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Paraffin wax

Manufactured by Leica Microsystems
Sourced in Germany

Paraffin wax is a versatile material used in various laboratory applications. It is a solid, waxy substance derived from petroleum, coal, or shale oil. Paraffin wax has a high melting point and is commonly used as a embedding medium for tissue samples in histological and pathological analyses.

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3 protocols using paraffin wax

1

Preparation of Paraffin Embedding Blocks

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Paraffin wax was purchased from Leica Microsystems, Inc. (Wetzlar, Germany).
Blank paraffin blocks prepared for the recipient blocks were made according to
routine procedures. Briefly, ordinary stainless-steel embedding molds and
plastic cassettes were placed in melted paraffin and warmed to 62°C before
filling to avoid the formation of bubbles in the paraffin blocks. The mold was
then filled with melted paraffin and covered with a plastic cassette. After
pouring, the paraffin blocks were cooled to room temperature and removed from
the steel molds. These blank paraffin blocks were examined, and those without
air bubbles and cracks were selected for to prepare the recipient block. The
paraffin block with a plastic cassette was placed at the bottom of the plastic
mold to fix the paraffin block and avoid its displacement during drilling. Holes
were created in the recipient block using a mini-drill. The recipient block was
removed after drilling was completed.
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2

Brain Tissue Processing for Histological Analysis

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Brian tissues samples including cerebellum, cerebrum, and hippocampus were collected and fixed in 10% neutral buffered formalin solution and given overnight washings under tap water. Dehydration of samples was done through ascending grades of alcohol (70%, 80%, 90%, and absolute alcohol) followed by clearing with acetone. Tissues were embedded in paraffin wax (Leica Microsystem) for further processing. Approximately, 4-5 µ thick sections were cut, stained with routine hematoxylin and eosin (H and E) staining technique [10 ] and examined by BX61 Research Photomicrograph Microscope System (Olympus Corporation, USA), the facility provided by the department.
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3

Tissue Processing and Staining of Tasmanian Devil Samples

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Tasmanian devil tissues were fixed in 10% Neutral Buffered Formaldehyde (Australian Biostain, Traralgon, VIC, Australia) for 24 hr and selected tissues were cassetted (Techno Plas, St. Marys, SA, Australia) and processed overnight using a standard 15-hr overnight procedure in the TP 1050 tissue processor (Leica Microsystems, Wetzlar, Germany). Tissues were orientated on the EG1160 (Leica Microsystems), embedded in paraffin wax (Leica Microsystems) and sectioned at 3 microns using a Leica RM2245 microtome and adhered to microscope slides (Menzel Gläser, Thermo Fisher Scientific) for 20 min at 60°C. Sections were deparaffinized, rehydrated and stained using Jung autostainer XL (Leica Microsystems) for Hematoxylin (Australian Biostain) and Eosin, dehydrated, cleared, cover slipped (Leica Microsystems) and mounted in CV Mount (Leica Microsystems) (Hayes et al., 2017 (link)).
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