scholarly journals Antibody Conjugation and CODEX Multiplexed Immunofluorescence of Fresh Frozen Tissue v1

protocols.io ◽  
2021 ◽  
Author(s):  
Elizabeth Neumann ◽  
Carrie not provided Romer ◽  
Nathan Heath Patterson ◽  
Jamie Allen ◽  
Jeff Spraggins
1988 ◽  
Vol 25 (1) ◽  
pp. 77-82 ◽  
Author(s):  
K. G. Braund ◽  
K. A. Amling

Skeletal muscle samples from two healthy dogs were stored in ice at 0 C for up to 30 hours to examine the influence of time on cell morphology and morphometry. Cytochemical and histochemical properties of muscle to 18 hours were not markedly different from fresh frozen tissue. Samples stored to 30 hours were still satisfactory, despite a decline and unevenness in depth of staining. Morphometry from samples stored at 0 C for 6 hours or longer is not recommended, due to the statistically significant increase in diameter (from 21 to 25%) of type I and type II fibers.


protocols.io ◽  
2019 ◽  
Author(s):  
Maya Brewer ◽  
Yuantee Zhu ◽  
Elizabeth Neumann ◽  
Danielle Gutierrez ◽  
Jeff Spraggins ◽  
...  
Keyword(s):  

Author(s):  
Y. Krivosic ◽  
M. Jomin ◽  
J. L. Christiaens ◽  
P. Dhellemmes ◽  
G. Combelles ◽  
...  

Blood ◽  
1965 ◽  
Vol 26 (2) ◽  
pp. 215-219 ◽  
Author(s):  
LEONARD S. KAPLOW ◽  
Charlotte Ladd

Abstract A method is described for demonstrating leukocyte peroxidase activity in which benzidine dihydrochloride is used as the indicator compound instead of the more commonly used but potentially more hazardous benzidine base. The method is highly sensitive and rapid and permits the use of fixed blood smears and organ imprints. The incubation mixture, which incorporates safranin as a counterstain, may be used over and over again, for as long as 6 months. The method is also applicable to fresh frozen tissue sections.


PLoS ONE ◽  
2015 ◽  
Vol 10 (12) ◽  
pp. e0144162 ◽  
Author(s):  
Ensel Oh ◽  
Yoon-La Choi ◽  
Mi Jeong Kwon ◽  
Ryong Nam Kim ◽  
Yu Jin Kim ◽  
...  

2017 ◽  
Vol 18 (3) ◽  
pp. 425-431 ◽  
Author(s):  
Z. S. Lalmahomed ◽  
◽  
R. R. J. Coebergh van den Braak ◽  
M. H. A. Oomen ◽  
S. P. Arshad ◽  
...  

1984 ◽  
Vol 32 (6) ◽  
pp. 636-642 ◽  
Author(s):  
P M Frederik ◽  
P H Bomans ◽  
W M Busing ◽  
R Odselius ◽  
W M Hax

Several organic and inorganic vapor fixatives have been tested for their ability to stabilize the ultrastructure of freeze-dried thin cryosections. The vapors from osmium tetroxide and dry formaldehyde gave a good preservation of the ultrastructure. Fixation in formaldehyde vapor preserved the immunoreactivity of alpha-amylase in exocrine pancreas, as was demonstrated with an indirect labeling technique using anti-alpha-amylase and protein A-gold. A major advantage of the use of vapor fixation is that cryosections from a specimen of fresh-frozen tissue can be used for immunocytochemistry as well as for X-ray microanalysis, as was demonstrated for the exocrine pancreas. This opens the possibility of localizing atomic species (X-ray microanalysis) and molecular species (immunocytochemistry) at the subcellular level on thin cryosections from the same tissue block.


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