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Готові списки джерел за темами / Coomassie Brilliant Blue (CBB) / Статті в журналах

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Статті в журналах з теми "Coomassie Brilliant Blue (CBB)"

Автор: Grafiati

Опубліковано: 7 червня 2025

Оновлено: 2 серпня 2025

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1

Rai, Anshuman, Vandana Sirotiya, Ankesh Ahirwar, et al. "Textile dye removal using diatomite nanocomposites: a metagenomic study in photosynthetic microalgae-assisted microbial fuel cells." RSC Advances 15, no. 11 (2025): 8300–8314. https://doi.org/10.1039/d5ra00793c.

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2

Maity, Mritunjoy, Sandip Dolui, and Nakul C. Maiti. "Hydrogen bonding plays a significant role in the binding of coomassie brilliant blue-R to hemoglobin: FT-IR, fluorescence and molecular dynamics studies." Physical Chemistry Chemical Physics 17, no. 46 (2015): 31216–27. http://dx.doi.org/10.1039/c5cp04661k.

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3

Goren, M. P., and J. T. Li. "The Coomassie Brilliant Blue method underestimates drug-induced tubular proteinuria." Clinical Chemistry 32, no. 2 (1986): 386–88. http://dx.doi.org/10.1093/clinchem/32.2.386.

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Abstract The sensitivity of the Coomassie Brilliant Blue (CBB) procedure differs for different proteins. To investigate the impact of this variability on clinical measurements of proteinuria, we collected urine specimens from patients with glomerular disease or drug-induced tubular nephrotoxicity and compared urinary protein concentrations as determined by the CBB method with those obtained by the biuret method. The CBB method underestimated the protein concentration predicted by the biuret method by as much as eightfold in specimens with low proportions of albumin. Determinations of protein b

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4

Ata, Sadia, Muhammad Imran Din, Atta Rasool, Imran Qasim, and Ijaz Ul Mohsin. "Equilibrium, Thermodynamics, and Kinetic Sorption Studies for the Removal of Coomassie Brilliant Blue on Wheat Bran as a Low-Cost Adsorbent." Journal of Analytical Methods in Chemistry 2012 (2012): 1–8. http://dx.doi.org/10.1155/2012/405980.

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The sorption studies of coomassie brilliant blue (CBB) from aqueous solution have been carried out on wheat bran (WB). Coomassie brilliant blue on wheat bran was used to study the adsorption behavior under various parameters such as pH, dosage amount, and contact time. It was observed that under optimized conditions up to 95.70% dye could be removed from solution onto WB. Langmuir and Freundlich adsorption isotherms were used to elaborate the results. Freundlich model was found to be fitted well and favored multilayer adsorption. The Freundlich constants n and KF were determined as 0.53 and2.5

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5

ANJUM, HUSSAIN, and V. CHITRE A. "Electrochemical Potentials in Bovine Serum Albumin (BSA) and Coomassie Brilliant Blue (CBB) Interaction." Journal of Indian Chemical Society Vol. 74, Jan 1997 (1997): 50–51. https://doi.org/10.5281/zenodo.5877555.

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<strong>Chemistry Department, Sophia College for Women, Bhulabhai Desai Road. Bombay-400 </strong><em>026</em> <em>Manuscript received 10 March 1995, revised 30 June 1995, accepted 6 July 1995</em> Electrochemical Potentials in Bovine Serum Albumin (BSA) and Coomassie Brilliant Blue (CBB) Interaction

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6

Verma, Shiv Kumar, Anand Kumar, Moti Lal, and Mira Debnath. "Biodegradation of Synthetic Dye by Endophytic Fungal Isolate in Calotropis procera Root." International Journal of Applied Sciences and Biotechnology 3, no. 3 (2015): 373–80. http://dx.doi.org/10.3126/ijasbt.v3i3.13136.

