1. |
Enhancement of Histological Detail Using Metanil Yellow as Counterstain in Periodic Acid Schiff's Hematoxylin Staining of Glycol Methacrylate Tissue Sections |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 169-172
QuinteroIliana,
GrierHarry,
MuscatoMarilou,
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摘要:
Histological detail in sections from tissues embedded in glycol methacrylate was improved by counterstaining PAS/iron-hematoxylin stained sections with a dilute solution of metanil yellow. The addition of the counterstain increases contrast in tissue sections and highlights PAS-positive entities. The staining protocol provides sharp definition of tissue morphology, differentiates cell types and other tissue components and does not produce background staining.
ISSN:1052-0295
DOI:10.3109/10520299109109964
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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2. |
Preservation of Tracheal Mucus by Nonaqueous Fixative |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 173-180
SimsDavid E.,
WestfallJane A.,
KiorpesAnthony L.,
HomeMargaret M.,
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摘要:
Two nonaqueous fixatives, composed of fluorocarbon solvents with dissolved osmium tetroxide, were used to determine the feasibility of preserving the mucous coat in bovine and rat trachea for light and electron microscopy. Aqueous fixatives, while providing excellent cytological preservation, wash away the mucous lining, precluding ultrastructural analysis. Inclusion of ruthenium red or alcian blue within aqueous fixative improved retention of mucus, but provided incomplete, patchy results. Fixation with nonaqueous fluorocarbon solvent and dissolved osmium tetroxide preserved a continuous mucous epiphase layer above a clear hypophase layer. Subcomponents of the mucus included an electron dense surface layer, interrupted patches of mucus above the surface layer and electron dense membrane-like material within the mucus. This method of fixation will preserve mucus for light, scanning and transmission electron microscopy, using either intratracheal or immersion methods of fixation. The latter would enable use of materials from large animal models, autopsy or an abattoir.
ISSN:1052-0295
DOI:10.3109/10520299109109965
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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3. |
Application of Stains-All for Demarcation of Cement Lines in Methacrylate Embedded Bone |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 181-184
GruberHelen E.,
MekikianPertchoui,
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摘要:
Cement lines provide a record of sites of past remodeling buried in the matrix of bone. A method is reported for application of Stains-all, a cationic carbocyanine dye, for demarcation of cement lines in bone. The method, which is simple, works well for both glycol methacrylate and methyl methacrylate undemineralized embedments and produces good concomitant staining of cytoplasm and nuclei of osteoblasts, osteoclasts and marrow cells.
ISSN:1052-0295
DOI:10.3109/10520299109109966
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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4. |
Enzyme, Lectin and Immunohistochemistry of Plastic Embedded Undecalcified Bone and other Hard Tissues for Light Microscopic Investigations |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 185-193
HillmannGeorg,
HillmanBeate,
DonathKarl,
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摘要:
Enzymes and tissue antigens were localized on plastic embedded undecalcified bones and teeth using Technovit 7200 VLC (Kulzer, Germany). This resin is hard enough for cutting and grinding procedures on rotating plates with diamond layers. The pores between the diamond grains are not obstructed with this resin. The procedure described here permits localization of antigens in the soft tissues adjacent to, or in the biological hard tissues themselves and in dental implants (ceramic or metallic) on the light microscopic level. The undecalcified bone is fixed and embedded in plastic and cut at 100-150μm. The slices are ground automatically by a grinding machine to a thickness of 5-10μm. After application of the substrates for alkaline and acid phosphatases and the required dyes, the distribution of these enzymes can be demonstrated. Tissue antigens also can be detected with slightly modified standard techniques of immunohistochemistry and lectin histochemistry using the peroxidase technique or fluorescence microscopy.
ISSN:1052-0295
DOI:10.3109/10520299109109967
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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5. |
The Taming of Immunohistochemistry: The New Era of Quality Control |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 194-199
HermanGilbert E.,
ElfontEdna A.,
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摘要:
The most critical factor for interpreting the results of immunohistochemistry is verification of antibody sensitivity and specificity. While some manufacturers supply material data sheets with this information, many do not. This paper describes a well-defined quality assurance program for testing immune reagents. This program can be used to provide commercial suppliers of antisera with analyses of their products destined for government licensure applications. This paper illustrates the protocol and explains the testing philosophy developed over the last eight years.
ISSN:1052-0295
DOI:10.3109/10520299109109968
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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6. |
A New Technique Facilitating Studies of Scant Cell Specimens |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 200-202
DuarteLeeann,
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摘要:
A simple method is described by which multiple cytological and cytochemical studies can be done on a clinical sample that contains relatively few cells. The cells are concentrated by centrifugation. The cell pellet is fixed, frozen and embedded in plastic. Thin (2-μm) sections are cut from the plastic. Thus, each cell may appear in several sections and many slides can be made from a single specimen. The advantages of this method over cytospins and Millipore filter preparations of cell suspensions are optimal utilization of all cells, excellent morphological and immunological preservation and ease and reproducibility of this technique.
ISSN:1052-0295
DOI:10.3109/10520299109109969
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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7. |
Crush and Smear Technique for Rapid Detection and Semiquantitation of Amyloid Deposition |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 203-207
ShtrasburgShmuel,
GalRivka,
PrasMordechai,
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摘要:
A method using Congo red to rapidly identify and semiquantitate amyloid deposits in tissues for experimental research and clinical medicine is described. Examination by polarization microscopy revealed amyloid deposits as bright green birefringent clumps on a dark red background. On semiquantitative evaluation, good correlation was found between this technique and the conventional histological one, the present technique being more sensitive. The method described saves time and expense.
ISSN:1052-0295
DOI:10.3109/10520299109109970
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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8. |
Short Nissl Staining for Incubated Cryostat Sections of the Brain |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 208-209
LindroosO. F.C.,
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摘要:
Nissl stain often binds poorly to cryostat sections which have been incubated in solutions of radiolabeled ligands. Such incubation is used in receptor autoradiography of the brain when using the in vitro method. We have developed a rapid (16 min) modification of Nissl staining for sections that bind stain poroly, e.g., incubated sections. The method stains well sections which cannot be stained with other rapid Nissl staining methods.
ISSN:1052-0295
DOI:10.3109/10520299109109971
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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9. |
In Situ Hybridization ofLiliumWhole Mount Synaptonemal Complex Chromosomal Preparations |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 210-215
HasenkampfClare A.,
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摘要:
Whole mount meiotic preparations of the synaptonemal complex complement ofLiliumhave been used for in situ hybridization experiments. A probe of the maize ribosomal DNA gene cluster has been successfully hybridized to the lily preparations. Three strong signals, corresponding to the three known lily nucleolus organizer regions, have been seen in most of the chromosome preparations. In situ hybridization experiments using meiotic preparations should be useful for identifying specific chromosomes, and for investigating the role of particular DNA molecules important to meiotic function.
ISSN:1052-0295
DOI:10.3109/10520299109109972
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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10. |
A Method to Stain Decalcified Bone without Loss of Structural Detail |
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Biotechnic&Histochemistry,
Volume 66,
Issue 4,
1991,
Page 216-219
SchoenFrances A.,
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摘要:
A modification of Bodian's protargol-S technique is done on 7μm sections of decalcified bone. Light microscopic results are greatly improved when compared to either ground bone sections or decalcified bone stained routinely with hematoxylin and eosin.
ISSN:1052-0295
DOI:10.3109/10520299109109973
出版商:Taylor&Francis
年代:1991
数据来源: Taylor
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