Literature DB >> 3546700

Temperature control in Lowicryl K4M and glycol methacrylate during polymerization: is there a low-temperature embedding method?

A E Ashford, W G Allaway, F Gubler, A Lennon, J Sleegers.   

Abstract

An apparatus for embedding tissues at resin temperatures down to 228 K is described. By placing thermocouples in the resin the temperature has been monitored during embedding at low temperature with glycol methacrylate (GMA) and Lowicryl K4M. Even in this apparatus with a liquid cooling bath the heat of polymerization is not dissipated and the resin temperature rises. This rise is directly proportional to the resin temperature at the onset of polymerization and is higher in Lowicryl K4M than GMA. The initial resin temperature also affects the time taken for polymerization. The time to the onset of the peak and its duration are both increased as the temperature is lowered. This effect is more pronounced with GMA than Lowicryl K4M and polymerization of GMA is inhibited at the lowest temperature used. When Lowicryl K4M, polymerized at low temperature, is warmed up to ambient a further exothermic reaction occurs, which causes the resin temperature to rise well above ambient. Both this temperature peak and that during polymerization are reduced, but not totally eliminated, by reducing the resin volume. Air-cooled systems are inefficient compared with the low-temperature apparatus used here and the resin temperature rise is consequently greater and, even with small resin volumes, it can be very high. It is therefore unlikely for published methods that the temperature specified has been maintained in the resin during polymerization. The implications of these findings are discussed in relation to enzyme and antigen survival. Recommendations include use of very small volumes of resin, refrigerated liquid-bath rather than air-cooled systems and contact with a heat sink when specimens are warmed up to ambient temperature. Examples of enzyme reaction, antigen survival and structural preservation obtained with the method are presented.

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Year:  1986        PMID: 3546700     DOI: 10.1111/j.1365-2818.1986.tb02793.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  7 in total

1.  Involvement of the Golgi apparatus in the secretion of α-amylase from gibberellin-treated barley aleurone cells.

Authors:  F Gubler; J V Jacobsen; A E Ashford
Journal:  Planta       Date:  1986-09       Impact factor: 4.116

2.  Improvements in immunostaining samples embedded in methacrylate: localization of microtubules and other antigens throughout developing organs in plants of diverse taxa.

Authors:  T I Baskin; C H Busby; L C Fowke; M Sammut; F Gubler
Journal:  Planta       Date:  1992-06       Impact factor: 4.116

3.  Applicability of using acrylic resins in post-embedding ultrastructural immunolabelling of human neutrophil granule proteins.

Authors:  H C Mutasa
Journal:  Histochem J       Date:  1989-05

4.  Preparation of plant cells for transmission electron microscopy to optimize immunogold labeling of carbohydrate and protein epitopes.

Authors:  Sarah M Wilson; Antony Bacic
Journal:  Nat Protoc       Date:  2012-08-23       Impact factor: 13.491

5.  Electron microscopic immunocytochemical localization of proline-rich proteins in normal mouse parotid salivary glands.

Authors:  H Mansouri; G H Cope; N Divecha; C J McDonald
Journal:  Histochem J       Date:  1992-10

6.  The release of α-amylase through gibberellin-treated barley aleurone cell walls : An immunocytochemical study with Lowicryl K4M.

Authors:  F Gubler; A E Ashford; J V Jacobsen
Journal:  Planta       Date:  1987-10       Impact factor: 4.116

7.  The organization of myosin and actin in rapid frozen nerve growth cones.

Authors:  P C Bridgman; M E Dailey
Journal:  J Cell Biol       Date:  1989-01       Impact factor: 10.539

  7 in total

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