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In this study, based on colony morphology characteristics, a total of 19 fungal endophytes were isolated from root of Calotropis Procera a traditional Indian medicinal plant. All fungal isolates were screened for their dye degradation ability. The dyes used as test dyes were Rose Bengal (RB), azo dye Methyl Red (MR), Coomassie Brilliant Blue (CBB) and Methylene Blue (MB) and the concentration of each dye in the experiment was kept 100mg/L. Among the 19 fungal endophytic isolates (CPR1-CPR19), only one isolate CPR4 showed strong dye decolourization capability against all the four test dye. Dye

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7

Ameen, Maad M. "Influence of Coomassie Brilliant Blue dye Doping on the Physical Properties of Hydrothermally Synthesized Cu-Sb-S Nanocomposites." Scientia. Technology, Science and Society 2, no. 5 (2025): 39–55. https://doi.org/10.59324/stss.2025.2(5).04.

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This research examines the effects of Coomassie Brilliant Blue (CBB) incorporation on Cu-Sb-S nanocomposite thin films synthesized through hydrothermal methods. Samples were prepared with varying CBB concentrations (0, 0.01, 0.03, and 0.05 gm) and comprehensively known to have structural, morphological, optical, and electronic characteristics. XRD analysis successfully verified forming crystalline phases, with patterns showing characteristic peaks that evolved with increasing CBB content. Based on the X-ray diffraction results. The crystal formations of the products, Cu3SbS3, Cu3SbS4, and Na2C

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8

Ameen, Maad M. "Influence of Coomassie Brilliant Blue dye Doping on the Physical Properties of Hydrothermally Synthesized Cu-Sb-S Nanocomposites." Scientia. Technology, Science and Society 2, no. 5 (2025): 39–55. https://doi.org/10.59324/stss.2025.2(5).04.

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This research examines the effects of Coomassie Brilliant Blue (CBB) incorporation on Cu-Sb-S nanocomposite thin films synthesized through hydrothermal methods. Samples were prepared with varying CBB concentrations (0, 0.01, 0.03, and 0.05 gm) and comprehensively known to have structural, morphological, optical, and electronic characteristics. XRD analysis successfully verified forming crystalline phases, with patterns showing characteristic peaks that evolved with increasing CBB content. Based on the X-ray diffraction results. The crystal formations of the products, Cu3SbS3, Cu3SbS4, and Na2C

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9

Sharma, Pratibha, and Jayshree Rathore. "Sunlight Induced Photogalvanics for Conversion and Storage of Solar Energy: Coomassie Brilliant Blue-Isopropyl Alcohol-Sodium Lauryl Sulphate System." Oriental Journal Of Chemistry 39, no. 4 (2023): 1059–63. http://dx.doi.org/10.13005/ojc/390432.

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Research plan was proposed for systematic observation with scientific way in the solar cell field of photogalvanics. It was analysis of experimental work under the solar energy output. The study of photogalvanic was done for solar energy conversion and storage by using of dye as Coomassie Brilliant Blue CBB), reductant as Isopropyl alcohol (IA), and surfactant as Sodium Lauryl Sulphate (SLS). For this purpose, a specially designed H shaped photogalvanic system was used under investigation for innovative results. Different scientific instruments were used for methodology set up i.e., pH meter (

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10

Zhang, Mengyue, Fan Yang, Nan Wang, et al. "Ultra-Fast Removal of CBB from Wastewater by Imidazolium Ionic Liquids-Modified Nano-Silica." Molecules 30, no. 1 (2024): 24. https://doi.org/10.3390/molecules30010024.

