1981
DOI: 10.1007/bf00495658
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Postembedding immunohistochemical demonstration of antigen in experimental polyarthritis using plastic embedded whole joints

Abstract: A method is presented for the immunohistochemical demonstration of antigens in whole undecalcified joints of small laboratory animals. With this method of tissue preparation, involving embedding in a medium mainly based on 2-hydroxyethyl methacrylate, preservation of antigenicity is satisfactory. Antigens can be demonstrated in 2 micron sections by either immunofluorescence or immunoperoxidase and an indirect technique. Therefore in addition to the morphological analysis of joint alterations in experimental po… Show more

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Cited by 57 publications
(26 citation statements)
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“…Samples were fixed in paraformaldehyde (4%) for 24 to 48 hours and subsequently embedded in paraffin and plastic. 24 Sections of 5 mm and 2 mm were routinely stained with HE, according to Giemsa and periodic acid-Schiff (PAS), reaction and examined by light microscopy. Selected skin sections of SA 6, SA 20, and SA 22 taken during subacute and chronic stages were also stained with Masson's trichrome stain and picrosirius red/Alcian blue.…”
Section: Skin Sample Collection and Tissue Preparationmentioning
confidence: 99%
“…Samples were fixed in paraformaldehyde (4%) for 24 to 48 hours and subsequently embedded in paraffin and plastic. 24 Sections of 5 mm and 2 mm were routinely stained with HE, according to Giemsa and periodic acid-Schiff (PAS), reaction and examined by light microscopy. Selected skin sections of SA 6, SA 20, and SA 22 taken during subacute and chronic stages were also stained with Masson's trichrome stain and picrosirius red/Alcian blue.…”
Section: Skin Sample Collection and Tissue Preparationmentioning
confidence: 99%
“…For scientific interest, a ~2 cm 3 specimen was excised from the periphery of the white, multilobulated tumour and fixed in 10% formalin for histopathological evaluation. Sections of paraffin-embedded samples and of glycolmethacrylate/methylmethacrylate-embedded samples (Hermanns et al 1981) were routinely prepared and stained with haematoxylin and eosin (HE) and reticulin preparation. Immunostaining of cytokeratin, vimentin, desmin, actin, calponin, MAC387 and lysozyme was performed using horseradish peroxidase-coupled secondary antibodies r,s .…”
Section: Case Descriptionmentioning
confidence: 99%
“…Cytology (Diff-Quick staining kit, Fisher Scientific GmbH, Schwerte, Germany) of an impression smear showed a moderate number of mostly degenerated neutrophils, plasma cells and clusters of polygonal epithelial cells. For histopathological examination, specimens of the excised mass were fixed in 10 per cent buffered formaldehyde and routinely embedded in paraffin and glycolmethacrylate/methylmethacrylate (Hermanns et al, 1981). Histologically, the mass was composed of a fibrous connective tissue stroma with decent, accentuated subepithelial infiltration of neutrophils, macrophages, lymphocytes and plasma cells, and few foci of calcification and cholesterol clefts.…”
Section: Case Descriptionmentioning
confidence: 99%