Epoxy embedments sandwiched between ACLAR^® sheets

ACLAR^® pulled away from the flat specimen embedment.

Cut out the area of interest ａnd glue it on a 00 cylinder for sectioning.

For comparative TEM ａnd SEM procedures, cut an ACLAR^® circle in half ａnd compare the two after fixation （Kingsley3）; use a blunt needle to mark.

Fresh material is cut on a vibratory slicer, treated with HRP ａnd placed on ACLAR^® cut into a slide shape - observe under LM - if OK, process for TEM on the slide.

The 1968 paper1 by E. B. Masurovsky ａnd R.P. Bunge was the first to describe ａnd clearly demonstrate the useful chemical ａnd physical properties of ACLAR^® for both tissue culture ａnd electron microscopic purposes. It was first used in the space program ａnd its properties were found to be interesting for biomedical research （personal communication, Dr. E. Masurovsky）. Subsequent work by others developed ACLAR^® applications; attention is brought to that done by Mawe, et al 2, ａnd the comprehensive ACLAR^® study by Kingsley ａnd Cole3.

ACLAR^® overcomes a number of problems regarding the processing of tissue culture cells, epoxy embedments, sectioning ａnd observations because of its chemical inertness, non-stick property, glass clarity, flexibility ａnd smooth surface. It may be cut with scissors or blades ａnd does not damage microtomy knives. It is unsurpassed in moisture barrier protection, transparent to UV ａnd is plasticizer ａnd stabilizer free. It is nonflammable, nonaging ａnd has a low dielectric constant ａnd dissipation. It is high in dielectric strength. ACLAR^® can be sterilized.

• Separates easily from epoxy
• Transparent fluorinated-chlorinated thermoplastic which contains no volatile components
• Chemically inert, for all practical purposes, ideal for growing cell cultures
• Cells adhere to it readily ａnd remain attached after fixation, dehydration ａnd critical point drying or embedding
• Accepts heavy metal sputter coating
• Stable in the scanning electron microscope; melting point 202°C
• ACLAR^® is as transparent as glass
• Fluorescence microscopy possible since ACLAR^® exhibits no detectable autofluorescence
• Can be sectioned ａnd does not damage ultramicrotomy knives
• Considerably simplifies the preparation of cultured cells for all types of microscopy
• sterilizable
• Gives flat sections
• Soft, can be sectioned
• Smooth surface makes light microscopy observations possible
• Does not degrade under UV or gamma ray radiation
• Used as an O2 barrier when flat embedding methacrylate or acrylic resins

ACLAR^® is offered in sheet form, 8 x 12.5" （203 x 318mm） with 7.8 mil （0.2mm） thickness.

References, ACLAR^® Film

1. Masurovsky EB, Bunge RP: Fluoroplastic coverslips for long-term nerve tissue culture. Stain Technology, 43, 3, 161-165 （1968）

2. Mawe GM, Bresnahan JC, Beattie, MS: Ultrastructure of HRP-labelled neurons: a comparison of two sensitive techniques. Brain Research Bulletin, 10, 551 （1983）

3. Kingsley RE, Cole NL: Preparation of cultured mammalian cells for transmission ａnd scanning electron microscopy using Aclar film. J of Electron Microscopy Technique, 10, 77-85 （1988）

ACLAR^® Embedding Film
Physical & Chemical Resistance Data