scholarly journals Double staining procedure for histochemical localization of alcohol and aldehyde dehydrogenase activities in the mouse liver.

1989 ◽  
Vol 22 (3) ◽  
pp. 401-406 ◽  
Author(s):  
TOSHIMITSU WATABIKI ◽  
TAKUMA TOKIYASU ◽  
NORIAKI ISHIDA ◽  
KAZUO OGAWA
Author(s):  
Jane E. Ramberg ◽  
Shigeto Tohma ◽  
Peter E. Lipsky

Intercellular adhesion molecule (ICAM-1) appears to be a ligand for LFA-1 dependent adhesion in T cell mediated cytotoxcity. It is found on cells of both hematopoietic and non-hematopoietic origin. While observing the activity of ICAM-1 on the surfaces of interacting T and B cells, we found that we could successfully carry out a pre-embedding double staining procedure utilizing both colloidal gold and peroxidase conjugated reagents.On 24-well microtiter plates, mitomycin-treated T4 cells were stimulated with 64.1 (anti-CD3) for one hour before the addition, in some instances, of B cells. Following a 12-48 hour incubation at 38°C, the cells were washed and then immunostained with a colloidal gold conjugated RFB-4 (anti-CD22); biotinylated R6.5 (anti-ICAM-1); followed by streptavidin/peroxidase. This method allowed us to observe two different antigens without concern about possible cross-reaction of reagents. Because we suspected ICAM-1 and R6.5 were sensitive to fixation, we tried varying concentrations of fresh paraformaldehyde before R6.5, after R6.5 and after streptavidin/peroxidase. All immunostaining and washing was done on ice with ice cold reagents.


1979 ◽  
Vol 55 (2) ◽  
pp. 105-108
Author(s):  
E F Hunter ◽  
R M McKinney ◽  
S E Maddison ◽  
D D Cruce

1993 ◽  
Vol 41 (4) ◽  
pp. 627-630 ◽  
Author(s):  
S Würden ◽  
U Homberg

We have developed a new double immunofluorescence technique by which two neuroactive substances in the same tissue section can be labeled with primary antisera raised in the same species. The optic lobes of the locust Schistocerca gregaria were used as a model system to develop the staining procedure. FMRFamide-immunoreactive neurons were detected by rabbit antisera against FMRFamide and FITC-conjugated secondary antibodies. Antibodies against the second peptide, pigment-dispersing hormone (PDH), also raised in rabbit, were biotinylated and detected via streptavidin-Texas Red. Crossreactivity of the PDH immunoglobulins with the FITC-conjugated secondary antiserum was prevented by pre-incubation with rabbit gamma globulins. The two peptide immunoreactivities could be conveniently observed on the same section with the different fluorescent markers. This double labeling technique with modified antibodies is easily performed and highly useful for co-localization studies with antisera raised in the same species.


1981 ◽  
Vol 31 ◽  
pp. 258
Author(s):  
Hiromi Yamazaki ◽  
Keiko Nishiguchi ◽  
Suehiro Nakanishi

1986 ◽  
Vol 31 (2) ◽  
pp. 205-211 ◽  
Author(s):  
Raymond E. Richmond ◽  
Michael A. Pereira

Cytometry ◽  
1991 ◽  
Vol 12 (4) ◽  
pp. 366-372 ◽  
Author(s):  
P. J. M. Bakker ◽  
J. Stap ◽  
C. J. Tukker ◽  
C. H. van Oven ◽  
C. H. N. Veenhof ◽  
...  

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