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Mls 1200

Manufactured by Milestone
Sourced in Italy

The MLS 1200 is a laboratory equipment designed for general scientific applications. It features a compact and durable construction, and is capable of performing various standard laboratory tasks.

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9 protocols using mls 1200

1

Microwave Digestion and ICP Analysis

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The oven dried plant samples were ground and digested in 5:1 (v/v) HNO3:HClO4 (5 mL) in a microwave oven (MLS 1200, Milestone, FKV, Boldone, Italy). The Cd and Mo concentrations were measured in the digested samples by inductively coupled plasma (ICP)-optical emission spectroscopy (Vista-PRO, Varian, Inc., Palo Alto, California, CA, USA) and ICP-mass spectrometry (ICP-MS) (ELAN DRC-e, Perkin-Elmer Sciex, Wilmington, DE, USA) [27 (link),28 (link)].
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2

Elemental Analysis of Owl Pellets

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The owl pellets were measured for length, breadth, and weight and dried in a hot-air oven over 24 h at 105 °C until no weight reduction occurred. Pellet remnants were ground using a homogenizer and were weighed using a weighing balance. Element residues (µg/g) in the pellets were assessed on a dry weight (DW) basis [6 (link)]. Five grams of the pellet was digested using a microwave digester (Milestone, MLS 1200) using 10 mL nitric acid (HNO3; 69% GR) for 10 min, 1 mL perchloric acid (HClO4; 70% GR) for 5 min. and 5 mL hydrogen peroxide (H2O2 30% GR) for 10 min at 250 W magnetron power using the acid digestion method [14 (link)]. The digested solutions were shifted using filter paper and were kept in a deep freezer until analysis. Metals such as chromium (Cr), manganese (Mn), cobalt (Co), molybdenum (Mo), selenium (Se), vanadium (V), copper (Cu), nickel (Ni), lead (Pb), zinc (Zn), and iron (Fe) were determined using ICP-MS (inductively coupled plasma mass spectrometry). After being run in triplicate, the quantification and the average were used for further analysis. The detection limits (μg/kg d.w.) were as follows: Cr 0.1, Mn 0.1, Co 0.1, Mo 0.1, Se 0.1, V 0.1, Cu 0.1, Ni 0.1, Pb 0.1, Zn 0.1, and Fe 0.1. The recoveries were adjusted between 95 and 101 % for all of the metals analysed.
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3

Quantitative Elemental Analysis of Stainless Steel Powders

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The elemental composition of the three stainless steel powders used was measured after 10 mg portions were dissolved in a mixture of 2 mL of aqua regia and 0.5 mL of hydrofluoric acid with microwave-assisted heating (MLS 1200, Teflon container SV140, 10 bar, Milestone, 556 J. Sorisole, Italy). Before digestion, 10 µg of beryllium (as chloride) was added as internal standard before dilution to 15 mL with de-ionized water. The elemental composition was measured with a Perkin-Elmer Optima Model 7300 DV inductively coupled plasma optical emission spectrometer (Perkin-Elmer Inc., Waltham, MA, USA).
After removing the TEM grids from the air filter surface, the same analytical procedure was used for measurement of the elemental content of the particulate matter collected by the filters.
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4

Boron Uptake Kinetics in Cells

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A total of 4×105 cells were seeded in 6 cm culture dishes for 48 hours, and 2 mL medium containing 25 μg 10B/mL BA was added to the cells for 0, 30, 60, 90, and 120 minutes. Then, the cells were collected after washing with 1 mL 4 °C phosphate-buffered saline (PBS) three times. After that, 65% nitric acid (Merck, Darmstadt, Germany) and 30~35% hydrogen peroxide were mixed with the samples in Teflon high-pressure digestion vessels. The samples were dissolved into solution by a microwave digestion system (MLS 1200; Milestone, Italy). The boron concentrations were measured by inductively coupled plasma atomic emission spectroscopy (ICP‒AES; OPTIMA 2000 DV; PerkinElmer Instruments, Norwalk, CT, USA).
A total of 2.4×106 cells were seeded in 10 cm culture dishes and incubated for 48 hours. Six milliliters of medium containing 25 μg 10B/mL BA was added to the cells for 30 minutes. The cells were then washed with 2 mL of 4 °C PBS three times and harvested. Subsequently, the cells were digested and measured for boron concentration following the same process as the boron uptake time course.
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5