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The efficient removal of dyes is of significant importance for environmental purification and human health. In this study, a novel material (Si-MPTS-IL) has been synthesized by the immobilization of imidazole ionic liquids (ILs) onto nano-silica using the radiation grafting technique. The adsorption performance of Si-MPTS-IL for Coomassie Brilliant Blue (CBB) removal is studied by a series of static adsorption experiments. It is found that Si-MPTS-IL has ultra-fast adsorption kinetics, reaching equilibrium within 2 min. The adsorption process for CBB conforms to the Langmuir model. In addition

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11

Shiba, K. S., K. Kanamori, T. Harada, et al. "A cause of discrepancy between values for urinary protein as assayed by the Coomassie Brilliant Blue G-250 method and the sulfosalicylic acid method." Clinical Chemistry 31, no. 7 (1985): 1215–18. http://dx.doi.org/10.1093/clinchem/31.7.1215.

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Abstract In simultaneous assays of urinary proteins by the Coomassie Brilliant Blue G-250 (CBB) and the sulfosalicylic acid (SSA) methods, we noticed that about 18% of samples showed about twice higher protein values by the former method than by the latter. Some urinary proteins are soluble in SSA and react with CBB. Examinations with sodium dodecyl sulfate/polyacrylamide gel electrophoresis showed that these proteins migrated in 13 protein bands having relative molecular masses ranging from 15 000 to 230 000. The protein corresponding to the most intensely stained band in urine samples from t

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12

Zhao, Yi, Xiao Ying Lv, Zheng Lin Jiang, Xia Li, Yan Huang, and Zhi Gong Wang. "Silicon Nitride Surface Modification and Cell Adhesion." Materials Science Forum 610-613 (January 2009): 1022–25. http://dx.doi.org/10.4028/www.scientific.net/msf.610-613.1022.

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Silicon microelectrode arrays (Si MEAs) have great potential in recording of neural activity; the biocompatibility of silicon nitride has gained much attention as a part of Si MEAs. In this study, we used alternating polycations, polyethyleneimine (PEI), and polyanions, gelatin, to fabricate multilayer films built up by LbL deposition on silicon nitride wafers. Then the samples surfaces were characterized by contact angle system and atomic force microscopy (AFM). The amount of proteins adsorbed on silicon nitride and modified silicon nitride were measured by a modified Coomassie brilliant blue

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13

Chen, Ruijuan, Zahra Jalili, and Reza Tayebee. "UV-visible light-induced photochemical synthesis of benzimidazoles by coomassie brilliant blue coated on W–ZnO@NH2 nanoparticles." RSC Advances 11, no. 27 (2021): 16359–75. http://dx.doi.org/10.1039/d0ra10843j.

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A new photochemical route is disclosed in the preparation of a wide range of benzimidazoles in air under the illumination of an HP mercury lamp in the absence of any oxidizing species catalyzed by heterogenized W–ZnO@NH<sub>2</sub>–CBB.

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14

Shad, Naveed A., Mehvish Zahoor, Khizra Bano, et al. "Synthesis of flake-like bismuth tungstate (Bi2WO6) for photocatalytic degradation of coomassie brilliant blue (CBB)." Inorganic Chemistry Communications 86 (December 2017): 213–17. http://dx.doi.org/10.1016/j.inoche.2017.10.022.

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15

Gerbaut, L., and M. Macart. "Is standardization more important than methodology for assay of total protein in cerebrospinal fluid?" Clinical Chemistry 32, no. 2 (1986): 353–55. http://dx.doi.org/10.1093/clinchem/32.2.353.

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Abstract Four manual micromethods for protein determination, two turbidimetric (trichloroacetic and sulfosalicylic acid-sodium sulfate) and two colorimetric (Lowry and Coomassie Brilliant Blue--sodium dodecyl sulfate, CBB-SDS) were used to compare the standard curves for total protein (0.30 to 3 g/L) produced with three reference materials: bovine serum albumin, human serum albumin, and diluted human serum. We measured the apparent protein content of a sample of pooled human cerebrospinal fluid by all four methods and with use of all three standards. The only reference material that gave simil

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16

Paddock, S. W. "Tandem scanning reflected-light microscopy of cell-substratum adhesions and stress fibres in Swiss 3T3 cells." Journal of Cell Science 93, no. 1 (1989): 143–46. http://dx.doi.org/10.1242/jcs.93.1.143.

