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5 protocols using glass microfiber filter

1

Electrochemical Performance of NaAlTi3O8 Composite Electrodes

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For electrochemical testing, composite electrodes were prepared. Carbon black (99+ % purity, Alfa Aesar) was ball-milled with the active material with a weight ratio of 15:85 at 600 rpm for 1 hour. Then the mixture, additional Carbon black, and Polyvinylidene fluoride (PVDF) (Sigma-Aldrich) were blended with a weight ratio of 8:1:1, using N-Methyl-2-pyrrolidone (NMP) (J.T.Baker) as solvent. The slurry was then applied on aluminum foil and dried in an oven at 60 °C for 2 h. The dried film was pressed with using a roller-press (MTI Corp.) to densify the electrode. The film was then cut into circular discs of 15 mm diameter using a disc cutter (MTI Corp. MSK-T-07). Standard CR2016 coin cell was assembled by using sodium foil (99.95% purity metal basis, Sigma-Aldrich) as anode, NaAlTi3O8 composite electrode as cathode, 1 M NaPF6 (Sigma-Aldrich) in ethylene carbonate/diethylene carbonate (EC : DEC) as electrolyte, and Glass Microfiber Filter (VWR) as separator, in an argon filled glove box (MBraun). The cycling of coin cell was conducted with using a battery cycler (Arbin, BT2043), with voltage windows of 0.01 - 2.5 V or 0.1 - 2.5 V under rates of C/10, C/5, and 1 C. All electrochemical tests were performed under ambient temperature.
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2

Comprehensive Protein Quantification Protocol

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Bromocresol green, citric acid, Coomassie brilliant blue (CBB) (G-250), copper sulfate, Folin-Ciocalteau (FC) reagent, O-phosphoric acid, sodium carbonate, sodium hydroxide, sodium potassium tartrate, succinic acid, and tri-sodium citrate were purchased from Thermo Fisher Scientific India Pvt. Ltd., India. Bicinchoninic acid and tetrabromophenol blue were purchased from Carbosynth Limited, Compton, Berkshire, UK. Sodium bicarbonate was purchased from NICE Chemicals Pvt. Ltd., India. Ethanol (>99%) was purchased from Changshu Jangyuan Chemical, China. Bovine serum albumin (BSA) – Fraction V, purchased from Himedia Laboratories Pvt. Ltd., India, was used as standard protein throughout the research. Reagent grade triple deionized distilled water was purchased from Marech Pvt. Ltd., Lalitpur, Nepal. Whatman No. 1 filter paper was purchased from Whatman International Ltd, Maidstone, England, and glass microfiber filter was purchased from VWR International, Pennsylvania, USA. Epoch™ microplate spectrophotometer (Biotek instruments, Inc., USA) was used for spectrophotometric determination of proteins in serum and urine samples.
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3

Quantifying Biomass of Spirulina platensis

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Culture samples of L. platensis PCC7345 were analysed using a UV/VIS spectrophotometer (GENESYS 150, Thermo Fisher, Waltham, MA, USA). The optical density (OD750) was measured at 750 [nm] and was calibrated against Cx [g L−1] of L. platensis PCC7345 using the following correlation (in triplicate, [26 (link)]): Cx=0.86 × OD750
Aiming to assess Cx, 15 mL of L. platensis PCC7345 suspension was passed through a glass microfiber filter (VWR International, Delaware Valley, PA, USA, mesh size: 1 [µm], in triplicate) and was then washed three times using 15 mL deionised water and dried for 24 h at 103 °C (Memmert GmbH + Co.KG, Schwabach, Germany). Finally, the weight difference of dried biomass was determined to calculate Cx [26 (link)].
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4

Methionine Incorporation in Yeast

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Yeast cells were grown to an A600 of 0.6 in SD selective medium supplemented with 2% raffinose. Cells were then resuspended at an A600 of 0.3 in 2% galactose containing SD selective medium for 4-10 hours in order to induce either PAP, AtBI-1 or mutant forms of AtBI-1. At time zero, 35 (link) methionine was added to cells growing on galactose. At the various times post-induction, 600 ml of yeast cells were taken for growth measurements and an aliquot of 800 ml were assayed for methionine incorporation in triplicate as described by Parikh et al. 2002. Briefly, the yeast were added to 200 ml of 100% trichloroacetic acid and incubated for 10 min on ice followed by 20 min at 70°C. The precipitate then filtered through 24-mm glass microfiber filters (VWR), washed with ice-cold 5% trichloroacetic acid followed by 95% ethanol. Filters were dried overnight and incorporation was quantified in a scintillation counter. The Cpm was normalized to the A600 reading.
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5

Wastewater Treatment Characterization Protocol

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The following analyses were performed to characterize the influent, effluent and sludge characteristics: COD, DOC, pH, Cl -, conductivity, PO 4 If necessary for the analyses, samples were filtered before they were analysed using glass microfiber filters of 1.2µm from VWR (Belgium, Leuven). MLSS, MLVSS and SVI were measured in accordance with the procedures described in Standard Methods for the Examination of Water and Wastewater [37] .
Settling characteristics were determined with a 1L graduated cylinder with a height of 34.5 cm and an internal diameter of 6.1 cm. Activated sludge morphology was observed with a Motic BA 310 microscope by using an EF-N Plan 10x0.25 ocular.
Measurements were always done at the end of the aeration phase, so sludge was always in an endogenous state.
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