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Rs 60

Manufactured by Biosan
Sourced in Poland, Latvia

The RS-60 is a laboratory centrifuge designed for general-purpose applications. It features a maximum speed of 6,000 rpm and a maximum RCF of 3,220 x g. The centrifuge can accommodate sample volumes up to 150 mL.

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4 protocols using rs 60

1

Functional Beverage Formulation with Sprouts

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The composition was designed based on the previously developed recipes for functional beverages. The output drinks contained 30% carrot, 30% pumpkin, and 40% lentil sprouts (C), 30% carrot, 30% pumpkin, 30% lentil sprouts, and 10% broccoli sprouts and parsley leaves (C1), and 30% carrot, 30% pumpkin, 30% lentil sprouts and 10% raspberry, strawberry (C2) [6 (link),7 (link)]. The detailed composition of the studied beverages is presented in Table 1.
In the current study, the sprout lentil flour was replaced by the AGF. Additionally, functional flaxseeds gum (FSG) was added to the recipes (from 0 up to 15% (w/w)). Powdered beverages (0.5 g) were rehydrated in 10 mL Milli-Q water, shaken (3 intervals, 30 s) at room temperature using a multi-rotator (RS-60, Biosan, Otwock, Poland) (300 rpm), and used for analysis.
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2

Determination of Free Reducing Sugars in Beverages

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For the free reducing sugar determination, the beverages were mixed with 50% methanol and extracted for 30 min. with 300 rpm (RS-60, Biosan). The samples were centrifuged at 12,000× g at 4 °C for 20 min, and the free reducing sugar content was determined by using the DNSA method [32 (link)]. Free reducing sugars were expressed in mg per 100 mL of beverages.
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3

Protein Quantification in Beverages

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The beverage was mixed with 1 mol L−1 NaOH and extracted for 30 min. with 300 rpm (RS-60, Biosan). The samples were centrifuged (15 min, 6000× g) and protein content was determined using the Bradford method [30 (link)]. Total protein was expressed as albumin equivalents in mg per 100 mL of beverages.
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4

Biochemical Analysis of Drought-Stressed Plants

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Plant leaves for analysis of biochemical parameters were collected 20 days after induced drought stress from all plants included in each treatment. The lyophilized plant tissue was milled to a particle size of 0.2 mm on a centrifugal mill (Retsch ZM-200, Haan, Germany). Samples (50 mg) were homogenized with 2.4 mm glass beads (Omni kit 19-670, Kennesaw, GA, USA) for 1 min at 5 ms−1 in 1.5 mL of aqueous methanol (80:20, methanol: water, v/v) using a bead mill (Omni Bead Ruptor Elite, Kennesaw, GA, USA). The samples were left to macerate for 1 h on a rotator (Biosan RS-60, Riga, Latvia) and subsequently centrifuged for 5 min at 16,000× g. The supernatants were filtered through a 0.22 µm nylon filter prior to analysis.
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