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This paper describes two applications of the tandem scanning reflected-light microscope (TSM) for the observation of the structure of individual cells growing in tissue culture. First, the TSM is used as an alternative to interference reflection microscopy (IRM) or total internal reflection aqueous fluorescence microscopy (TIRAF) to observe cell-substratum adhesions in unstained living cells growing on a glass coverslip. Second, the TSM is used to produce improved images of cellular structures in 3T3 cells stained with various protein dyes including Napthol Blue Black (NBB) and Coomassie Brill

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17

Yan, Huang, Xiao Ying Lü, and Nan Huang. "Study of Protein Adsorption and Conformational Change on DLC and Ti Surfaces Using FTIR and Coomassie Brilliant Blue Protein Assay." Key Engineering Materials 330-332 (February 2007): 893–96. http://dx.doi.org/10.4028/www.scientific.net/kem.330-332.893.

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The aim of present work was to study the interaction between human plasma protein-albumin (Alb) and immunoglobulin G (IgG) and the surfaces of two kinds of diamond-like carbon (DLC-A and DLC-B) and titanium (Ti) film. Fourier transform infrared spectroscopy (FTIR) was used to perform both quantity investigation and secondary structure analysis of above two proteins adsorbed on material surfaces. A modified Coomassie brilliant blue (CBB) protein assay was also used to study the amount of adsorbed proteins. The result of FTIR quantitative evaluation shows that the ratio of adsorbed Alb to IgG (R

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18

Biuki, Mozhgan, Hassan Zavvar Mousavi, Majid Arvand, and Hadi Fallah Moafi. "Application of magnetite nanoparticle-modified walnut shell as an adsorbent for the removal of the organic dye Coomassie Brilliant Blue R-250." Journal of the Serbian Chemical Society, no. 00 (2024): 95. http://dx.doi.org/10.2298/jsc240421095b.

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In this research, a magnetic nanocomposite, walnut shell@Fe3O4, was synthesized as a natural adsorbent for the removal of Coomassie Brilliant Blue (CBB) R-250 organic dye from aqueous solutions, achieving a remarkable removal efficiency of 96.16%. The morphology of the nanocomposite was characterized using SEM and FTIR, revealing particle sizes of less than 18 nanometers. Additionally, BET analysis was performed, indicating a high surface area that enhances adsorption capacity. The influential variables affecting dye removal, including solution pH, stirring time, adsorbent dosage, initial dye

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19

Zou, Minmin, Hexin Zhu, Ming Dong, and Tian Zhao. "Template Method for Synthesizing Hierarchically Porous MIL-101(Cr) for Efficient Removal of Large Molecular Dye." Materials 15, no. 16 (2022): 5763. http://dx.doi.org/10.3390/ma15165763.

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As one of the most important prototypical chromium-based MOFs, MIL-101(Cr) is well-studied and widely employed in various scientific fields. However, due to its small capture window sizes and curved internal apertures, its application in large molecular removal is quite limited, and given its high stability and high synthetic temperature (>200 °C), it is difficult to achieve hierarchically porous MIL-101(Cr). In our study, hierarchically porous MIL-101(Cr) involving a high macro-/meso-/micropores ratio was designed and synthesized using acetic acid as an additive and silicon dioxide (SiO2)

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20

Marshall, Thomas, and Katherine M. Williams. "Total Protein Determination in Urine: Elimination of a Differential Response between the Coomassie Blue and Pyrogallol Red Protein Dye-binding Assays." Clinical Chemistry 46, no. 3 (2000): 392–98. http://dx.doi.org/10.1093/clinchem/46.3.392.

