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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
1985-9-4
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pubmed:abstractText |
Immunofluorescence microscopy of cultured animal cells is often performed after detergent permeabilization of formaldehyde-fixed cellular membranes so that antibodies may have access to intracellular antigens. A comparison was made of the ability of several detergents, after formaldehyde fixation, to affect localization of intracellular proteins or to permeabilize different organelles to antibodies. Saponin, a detergent-like molecule that can permeabilize cholesterol-containing membranes, was also used. Four monoclonal antibodies were found to have a bright, discrete fluorescence localization with saponin alone, but were almost undetectable when the cells were treated with nonionic detergents such as Triton X-100 or NP-40. These immunoglobulin G antibodies included two against lysosomal membrane glycoproteins, one against an integral membrane protein found in the plasma membrane and endocytic vesicles, and one against a membrane protein in the endoplasmic reticulum and the nuclear envelope. However, antigens localized in mitochondria and the nucleus required the use of a detergent such as Triton X-100 for their detection. The detection of a number of other membrane or cytoplasmic proteins was unaffected by Triton X-100 treatment. It was concluded that nonionic detergents such as Triton X-100 cause artifactual loss of detection of some membrane proteins, and saponin is a favorable alternative reagent for immunofluorescence detection of intracellular membrane antigens in many organelles.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Detergents,
http://linkedlifedata.com/resource/pubmed/chemical/Formaldehyde,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Octoxynol,
http://linkedlifedata.com/resource/pubmed/chemical/Polyethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Saponins
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0022-1554
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
813-20
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3894499-Animals,
pubmed-meshheading:3894499-Antibodies, Monoclonal,
pubmed-meshheading:3894499-Cell Line,
pubmed-meshheading:3894499-Cricetinae,
pubmed-meshheading:3894499-Detergents,
pubmed-meshheading:3894499-Fluorescent Antibody Technique,
pubmed-meshheading:3894499-Formaldehyde,
pubmed-meshheading:3894499-Membrane Proteins,
pubmed-meshheading:3894499-Methods,
pubmed-meshheading:3894499-Mice,
pubmed-meshheading:3894499-Octoxynol,
pubmed-meshheading:3894499-Polyethylene Glycols,
pubmed-meshheading:3894499-Rabbits,
pubmed-meshheading:3894499-Rats,
pubmed-meshheading:3894499-Saponins
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pubmed:year |
1985
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pubmed:articleTitle |
Postfixation detergent treatment for immunofluorescence suppresses localization of some integral membrane proteins.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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