1986
DOI: 10.1679/aohc.49.391
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Serial semithin sections in immunohistochemistry : Techniques and applications.

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Cited by 66 publications
(40 citation statements)
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“…B. A. S., ZeissKontron, Germany; see GRUBE and KUSUMOTO, 1986;EHRHART et al, 1988). According to the findings so far obtained in G and A cells, a relatively high proportion of these cells exhibits this reciprocal relation between CgA-and peptide-immunoreactivities.…”
Section: Interrelations Of Cga With Peptide Hormonesmentioning
confidence: 88%
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“…B. A. S., ZeissKontron, Germany; see GRUBE and KUSUMOTO, 1986;EHRHART et al, 1988). According to the findings so far obtained in G and A cells, a relatively high proportion of these cells exhibits this reciprocal relation between CgA-and peptide-immunoreactivities.…”
Section: Interrelations Of Cga With Peptide Hormonesmentioning
confidence: 88%
“…We used a limited number of polyclonal antisera against bovine and rat Cg (source: D. Aunis, Strasbourg, France; H. Winkler, Innsbruck, Austria) that have been characterized immunologically and immunohistochemically (EHRHART et al, 1986(EHRHART et al, , 1988HAGN et al, 1986;FISCHER-COLBRIE and SCHOBER, 1987;YOSHIE et al, 1987;BARGSTEN et al, 1988). The tissues under study and reference organs were prepared by identical, established methods (GRUBE and KUSUMOTO, 1986). Throughout all studies, the peroxidase anti-peroxidase (PAP) technique (STERNBERGER, 1986) was applied according to generally standardized protocol (GRUBE and KUSUMOTO, 1986).…”
Section: Concerning the Immunohistochemistrymentioning
confidence: 99%
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“…Serial sections of 0.5 μm thickness were cut from the tissue blocks with an ultramicrotome and mounted on microscope glass slides. After the removal of the resin by sodium methoxide (Grube and Kusumoto, 1986), semithin sections were treated with a 0.05% citraconic anhydride solution (Immunosaver; Nissin EM Co., Ltd., Tokyo, Japan) for 30 min at 60°C as an antigen retrieval procedure (Namimatsu et al, 2005), and then incubated with 2% normal donkey serum (30 min, 20°C) for blocking. After these pretreatments, tissue sections were incubated with a mixture of primary antibodies of different species (rabbit-, mouse-, sheep-/goat-origin) for 16 h at 20°C.…”
Section: Immunofluorescence Microscopymentioning
confidence: 99%