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pubmed-article:3217949pubmed:abstractTextMicrowave irradiation as a means of fixation was evaluated for the preservation of extracellular matrix antigens such as collagen III, IV, fibronectin and laminin in both lung and liver specimens. Small tissue samples were placed in normal saline or periodate-lysine-paraformaldehyde (PLP) and irradiated for 30 sec to bring them to a temperature of 50 C. The tissue was then processed rapidly in a tissue processor adjusted to a 2 hr cycle and embedded in paraffin. Sections were immunostained. For comparison, routine cryostat sections as well as sections of formalin fixed tissue were used. Microwave irradiation in saline gave excellent morphological detail, comparable to that in formalin fixed tissue. All four antigens evaluated were well preserved without the necessity of prior pepsin digestion. Microwave fixation is promising for preservation of antigenicity and morphological detail, and considerably reduces the time required for processing.lld:pubmed
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pubmed-article:3217949pubmed:authorpubmed-author:JagirdarJJlld:pubmed
pubmed-article:3217949pubmed:authorpubmed-author:NelsonFFlld:pubmed
pubmed-article:3217949pubmed:authorpubmed-author:MoranR ARAlld:pubmed
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pubmed-article:3217949pubmed:volume63lld:pubmed
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pubmed-article:3217949pubmed:pagination263-9lld:pubmed
pubmed-article:3217949pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:3217949pubmed:year1988lld:pubmed
pubmed-article:3217949pubmed:articleTitleApplication of microwave irradiation to immunohistochemistry: preservation of antigens of the extracellular matrix.lld:pubmed
pubmed-article:3217949pubmed:affiliationImmunopathology Laboratory, Veterans Administration Medical Center, Bronx, New York.lld:pubmed
pubmed-article:3217949pubmed:publicationTypeJournal Articlelld:pubmed
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