Elemental Analysis of Plant Samples

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The plant samples were dried, grinded, weighed, and soaked with sulfuric acid and digested in a fume hood at 180 °C for 3 h, followed by the addition of H2O2. K concentration was then determined with a flame photometer (Model 410, Sherwood, USA).
For the determination of calcium (Ca); magnesium (Mg); and other micronutrients zinc (Zn), iron (Fe), manganese (Mn), and copper (Cu), dried plant samples were digested in 4:1 (v/v) HNO3:HClO4 (v/v) in a microwave oven (MLS 1200, Milestone, FKV, Italy). The elements (Ca, Mg, Zn, Fe, Mn, and Cu) concentrations in the digested samples were determined by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS).
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6

Microwave-Assisted Sediment Digestion

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One gram of powdered sediment sample was transferred to a Teflon digester tube in a microwave digestion system (Milestone, MLS 1200), which was programmed to have the sequential addition of a series of acids, i.e. 10 ml HNO3 for 10 min, 1 ml HClO4 for 5 min, and 5 ml H2O2 for 10 min, at 250W magnetron power settings29 (link). A digestion blank without a sample was also included. By adding deionized water, the digested samples were filtered, made up to 50 ml, and stored in pre-cleaned and acid-treated plastic vials at 4°C53 .
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7

Molybdenum and Cadmium Analysis in Rice

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The aromatic rice plant leaves were sampled at three prominent growth stages and ears (at reproductive stage) and grains (at maturity stage) and oven dried for estimating Mo and Cd concentrations. The plant samples (0.3 g) were digested in 5:1 (v/v) HNO3:HClO4 (5 mL) in a microwave oven (MLS 1200, Milestone, FKV, Italy). Mo and Cd concentrations were measured by ICP-mass spectrometry (ICP-MS) (ELAN DRC-e, PerkinElmer SCIEX, DE) and Atomic Absorption Spectrophotometer (AAS) (AA6300C, Shimadzu, Japan) [2 (link),27 (link)].
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8

Determination of Cd and As in Rice

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Filled rice grains were ground to fine powder after oven drying at 70°C. Samples (0.5 g) were digested in 5 : 1 (v/v) HNO3/H2O2 (5 mL) in a microwave oven for 30 minutes (MLS 1200, Milestone, FKV, Italy) [16 ]. Cd and As concentrations in the digested samples were determined by inductively coupled plasma- (ICP-) optical emission spectroscopy (Vista-PRO, Varian, Inc., Palo Alto, CA,) and ICP-mass spectrometry (ICP-MS) (ELAN DRC-e, Perkin-Elmer Sciex, DE). Accuracy was evaluated by the use of a certified reference material (rice flour, NMIJ CRM 7502-a No.7 Cd Level II).
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9

Quantification of Heavy Metals in Scats

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The scats’ length, breadth, and weight were measured and dried using a hot sterilizer for 24 h at 105 °C. The scat remnants were homogenized and weighed using an electronic balance [16 (link)]. Five grams of the homogenized dry scat was digested using a microwave digester (Milestone, MLS 1200) with 10 ml of nitric acid (69% grade) for 10 min, and 1 ml of perchloric acid (70% grade) for 5 min [17 (link)]. The digested samples were left in a deep freezer until metal analysis, such as Cr, Cu, and Pb, using atomic absorption spectroscopy (AAS) [18 (link),19 (link)].
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