1997
DOI: 10.1006/fstl.1997.0262
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A New Method for Determining the Area of Cell Walls in Rye Doughs Based on Fluorescence Microscopy and Computer-assisted Image Analysis

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Cited by 15 publications
(4 citation statements)
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“…The total area calculated was 40 mm2. The surface area of insoluble cell walls was studied using computerised image analysis (Cue-2) and Ñuorescence microscopy (Olympus, Vanox T, Japan) (Parkkonen et al 1997).…”
Section: Analysesmentioning
confidence: 99%
“…The total area calculated was 40 mm2. The surface area of insoluble cell walls was studied using computerised image analysis (Cue-2) and Ñuorescence microscopy (Olympus, Vanox T, Japan) (Parkkonen et al 1997).…”
Section: Analysesmentioning
confidence: 99%
“…Grains were humidified for 16 h at 4 °C and fixed in 20 mL L −1 gluteraldehyde in 0.1 mol L −1 phosphate buffer (pH 7.0) for 4 h at 20 °C, washed in water five times for 10 min. Cross-sections, 60 μm thick, were cut with a vibratome (Microcut H1200) and stained with Nile Red (Nile Blue A Oxazone) and Calcofluor White M2R (Fluorescent Brightener 28), counterstained by Fast Green as described by Martelli et al . Stains were purchased from Sigma-Aldrich Co. (USA).…”
Section: Methodsmentioning
confidence: 99%
“…Sections were cut 4 pm thick in a Leica rotary microtome HM 355 (Heidelberg, Germany) using a steel knife. The sections were transferred onto glass slides and stained with Light Green and Lugol's iodine solution (Fulcher and Wong 1980;Wood et al 1983;Parkkonen et al 1994). Protein was stained with aqueous 0.1 % (w/v) Light Green for 1 min (Gun, BDH Ltd, Poole, UK) and starch with 1:lO diluted Lugol's iodine solution (I, 0.33 $4, w/v and KI 0.67%, wh).…”
Section: Microscopy and Image Analysismentioning
confidence: 99%