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Model 3d

Manufactured by Newport Scientific
Sourced in Australia

The Model 3D is a versatile laboratory equipment designed for performing various analytical and experimental tasks. It features a compact and durable construction, ensuring reliable performance in a wide range of scientific applications. The core function of the Model 3D is to provide a controlled and precise environment for conducting experiments and analyses.

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7 protocols using model 3d

1

Evaluating Maize Starch Pasting Properties

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The pasting properties of maize starch were evaluated using RVA (Model 3D, Newport Scientific, Sydney, NSW, Australia). Three grams of starch obtained from each line was mixed with 25 ml of distilled water in the RVA canister. The RVA profile took a heat–hold–cool temperature cycle as follows: (1) set at 50°C as the starting temperature and maintained for 1 min; (2) heated to 95°C and held at 95°C for 2.5 min; and (3) cooled to 50°C and kept at 50°C for 1.4 min. The total processing time was about 12 min. The pasting properties were determined using a fixed paddle rotation at the speed of 160 r/m. The RVA parameters were recorded in centipose (cP). The pasting parameters obtained from the pasting curve including PV, TV, FV, PTP, PT and their derived parameters, BD and SB were recorded for all the inbred lines. The average value of three biological replicates from each line was obtained for data analysis.
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2

Analyzing Starch Pasting Behavior

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The pasting properties of starch were determined using RVA (Model 3D, Newport Scientific, Australia) according to the method previously reported [56 ]. 3 g starch and 25 g ultrapure water were mixed in an aluminum crucible and tested on the machine. Starch samples were heated from 50 °C to 95 °C at 12 °C/min, maintained at 95 °C for 2.5 min, cooled to 50 °C at 12 °C/min and finally held at 50 °C for 1.4 min. The rotor speed is 160 r/min. Each sample measured three replicates.
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3

Starch Rheology and Thermal Analysis

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The starch rapid viscosity analyzer (RVA) profiles were carried out by rapid viscosity analyzer (Model 3D, Newport Scientific, Warriewood, Australia) and thermal properties were performed in a DSC8500 equipped with a refrigerated cooling system (Perkin Elmer, Diamond, AR, USA).
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4

Rapid Viscosity Analysis of Rice Starch

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Pasting properties of rice starch were measured by a rapid viscosity analyzer (Model 3D, Newport Scientific, Australia) with Thermocline for Windows software (version 2.0). Rice flour (3 g each sample) was mixed with 25 ml of distilled water in an aluminum RVA canister. A programmed heating and cooling cycle were set as described by Zhong et al. (2005) (link). The starch sample was held at 50°C for 1 min, heated from 50 to 95°C at 12°C/min, held at 95°C for 2.5 min, cooled to 50°C at 12°C/min, and held at 50°C for 2.5 min. All measurements were two times replicated. The peak viscosity (PKV), hot paste viscosity (HPV), cold paste viscosity (CPV), and their derivative parameters, including breakdown (BD = PV-HPV) and setback (SB = CPV-PV), were recorded. Triplicate measurements were taken for each sample.
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5

Starch Pasting Properties Analysis

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Starch pasting properties were determined using a rapid viscosity analyzer (Model 3D, Newport Scientific, Warriewood, NSW, Australia). Starch samples were 2.5 g total weight; 7%, w/w, dry basis and mixed with 25 g H2O. The programming cycle for pasting was set at 14 min. Starch samples were started at 50 °C for 1 min and then heated from 50 °C to 95 °C, held at 95 °C for 2.5 min, cooled to 50 °C at 12 min and finally held for 2 min [4 (link)].
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6

Comprehensive Rice Quality Analysis

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The grains were air-dried and stored for three months, the gel consistency, amylose content and amylopectin content were determined with reference to (GB/T17891-2017 High-Quality Rice Grain). The protein and its components content of grains were measured with milled rice as the test sample using an automatic Kjeldahl apparatus, wherein the protein components were measured according to the method of Tang, (1999) , the albumin was extracted with distilled water, globulin was extracted with 0.06 mol L-1 NaCl solution, prolamin was extracted with 75% ethanol solution, and glutenin was extracted with 0.04 mol L-1 NaOH solution, and the above extracts were tested to determine the protein components content.
The cooking and eating quality were measured by using the Japanese cooking rice taste meter STA1B to determine the rice characteristics and its related taste properties with Heilongjiang japonica rice in China as the reference standard. The RVA spectral characteristic value (RVA value) was measured with 3 g of a 100-mesh sieved rice flour sample, plus 25 g of ultrapure water, using a rapid viscosity analyzer (Model 3D, Newport Scientific, Australia) according to AACC (American Association of Cereal Chemists) procedure for rapid determination, and its supporting software TWC (Thermal cycle for windows) was used for data analysis.
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7

Starch Pasting and Thermal Properties

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The starch pasting properties were tested using a rapid viscosity analyzer (RVA) (Model 3D, Newport Scientific, Warriewood, Australia) according to the method of Lu and Lu [32 (link)]. Briefly, rice flour at a concentration of 12% (w/w) was mixed at a constant stir speed of 160 g using the standard profile. The temperature profile employed was as follows: the start temperature was 50 °C held for 1 min, followed by heating to 95 °C at 11.84 °C/min, held at 95 °C for 2.5 min, and then cooling at the same speed to 50 °C and held for 1 min.
The thermal properties were investigated by a differential scanning calorimetry (DSC) with a Model 200 F3 Maia (Netzsch, Selb, Germany). Using an empty aluminum pan as a reference, the ratio of the weight of starch to water was 1:3 for each sample, which was sealed in a hermetic aluminum pan and scanned from 30 to 95 °C at a heating rate of 10 °C/min after overnight equilibration at room temperature [33 (link)]. The thermal transitions of starch samples were defined as To (onset temperature), Tp (peak of gelatinization temperature), and Tc (conclusion temperature), and ΔH referred to the enthalpy of gelatinization.
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