Immunoenzyme technique

Author(s):  
C.F.A. Culling ◽  
R.T. Allison ◽  
W.T. Barr
1987 ◽  
Vol 33 (2) ◽  
pp. 149
Author(s):  
L. Pötsch-Schneider ◽  
L. Penzes

1973 ◽  
Vol 51 (2) ◽  
pp. 368-382 ◽  
Author(s):  
William H. Fishman ◽  
John P. Manning ◽  
M. Takeda ◽  
Dennis Angellis ◽  
Sidney Green

1988 ◽  
Vol 36 (8) ◽  
pp. 983-989 ◽  
Author(s):  
S Yokota ◽  
J Oka ◽  
H Ozasa ◽  
R Itoh

We investigated the localization of cytosol 5'-nucleotidase in chicken liver by use of a pre-embedding immunoenzyme technique. Cytosol 5'-nucleotidase was purified from chicken liver and a monospecific antibody to this enzyme was raised in a rabbit. Fab fragments of the antibody were conjugated with horseradish peroxidase. Tissue sections of the fixed chicken liver were incubated with the peroxidase-Fab fragments, followed by DAB reaction for peroxidase. By light microscopy, dark-brown staining was present in the cytoplasm of parenchymal cells, Kupffer cells, and endothelial cells. The latter two types of cells were stained more strongly than the former. By electron microscopy, reaction deposits were present in the cytoplasmic matrix but not in cell organelles, such as mitochondria, endoplasmic reticulum, and peroxisomes, or in nuclei. In control sections incubated with peroxidase-conjugated Fab fragments from non-immunized rabbit, no specific reaction was noted. The results indicate that cytosol 5'-nucleotidase is contained more in the sinus-lining cells and less in the parenchymal cells, and that the enzyme is present in the cytoplasmic matrix of these cells.


1978 ◽  
Vol 102 (21) ◽  
pp. 462-463 ◽  
Author(s):  
J. Roszkowski ◽  
M. Bartoszcze ◽  
J. Zadura ◽  
Z. Swiatek

1986 ◽  
Vol 34 (7) ◽  
pp. 891-897 ◽  
Author(s):  
S Yokota ◽  
H Tsuji ◽  
K Kato

Localization of cathepsin B in rat kidney was studied using immunocytochemical techniques. Cathepsin B was purified from rat liver and antibody to it was raised in rabbits. The antibody reacted with a lysosomal extract of rat kidney to form a single precipitin line in a double-diffusion test. Immunoblot analysis of lysosomal cathepsin B of rat kidney showed two species of 29K and 25K MW. After removal of Epon, semi-thin sections of glutaraldehyde-fixed tissue were stained by the indirect immunoenzyme technique. Dark-brown reaction product, indicating the antigenic sites for cathepsin B, was found in cytoplasmic granules throughout the nephron. Staining intensity and size of the positive granules varied widely in each segment of the nephron. In the glomeruli and distal tubules, a few small cytoplasmic granules were stained. In the proximal tubules, the S1 segment exhibited many large granules which were most heavily stained, whereas the S2 and S3 segments contained few positive granules. All segments of the distal tubules showed the smallest amount of positive granules. A few positive granules were also noted in the cortical and medullary collecting tubules. Control experiments confirmed the specificity of the staining. The results indicate that the major site for cathepsin B in rat kidney is the S1 segment of the proximal tubule which is known to actively take up proteins leaked through the glomerulus.


Sign in / Sign up

Export Citation Format

Share Document