Results 241 to 250 of about 109,391 (304)

Integrated Histology and Molecular Profiling of Postmortem Human Auditory and Vestibular Organs via a Poly (Methyl Methacrylate)-Based Workflow. [PDF]

open access: yesJ Assoc Res Otolaryngol
Bächinger D   +19 more
europepmc   +1 more source

Advances in multiscale myelin imaging: from classical histology to functional insights. [PDF]

open access: yesFront Cell Neurosci
Okuyama K   +13 more
europepmc   +1 more source

Histo-LOOP: A Novel Embedding Tool for Standardizing, Simplifying, and Advancing Histological Tissue Preparation. [PDF]

open access: yesJ Histochem Cytochem
Nilcham P   +7 more
europepmc   +1 more source

Chemical Dehydration for Rapid Paraffin Embedding

Biotechnic and Histochemistry, 1994
We describe chemical dehydration with 2,2-dimethoxypropane (DMP) for rapid paraffin embedding using a mixture of DMP and mineral oil followed by mineral oil as clearing intermediates. This method is useful for classical histological techniques as well as for histochemistry and immunocytochemistry.
Gabriele Möller
exaly   +3 more sources

Decalcifying Tissues for Paraffin Embedding

Cold Spring Harbor Protocols, 2008
INTRODUCTIONParaffin sections of bone usually require a decalcification step after fixation before sectioning. This protocol describes a method for decalcifying fixed tissue.
Fischer, Andrew H.   +3 more
openaire   +2 more sources

Improvement of the Butyl Methacrylate-Paraffin Embedment

Stain Technology, 1983
The excellent butyl methacrylate-paraffin method as an embedment for light microscopy has been technically improved. More uniform and reproducible polymerization has been obtained by using a vacuum oven to degas the polymerizing mixture and to replace the air with nitrogen at 650 Torr. The amount of benzoyl peroxide required must be determined for each
P J, McMillan   +3 more
openaire   +2 more sources

A Sample-Grouping Technique for Paraffin Embedments

Stain Technology, 1983
A technique is described which facilitates histological preparation of multiple tissue specimens for light microscopy. The procedure enables the investigator to separate and label identifiable subgroups from a larger number of specimens in one histological section. After standard fixation, murine esophagi were arranged longitudinally and secured within
N H, Rubin, P S, Baur
openaire   +2 more sources

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