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Mixer b 400

Manufactured by Büchi
Sourced in Switzerland

The Mixer B-400 is a laboratory equipment designed for mixing liquids and powders. It features a stainless steel mixing container and a variable speed motor for adjustable mixing intensity. The core function of the Mixer B-400 is to effectively combine and homogenize samples for various laboratory applications.

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12 protocols using mixer b 400

1

Isolation of Alcohol-Insoluble Residue from Tomatoes

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After thawing, the blanched tomato slices were mixed in a laboratory blender (Waring Commercial, Torrington, CT, USA) two times for three seconds and subsequently filtered over a 1-mm sieve in order to remove peels and seeds [44 (link)]. The AIR was prepared based on the method by McFeeters and Armstrong [45 (link)]. In short, 192 mL technical ethanol was added to 60 g sieved tomato tissue and mixed (Mixer B-400, Büchi, Flawil, Switzerland) three times for six seconds. The precipitated material was recovered by vacuum filtration using filter paper (MN615, Macherey-Nagel, Düren, Germany). Two precipitates were combined, re-dispersed in 192 mL technical ethanol by mixing (Mixer B-400, Büchi, Flawil, Switzerland) three times for six seconds. The precipitate, again recovered by vacuum filtration, was dispersed for 10 min in 192 mL technical acetone by stirring. Next, the acetone was removed by vacuum filtration and the precipitate was dried overnight at 40 °C to obtain dry AIR. After grounding with mortar and pestle, the AIR was kept in a well-closed container until further use.
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2

Organ Collection and Analysis

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Afterwards, the carcass and offal of individual animals were inspected and deemed acceptable for human consumption and the heart, kidneys, tongue, liver, and brain were collected from the slaughterhouse. Musculus semitendinosus and the five above-listed organs were removed from the animals. Each organ was individually labeled, frozen, and transported to the West Pomeranian University of Technology for further analyses. At 48 h post-mortem, samples for chemical analyses were homogenized using a Büchi Mixer B-400 (Büchi Labortechnik, Flawil, AG, Switzerland). Samples were analyzed in duplicate.
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3

Analyzing Moisture and Fat Content in Cakes

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Moisture and fat were detected according to Bostian et al. [36 (link)]. Two samples (30 × 30 mm) from each cake treatment were used for moisture and fat determination. As three independent trials were carried out, results obtained for moisture and fat represent a mean of 6 values (3 × 2 = 6). The Büchi Mixer B-400 (Büchi Labortechnik AG, Switzerland) was used in order to homogenise for compositional analysis. Moisture content was detected on the CEM SMART system and fat content was detected on the SMART Trac system (CEM GmbH, kamp-Lintfort, Germany). Two fibreglass pads were placed in the drying chamber of the CEM SMART system and their weight was tared. The pads were removed and the homogenised samples (2–4 g) were weighed accurately on the pads using separate weighing scales. Following this, one pad was placed over the sample, pressed together and placed back into the drying chamber to begin drying. The moisture (%) was displayed within a few minutes. A sheet of Smart Trac film was used to determine a percent of fats by wrapping the fibreglass pads with the sample. After wrapping, the samples were placed in a tube of the Smart Trac system and positioned in the Smart Trac NMR unit. After about 5 min, the percentage of fat was determined.
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4

Buckwheat Husk Impact on Frankfurter-type Sausages

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The research material consisted of frankfurter-type sausages differing in the proportion of buckwheat husk (BH) in the formulation (Table 1). For this purpose, ham cuts (M. semimembranosus) and backfat were obtained from Dworecki Meat Processing Plant (Golejewo, Poland) 48 h post-mortem. Raw materials were passed through a meat grinder (Zelmer, fi 6), then 200 g of meat and 120 g of fat were mixed with ice, curing salt (4.8 g, Żuk-Pol, Wrocław, Poland), sugar, seasoning (Bellako sp. z o.o., Zabrze, Poland) and the appropriate amount of ground buckwheat husk (0% BH = 0 g, 1% BH = 4 g, 2% BH = 8 g and 3% BH = 12 g, respectively, Młyn Niedźwiady, Kalisz, Poland). The mixture was homogenized for 3 sec at 9000 rpm with a Büchi Mixer B400 (BÜCHI Labortechnik GmbH, Flawil, Germany). The homogenized mass was weighed (approximately 60 g) in polypropylene tubes (2.5 × 12 cm) and then heat treated in a water bath (99 °C, Julabo TW12, Julabo Inc., Allentown, PA, USA) until a temperature of 72 °C was reached at the geometric center of sample. Once this temperature was reached, the product was cooled on ice. The cooled products were vacuum packed in multilayer PA/PE bags and stored at 4 ± 2 °C for further analyses. The sausages were manufactured in two production batches on different days.
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5

