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Amylose amylopectin kit

Manufactured by Megazyme
Sourced in Ireland

The Amylose/amylopectin kit is a laboratory tool used to quantify the relative amounts of amylose and amylopectin in starch samples. It provides a method for the determination of these two polysaccharide components.

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4 protocols using amylose amylopectin kit

1

Green Banana Flour Characterization

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Flour from five green banana cultivars, namely Grande Naine, Pisang Awak, Finger Rose, FHIA-01 and Du Roi, was kindly provided by the Agricultural Research Counsel (ARC) Tropical and Subtropical Crops, Nelspruit, Mbombela in South African. All reagents were analytical grade, Trolox, Folin–Ciocalteu reagent, gallic acid and quercetin were purchased from Sigma-Aldrich Pty. Ltd. (Johannesburg, South Africa). The resistant starch assay kit and the amylose/amylopectin kit were purchased from Megazyme Ltd. (Johannesburg, South Africa).
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2

Dietary Fiber Composition Analysis

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Soluble and insoluble dietary fiber contents were measured according to an enzymatic gravimetric method.20 The neutral sugars of the isolated dietary fiber residues and fecal material were analyzed using a gas‐chromatographic method,21 and arabinoxylan content was estimated as the sum of arabinose and xylose in the fiber residues. The degree of fermentation was calculated as in Equation (1), during the five days of the experimental period.
1 grams of neutral sugars in faeces / grams of neutral sugars consumed ×100
The content of β‐glucan was assessed with the mixed‐linkage β‐glucan assay kit (K‐BGLU, Megazyme International, Ireland). The average β‐glucan Mw of extractable β‐glucans was estimated with high‐performance size exclusion chromatography and fluorescence detection (HPSEC–FD) with Calcofluor post‐column complexation.22 Resistant starch was estimated by the difference between total and available starch, obtained by an enzymatic assay with KOH and/or digestion with α‐amylase and amyloglucosidase.23, 24 The amylose content was quantified with an amylose/amylopectin kit (Megazyme International, Ireland). The crude protein was quantified with an elemental analyzer (Flash EA 1112, Thermo Fisher Scientific Inc., Waltham, MA, USA). All analyses were made at least in duplicate.
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3

Comprehensive Food Composition Analysis

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The contents of moisture, crude protein (GB 5009.5-2016), crude fat (GB 5009.6-2016), and ash (GB 5009.4-2016) were determined according to the National Standards of China. The contents of total starch, amylose, and damaged starch were determined using a Total Starch Assay Kit, Amylose/Amylopectin Kit, and Starch Damage Assay Kit (Megazyme International Ltd., Wicklow, Ireland), respectively.
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4

Pollen Viability and Grain Traits of OsOr Transgenic Rice

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Pollen viability was evaluated as previously described [25 (link)] from transgenic plants with OsOr gene and wild-type plants at flowering time for pollen germination analysis. Nikon SMZ800N microscope (Nikon Metrology Inc., Seoul, Korea) was used to observe pollen germination. The amylose content of whole grain was measured using the AMYLOSE/AMYLOPECTIN kit (Megazyme Ltd., Bray, Ireland) according to the manual provided by the manufacturer. The morphology of starch grains was observed by scanning electron microscopy (SEM). Images were captured using a Quanta FEG 450 instrument (ZFE, Graz, Austria). Xanthomonas oryzae pv. oryzae (Xoo) inoculation and determination of bacterial populations were evaluated as previously described [26 (link),27 (link)] for a wild-type plant and transgenic plants. In addition, 30 plants were randomly selected from each of the transgenic lines and NT plants, and the seed setting rate, pollen fertility, 1000-grain weight, and yield per plant were investigated.
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