2006
DOI: 10.1002/bem.20192
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A small temperature rise may contribute towards the apparent induction by microwaves of heat-shock gene expression in the nematodeCaenorhabditis Elegans

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Cited by 41 publications
(61 citation statements)
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“…Cultures of PC72 worms were synchronised by filtration through a 5 m mesh filter [Mutwakil et al, 1997], and L1 larvae recovered from the filtrate were grown on 9 cm NGM agar plates [Sulston & Hodgkin, 1988] at 15C until they reached the L4/young adult stage. They were then washed off the plates with ice-cold K medium (53 mM NaCl, 32 mM KCl) [Williams & Dusenbery, 1990] and allowed to settle twice on ice for about 10 min to remove excess bacteria [Dawe et al, 2006]. Equal aliquots of 2-3000 worms were added to 2 ml of fresh K medium in each of the twelve 3.5 cm Petri dishes, which were divided between two 6-dish holders, labelled according to position, and placed inside the upper or lower chambers of the exposure rig.…”
Section: Worm Culture and Processingmentioning
confidence: 99%
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“…Cultures of PC72 worms were synchronised by filtration through a 5 m mesh filter [Mutwakil et al, 1997], and L1 larvae recovered from the filtrate were grown on 9 cm NGM agar plates [Sulston & Hodgkin, 1988] at 15C until they reached the L4/young adult stage. They were then washed off the plates with ice-cold K medium (53 mM NaCl, 32 mM KCl) [Williams & Dusenbery, 1990] and allowed to settle twice on ice for about 10 min to remove excess bacteria [Dawe et al, 2006]. Equal aliquots of 2-3000 worms were added to 2 ml of fresh K medium in each of the twelve 3.5 cm Petri dishes, which were divided between two 6-dish holders, labelled according to position, and placed inside the upper or lower chambers of the exposure rig.…”
Section: Worm Culture and Processingmentioning
confidence: 99%
“…After exposure, worms were immediately spun down (500 x g for 2 min) and the pellets snap frozen on solid CO 2 ; all of the frozen worm samples were sent back to Nottingham in an insulated container of solid CO 2 for subsequent reporter analysis, and all remained frozen on arrival. The activity of the PC72 hsp16-1::lacZ reporter gene (encoding -galactosidase) was measured on thawed worm samples using the standard MUG assay (with 4-methylumbelliferyl-D-galactopyranoside as substrate), exactly as described previously [Dawe et al, 2006]. Because the P90C food bacteria are deleted for the lacoperon, all -galactosidase activity detected must originate from the lacZ transgene carried by the PC72 worms.…”
Section: Worm Culture and Processingmentioning
confidence: 99%
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