2000
DOI: 10.1006/abio.2000.4852
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A Fast and Inexpensive Procedure for Drying Polyacrylamide Gels

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Cited by 7 publications
(6 citation statements)
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“…To understand the reversible swelling mechanism of polyacrylamide-bisacrylamide hydrogels in ethanol, it is important to know why these hydrogels have a sensitivity to ethanol. Fadouloglou et al used ethanol to dry out polyacrylamide hydrogels, which are the standard system for gel electrophoresis of proteins, reproducibly after electrophoresis and observed a uniform shrinking of the gel after 20 min in 95 vol% ethanol (Fadouloglou et al, 2000). However, the authors have not given any explanation for this effect.…”
Section: Reversibility Of Hydrogel Swellingmentioning
confidence: 99%
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“…To understand the reversible swelling mechanism of polyacrylamide-bisacrylamide hydrogels in ethanol, it is important to know why these hydrogels have a sensitivity to ethanol. Fadouloglou et al used ethanol to dry out polyacrylamide hydrogels, which are the standard system for gel electrophoresis of proteins, reproducibly after electrophoresis and observed a uniform shrinking of the gel after 20 min in 95 vol% ethanol (Fadouloglou et al, 2000). However, the authors have not given any explanation for this effect.…”
Section: Reversibility Of Hydrogel Swellingmentioning
confidence: 99%
“…As expected, the response time of the sensors amounting to a few minutes is shorter than of hydrogels in free-swelling mode. The response times of the sensors could be further reduced by using porous hydrogels (Franke et al, 2017).…”
Section: Piezoresistive Ethanol Sensormentioning
confidence: 99%
“…14,15) Briefly, after treatment with asiatic acid, SW480 cells were lysed and suspended in Trisethylenediaminetetraacetic acid (EDTA) buffer (pH 7.5). Precipitation solution was added, mixed and each sample was placed on ice for 15 min.…”
Section: Asiatic Acid Induces Colon Cancer Cell Growth Inhibition Andmentioning
confidence: 99%
“…Reduced and denatured samples were loaded onto NuPAGE s Novex s 4-12% Bis-Tris polyacrylamide gels (Life Technologies) and electrophoresed at constant voltage in 1 Â Novex s 2-(N-morpholino)ethanesulfonic acid running buffer (MES; 145 V) (Life Technologies) or 1 Â Novex s 3-(N-morpholino)propanesulfonic acid running buffer (MOPS; 125 V) (Life Technologies) supplemented with NuPAGE s antioxidant (Life Technologies) per manufacturer's instructions. PAGE separated gels were incubated in gel drying buffer [50% methanol (HPLC grade; Honeywell), 7.5% glacial acetic acid (Fisher Chemical), and 10% glycerol (ACS grade; Macron)] for 30 min at room temperature (RT), further dehydrated in 200 proof ethanol (ETOH, Decon Laboratories) for 15 min at RT (Fadouloglou et al, 2000), and then submerged in Amersham™ Amplify™ fluorographic reagent (GE Healthcare) for 30 min at RT to infuse the gel with the fluorographic reagent. PAGE gels were dried completely under vacuum at 80 1C for 2 h. PAGE separated [35] Scysteine labeled products were imaged using BIOMAX MR HighResolution Film (Carestream).…”
Section: Polyacrylamide Gel Electrophoresismentioning
confidence: 99%