Microautoradiography of water-soluble compounds in plant tissue after freeze-drying and pressure infiltration with epoxy resin.
Identifieur interne : 004E33 ( Main/Exploration ); précédent : 004E32; suivant : 004E34Microautoradiography of water-soluble compounds in plant tissue after freeze-drying and pressure infiltration with epoxy resin.
Auteurs : T C Vogelmann [États-Unis] ; R E DicksonSource :
- Plant physiology [ 0032-0889 ] ; 1982.
Abstract
It is difficult to retain and localize radioactive, water-soluble compounds within plant cells. Existing techniques retain water-soluble compounds with varying rates of efficiency and are limited to processing only a few samples at one time. We developed a modified pressure infiltration technique for the preparation of microautoradiographs of (14)C-labeled, water-soluble compounds in plant tissue. Samples from cottonwood (Populus deltoides Bartr. ex Marsh.) labeled with (14)C were excised, quick frozen in liquid N(2), freeze-dried at -50 degrees C, and pressure-infiltrated with epoxy resin without intermediate solvents or prolonged incubation times. The technique facilitates the mass processing of samples for microautoradiography, gives good cellular retention of labeled water-soluble compounds, and is highly reproducible.
DOI: 10.1104/pp.70.2.606
PubMed: 16662542
PubMed Central: PMC1067196
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">It is difficult to retain and localize radioactive, water-soluble compounds within plant cells. Existing techniques retain water-soluble compounds with varying rates of efficiency and are limited to processing only a few samples at one time. We developed a modified pressure infiltration technique for the preparation of microautoradiographs of (14)C-labeled, water-soluble compounds in plant tissue. Samples from cottonwood (Populus deltoides Bartr. ex Marsh.) labeled with (14)C were excised, quick frozen in liquid N(2), freeze-dried at -50 degrees C, and pressure-infiltrated with epoxy resin without intermediate solvents or prolonged incubation times. The technique facilitates the mass processing of samples for microautoradiography, gives good cellular retention of labeled water-soluble compounds, and is highly reproducible.</div>
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<Abstract><AbstractText>It is difficult to retain and localize radioactive, water-soluble compounds within plant cells. Existing techniques retain water-soluble compounds with varying rates of efficiency and are limited to processing only a few samples at one time. We developed a modified pressure infiltration technique for the preparation of microautoradiographs of (14)C-labeled, water-soluble compounds in plant tissue. Samples from cottonwood (Populus deltoides Bartr. ex Marsh.) labeled with (14)C were excised, quick frozen in liquid N(2), freeze-dried at -50 degrees C, and pressure-infiltrated with epoxy resin without intermediate solvents or prolonged incubation times. The technique facilitates the mass processing of samples for microautoradiography, gives good cellular retention of labeled water-soluble compounds, and is highly reproducible.</AbstractText>
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<ReferenceList><Reference><Citation>J Ultrastruct Res. 1969 Jan;26(1):31-43</Citation>
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<Reference><Citation>Plant Physiol. 1972 Feb;49(2):161-5</Citation>
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<Reference><Citation>Plant Physiol. 1972 Feb;49(2):166-71</Citation>
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<Reference><Citation>Plant Physiol. 1975 Aug;56(2):185-93</Citation>
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