◽  
Vol 58 (1) ◽  
Author(s):  
D. Cabibi ◽  
A.G. Giannone ◽  
C. Mascarella ◽  
C. Guarnotta ◽  
M. Castiglia ◽  
...  
Author(s):  
Seiji Kato

Previously, the author repeatedly confirmed the higher 5’-nucleotidase (5’-Nase) and lower alkaline phoaphatase (ALPase) activities in the wall of lymphatic capillaries reacted with the lead-based method relative to those of blood capillaries. The ALPase, on the other hand, is markedly higher in blood capillaries than in lymphatics. On the basis of these enzyme characteristics, the author has developed a 5’-Nase— ALPase double staining method to differentiate small lymphatics from blood capillaries at the level of the light microcsopy. Furthermore, we applied it to histochemical observation of the lead-containing reaction products of 5’-Nase in lymphatics on the same or adjacent cryostat sections using backscattered electron imaging (BEI) in scanning electron microscope (SEM). This paper presents a new applicability of 5’-Nase histochemistry by BEI-SEM to demonstrate the distribution of lymphatic capillaries in tissue blocks.


1993 ◽  
Vol 6 (1) ◽  
pp. 77
Author(s):  
Hong-Shang Hong ◽  
Yu-Shung Lee ◽  
Heng-Leong Chan ◽  
Tseng-tong Kuo

1980 ◽  
Vol 28 (5) ◽  
pp. 469-471 ◽  
Author(s):  
F Vandesande ◽  
K Dierickx ◽  
N Goossens

Serial sections of vertebrate hypothalami were stained with the immunocytochemical peroxidase-antiperoxidase method. In addition to the single staining method, our double staining method was used, which enabled us to visualize two tissue antigens in single tissue sections. In both staining methods, differentially adsorbed antineurohypophysial hormone sera, anti-somatostatin serum and anti-bovine neurophysin sera were used. The results confirm the one hormone, one neuron hypothesis.


1968 ◽  
Vol 55 (10) ◽  
pp. 496-497 ◽  
Author(s):  
Sibdas Ghosh ◽  
Renate Lettr�

1990 ◽  
Vol 38 (3) ◽  
pp. 325-329 ◽  
Author(s):  
W van den Brink ◽  
C van der Loos ◽  
H Volkers ◽  
R Lauwen ◽  
F van den Berg ◽  
...  

A combination of beta-galactosidase enzyme and the immunogold/silver staining method was studied for evaluation of double-staining experiments. Applications are shown for immunohistochemical double staining using two monoclonal antibodies and for combined immunohistochemistry and DNA in situ hybridization in one tissue section. The following advantages for the present double-staining method were evaluated: superior sensitivity of the immunogold/silver staining method for at least one epitope, which also allows detection of biotinylated DNA probes. The structure of the indolyl precipitate after revelation of beta-galactosidase activity did not show a concealing effect during a sequential double-staining method, as compared with the visualization of peroxidase with diaminobenzidine. These factors, and the sharply contrasting colored reaction products of beta-galactosidase (blue-green) and the immunogold/silver staining method including silver enhancement (brown-black), allow clear distinction of mixed-stained cell constituents.


2010 ◽  
Vol 5 (3) ◽  
Author(s):  
T. Matsushita ◽  
Y. Kobayashi ◽  
K. Nakamura ◽  
Y. Matsui ◽  
K. Ohno

The mechanisms of increase in geosmin concentration in MF permeate with filtration time were investigated when inflow to the MF contained cyanobacteria incorporating geosmin inside and outside their cells. Whereas the geosmin concentration in the MF permeate was almost the same as the extracellular geosmin concentration in the MF inflow at the beginning of filtration, it increased and exceeded the extracellular geosmin concentration in MF inflow after 2 h of filtration. A cell viability test using a double-staining method revealed that a portion of the intracellular geosmin, which was incorporated in the cyanobacterial cells and therefore retained on the MF membrane, was released from the cells. This occurred probably because increased transmembrane pressure (TMP) with filtration time forced the cells to compress. However, geosmin release was not explained simply by cell breakage: other possible factors were implied.


1989 ◽  
Vol 91 (1) ◽  
pp. 47-50 ◽  
Author(s):  
E. Kerem ◽  
D. Schwartz-Arad ◽  
E. Bartfeld ◽  
N. Ron ◽  
I. Ariel ◽  
...  

1999 ◽  
Vol 32 (4) ◽  
pp. 327-332 ◽  
Author(s):  
Tetsunari Nishikawa ◽  
Shoichi Arai ◽  
Kenichi Uobe ◽  
Masahiro Wato ◽  
Kazuya Tominaga ◽  
...  

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