Standardized Potato Frying Protocol

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For the strips fried in a fryer, an electric fryer (Hendi Blue Line, Rhenen, The Netherlands) made of stainless steel, with a capacity of 4 L and equipped with 2 detachable frying pans with an element warning light with a heating and safety thermostat to prevent overheating was used. Palm oil was used to fry the potatoes, using a 4:1 oil/potato ratio (w/w) (2536 g oil and 634 g potatoes). The frying temperature was adjusted to 190 °C and was monitored during frying, using the same digital thermometer. The frying time of the potato strips was 11 min.
Potato strips were placed on absorbent paper after frying. The experiments were performed in duplicate, using fresh oil, without reusing the oil in any experiment.
After frying, French fries were ground in a Büchi mixer (B-400, BÜCHI Labortechnik AG, Flawil, Switzerland) and stored at −25 °C until further analysis.
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6

Chocolate Brownie Composition Analysis

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Two chocolate brownies (45x45mm) from each independent trial (three) were used for moisture and fat determination (3 x 2 = 6). Samples were homogenised for compositional analysis using Büchi Mixer B-400 (Büchi Labortechnik AG, Switzerland). Moisture content was determined using the CEM SMART system and fat was determined using the SMART Trac system (CEM GmbH, kamp-Lintfort, Germany). Two fibreglass pads were placed in the
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7

Meat Quality Evaluation Protocol

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The analysis of physical traits included measuring the offal for the concentration of hydrogen ions 45 min and 24 h postmortem with a pH-Star CPU device (Matthäus), which is used in the meat plant in which the animals were slaughtered. Moreover, the percentage of free water (WHC—water holding capacity) was determined by the method of Grau and Hamm [18 ] modified by Pohja and Niinivaara [19 ].
The offal samples were homogenized 48 h postmortem using a Büchi Mixer B-400 (Flawil, Switzerland) and analysed for the percentage of water, total protein, collagen, and total fat. This was done with a FoodScanTM meat analyser (Foos) using near-infrared spectrometry (NIR) according to standard PN-A-82109 [20 ].
The energy value (kJ per 100 g−1 of fresh tissue) of each offal was calculated from the total protein and fat percentage. The calculations were based on Atwater equivalents, where: 1 g protein = 4.0 kcal = 16.76 kJ; 1 g fat = 9.0 kcal = 37.66 kJ.
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8

Mycotoxin Screening in Sicilian Maize and Pepper

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The method was applied to screen mycotoxins in Sicily (Southern Italy). About 10 kg of maize and 5 kg of black pepper were collected from 2 different local vendors in Palermo (Sicily) and used for validation procedures. Samples were grounded using a Mixer B-400 laboratory mill by BÜCHI (Cornaredo, Italy) at ambient temperature with knives’ rotation speed of 9000 rpm. Samples grounded were stored at −10 °C until analysis.
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9

Organic Butternut Squash Freezing Protocol

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The organic Butternut squash (Cucurbita moschata), harvested at a commercially mature stage in the Polatli district of Ankara, was transported to the food processing facility (Mevsim Gida Co., Salihli, Manisa, Türkiye), where they were subjected to an industrial freezing process using the individual quick freezing (IQF) (Frigoscandia FloFreeze® MX, Helsingborg, Sweden) technique according to the flow chart provided in Figure 1. The cutting procedure employed prior to freezing process refers to obtaining 10 × 10 mm pieces using an industrial food cutter (Urschel DiversaCut Sprint® Dicer, Chesterton, IN, USA). The final product is supplied as raw material to a renowned baby food manufacturer. Within the scope of this study, samples collected on three different production days from six points indicated in the flowchart were transferred to the laboratory with a cold chain to minimize quality loss. The collected samples were ground into a fine powder using a grinder (Büchi Mixer B-400, Flawil, Switzerland) and stored in a −80 °C freezer (Ultra-Low Temperature Freezer MDF-U5386S, Panasonic Co., Osaka, Japan) until analysis.
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10

Blueberry Cultivation and Sample Preparation

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The plant material used was 6-year-old rabbiteye blueberry 'Kunisato 35 gou', cultivated in the research field of the Faculty of Agriculture, University of Miyazaki (31 • 49 ′ 41.2 ′′ N 131 • 24 ′ 41.0 ′′ E), while 8-year-old rabbiteye blueberry 'Homebell' was cultivated as a control. 'Kunisato 35 gou' was planted densely using the method of Toyama et al. [5] (link). 'Homebell' was planted at a 3 m spacing for fruit cultivation and grown according to usual methods. The branches and leaves of each cultivar were collected every 2 months starting in April. In addition, samples of each leaf and branch were collected at different times of the year from three independent plants.
The collected branches and leaves were frozen in situ and dried in a freeze-dryer (FDU-2100, EYELA, Tokyo, Japan) and a dry chamber (DRC-1000, EYELA, Tokyo, Japan). These dried samples were ground using a mixer (BUCHI Mixer B-400, BUCHI, Tokyo, Japan) and maintained in a -20 • C freezer.
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