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10 protocols using coomassie reagent

1

Biochemical Reagents and Compounds

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Potassium mono and dibasic phosphates, ammonium sulfate, sodium citrate, magnesium sulfate, glucose and glycerol were from Fisher Scientific. N,N-dimethyl-p-phenylenediamine was from Fluka, and Coomassie reagent was from Thermo Scientific. All other chemicals were from Sigma.
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2

Protein Quantification by Bradford Assay

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Protein concentrations in preparations were determined by the Bradford protein assay69 (link). The reactions were conducted according to the manufacturer’s protocol for the Coomassie reagent (Thermo Scientific, USA). The protein concentration was determined by the calibration curve plotted for an aqueous solution of BSA (Sigma, USA) within the range of 1–25 μg/mL.
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3

Nitration and Quantification of Human ApoAI

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Purified human HDL (MyBioSource, # MBS173147, total protein 40 mg/ml, standard curve range 1–12 ng/ml) was used as standard for the determination of plasma concentrations of apoAI. For NT-apoAI standard, purified human apoAI (Biomedical Technologies, # BT-927) was nitrated with sodium nitrite 23 (link), 24 (link). Briefly, purified apoAI (~ 1 mg/ml) was adjusted to pH 3.5 and mixed with 200 mM sodium nitrite and then incubated at 37°C for 24 h under low agitation. Samples were dialyzed against phosphate buffer saline (PBS) for 24 h at 4°C, and protein concentration was determined by the Coomassie Reagent (Thermo Scientific, #23236) and bovine serum albumin (BSA) as a standard 25 (link). The amounts of nitrated tyrosines in the modified apoAI were determined using a commercially available NTyr ELISA kit based on nitrated albumin (Cell Biolabs, # STA-305) as described by the manufacturer. The nitrated apoAI (0.7 mg/ml protein) contained 2000 nM NT-apoAI giving a concentration of 80 mmol of nitrated tyrosine per mol of apoAI.
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4

Cervicovaginal Fluid HBD2 Quantification

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Filter-sterilised BSA (Sigma-Aldrich) served as a standard. Coomassie reagent (Thermoscientific, Paisley, UK) was used according to manufacturer’s instructions. Cervicovaginal fluid HBD2 levels were determined by ELISA (Peprotech ELISA Development Kit, according to manufacturer’s instructions). HBD2 protein was undetectable in 25 samples; the lower limit of detection (16pg/ml) divided by the square root of 2 was substituted [13 ].
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5

Quantification of Cervicovaginal HBD2

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Filter-sterilised bovine serum albumin (Sigma-Aldrich) served as a standard. Coomassie reagent (Thermoscientific, Paisley, UK) was used according to the manufacturer’s instructions. Cervicovaginal fluid HBD2 levels were determined by ELISA (Peprotech ELISA Development Kit, according to the manufacturer’s instructions). HBD2 protein was undetectable in 25 samples; the lower limit of detection (16 pg/ml) divided by the square root of 2 was substituted [13 ].
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6

Extracellular Protein Quantification

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Fungal growth supernatant was collected by centrifugation (4770 g × 20 min, 4 °C), and the concentration of extracellular protein was measured using the Coomassie (Bradford) Protein Assay Kit (Thermo Fisher Scientific Inc., Waltham, MA, USA). According to the protocol provided, 100 μl fungal growth supernatant was mixed well with 100 μl Coomassie reagent in a 96-well plate (Thermo Fisher Scientific Inc., USA) and left for 15 min. The absorbance was measured at 595 nm using a μQuant microplate spectrophotometer (BioTek Instruments, Inc., Winooski, VT, USA). Protein concentrations were estimated by reference to the absorbance obtained for a dilution series of bovine serum albumin (BSA) standards (Thermo Fisher Scientific Inc., USA).
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7

Bradford Protein Quantification Protocol

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The total protein concentration in the samples was measured by the Bradford method [59 (link)]. The reaction was carried out according to the protocol for the proprietary Coomassie reagent (Thermo Fisher Scientific, Waltham, MA, USA). The protein concentration was determined by a calibration curve constructed for an aqueous solution of BSA (Sigma, Ronkonkoma, NY, USA) within the range of 1 to 25 µg/mL.
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8

Optimized Enzyme Activity Assays

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Medium and buffer components were purchased from Fisher Chemical. Amino acids, casAmino acids (acid-hydrolyzed), copper sulfate, ferrous ammonium sulfate, cytochrome c, horseradish peroxidase (HRP), Amplex Red, hydrogen peroxide solution (30% w/w), bovine catalase, ascorbic acid, ovalbumin, β-mercaptoethanol, N-acetylcysteine, bovine superoxide dismutase, reduced (GSH) and oxidized (GSSG) glutathione, E. coli alkaline phosphatase (catalog P5931), ascorbate, p-nitrophenylphosphate, zinc(II) diacetate, guanidinium HCl, citraconate, diethylenetriaminepentaacetic acid (DTPA), EDTA, NADH, NAD+, recombinant E. coli formate dehydrogenase (FDH), rabbit L-lactate dehydrogenase, xanthine, bovine xanthine oxidase, and antibiotics were from Sigma Aldrich. Coomassie reagent was from Thermo Scientific. Formyl-Met-Ala-Ser was from Bachem.
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9

Radiolabeled Amino Acid Transport Assay

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l-Cysteine hydrochloride monohydrate, l-cystine dihydrochloride, and other nonradioactive amino acids were purchased from Sigma-Aldrich. A 30% (wt/wt) solution of hydrogen peroxide (H2O2), bovine catalase, ovalbumin, O-nitrophenol-β-galactoside (ONPG), diethylenetriamine pentaacetic acid (DTPA), dithiothreitol (DTT), 2,2′-dipyridyl, β-mercaptoethanol, antibiotics, and 5-bromo-4-chloro-3-indolyl-β-d-galactopyranoside (X-Gal) were purchased from Sigma-Aldrich. Coomassie reagent was from Thermo Scientific. Medium reagents and buffer chemicals were from Fisher Chemical. Restriction and ligation enzymes were from New England BioLabs. Qiagen kits were used for genomic and plasmid DNA preparation. Colony PCR beads were from GE Healthcare, and PCR reagents were purchased from Invitrogen. DNA sequencing was performed at ACGT, Inc. Radiolabeled l-[1,2,1′,2′-14C]cystine and l-[14C(U)]leucine were purchased from Perkin Elmer; we note that putative radiolabeled cystine that was received from another supplier was found not to be authentic cystine. Transport measurement filters were purchased from Millipore Sigma (GSWP02500).
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10

Ureter Tissue α-SMA and TGF-β Analysis

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Tissue analyzes of α-SMA and TGF-β were performed in the ureter tissue homogenates (Witeg Labortechnik GmgH, WiseTis HG-15D Homogenizer). After two freeze-thaw cycles, the homogenates were centrifuged for 5 minutes at 5000 g (2-8 °C). In the supernates, α-SMA and TGF-β levels were assayed using appropriate enzyme-linked immunosorbent assay (ELISA) kits (Cusabio CSB-E14027r and Boster EK0514, respectively). The analyses were performed according to the product instruction and read using an absorbance microplate reader (BioTek, ELx800). The concentration of total proteins in the homogenates was determined by the Bradford method using Coomassie reagent (Thermo scientific; 23200) and bovine serum albumin as standard.
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