1977
DOI: 10.1136/jcp.30.2.138
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A shorter immunoperoxidase technique for the demonstration of carcinoembryonic antigen and other cell products.

Abstract: A reliable immunoperoxidase schedule for the cellular demonstration of tumour and normal cell products which can be completed in well under two hours is described. The preparations are as clear and readable as those stained by routine histological techniques and should form a valuable adjunct in research and diagnostic studies.

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Cited by 165 publications
(50 citation statements)
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“…Although Triton does cause some damage to liver parenchymal cells (Cotmore & Carter, 1973), the effect on the galactosereceptor function was minimal and asialo-glycoprotein uptake was normal, though it is possible that subsequent inhibition of lysosomal digestion of the glycoproteins may have occurred. It can be seen from the above data that removal of sialic acid from carcinoembryonic antigen in itself does not affect Kupffer-cell uptake, but when terminal galactose residues are exposed the uptake by hepatocytes becomes important and in general the majority of the circulating asialo-glycoprotein is now removed by this route and may be observed by radioautography of the 125I-labelled molecule (Thomas et al, 1977), or by immunoperoxidase staining (Heyderman & Neville, 1977; E. Heyderman & P. Thomas, un- This would give further support to the suggestion that biliary excretion occurs via a different mechanism from direct Kupffer-cell or parenchymal-cell uptake (Thomas & Summers, 1978).…”
Section: Methodsmentioning
confidence: 95%
“…Although Triton does cause some damage to liver parenchymal cells (Cotmore & Carter, 1973), the effect on the galactosereceptor function was minimal and asialo-glycoprotein uptake was normal, though it is possible that subsequent inhibition of lysosomal digestion of the glycoproteins may have occurred. It can be seen from the above data that removal of sialic acid from carcinoembryonic antigen in itself does not affect Kupffer-cell uptake, but when terminal galactose residues are exposed the uptake by hepatocytes becomes important and in general the majority of the circulating asialo-glycoprotein is now removed by this route and may be observed by radioautography of the 125I-labelled molecule (Thomas et al, 1977), or by immunoperoxidase staining (Heyderman & Neville, 1977; E. Heyderman & P. Thomas, un- This would give further support to the suggestion that biliary excretion occurs via a different mechanism from direct Kupffer-cell or parenchymal-cell uptake (Thomas & Summers, 1978).…”
Section: Methodsmentioning
confidence: 95%
“…Endogenous peroxidase was abolished by the hydrogen peroxide-periodic acidborohydride sequence (Heyderman & Neville, 1977 (Altmannsberger et al, 1981), gives a weak but specific staining of breast cancer metastatic cells also in formalin-fixed tissues.…”
Section: Methodsmentioning
confidence: 99%
“…-Approximately 4,um sections were dewaxed, bleached in a solution of hydrogen peroxide and treated with periodic acid, followed by borohydride (Heyderman & Neville, 1976). Sections were then incubated with a suitable dilution of rabbit antiserum for 90 min, -washed and incubated with the enzyme-conjugated second antibody for a further hour and a half.…”
mentioning
confidence: 99%