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Abstract Background: The total protein content of urine is a good index of renal function, but its determination is unreliable. Protein dye-binding assays are simple, but they characteristically lack a uniform response to different proteins. Methods: We investigated a differential response of the Sigma Microprotein Coomassie Brilliant Blue (CBB) and Pyrogallol Red-molybdate (PRM) protein dye-binding assays to urine, using human albumin, albumin/globulin, or urinary protein as calibrator. Results: The urine protein values (n = 60) obtained with the CBB assay were 110–13 500 mg/L (mean, 2390 mg/

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21

Hajiyeva, Flora. "COOMASSIE BRILLIANT BLUE DYE REMOVAL IN AQUEOUS SOLUTION BY HYDROGEN PEROXIDE IN THE PRESENCE OF IRON OXIDE NANOPARTICLES." New Materials, Compounds and Applications 8, no. 2 (2024): 190–98. http://dx.doi.org/10.62476/nmca82190.

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In this work, was investigated of catalytic oxidative degradation of the Coomassie Brilliant Blue synthetic dye (CBB R-250) by hydrogen peroxide H2O2 in the presence of Fe3O4 magnetite nanoparticles. It was found that in the presence of Fe3O4 magnetic nanoparticles, the dye degradation rate significantly increases, which is explained by the strong interaction of Fe3O4 nanoparticles with hydrogen peroxide with the formation of highly reactive hydroxyl radicals followed by an increase in the rate of oxidative degradation. Also in the article, it was found that the degradation of the СBB R-250 dy

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22

Baradaran, Soroush, and Mohammad Taghi Sadeghi. "Coomassie Brilliant Blue (CBB) degradation using hydrodynamic cavitation, hydrogen peroxide and activated persulfate (HC-H2O2-KPS) combined process." Chemical Engineering and Processing - Process Intensification 145 (November 2019): 107674. http://dx.doi.org/10.1016/j.cep.2019.107674.

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23

Fettman, Martin J. "Comparison of urinary protein concentration and protein/creatinine ratio vs routine microscopy in urinalysis of dogs: 500 cases (1987-1988)." Journal of the American Veterinary Medical Association 195, no. 7 (1989): 972–76. https://doi.org/10.2460/javma.1989.195.07.972.

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Summary The clinical problems and results of urinalyses of 500 dogs were reviewed and summarized to compare the sensitivities for detection of abnormalities indicative oj urinary system disease among qualitative (sulfosalicylic acid [ssa]), quantitative (Coomassie brilliant blue [cbb]), and indexed (urinary protein/creatinine ratio [u(p/c) determinations of urinary protein loss vs microscopic examination of urine sediment. False-negative rates for the detection of microscopically abnormal urine specimens were 5.4% for ssa ≥ 1 +, 8.5% for cbb ≥ 1.0 mg/ml, 9.7% for u(p/c) ≥ 1.0, and 7.7% for cbb

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24

Ezzat, Abdelrahman O., Ahmed M. Tawfeek, Jothi Ramalingam Rajabathar, and Hamad A. Al-Lohedan. "Synthesis of New Hybrid Structured Magnetite Crosslinked Poly Ionic Liquid for Efficient Removal of Coomassie Brilliant Blue R-250 Dye in Aqueous Medium." Molecules 27, no. 2 (2022): 441. http://dx.doi.org/10.3390/molecules27020441.

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In this work, new crosslinked pyridinium poly ionic liquid and its magnetite hybrid structured composite were prepared and applied to remove the toxic dye Coomassie Brilliant Blue (CBB-R250) from aqueous solutions. In this respect, vinyl pyridine, maleic anhydride, and dibromo nonane were used to prepare crosslinked quaternized vinyl pyridinium/maleic anhydride ionic liquid (CQVP-MA). Furthermore, a linear copolymer was prepared by the reaction of vinyl pyridine with bromo nonane followed by its copolymerization with maleic anhydride in order to use it as a capping agent for magnetite nanopart

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25

Chander, Prakash and Shafila Bansal. "Room Temperature Ionic Liquid Based Extraction And Recovery Of Dyes From Their Aqueous Solutions." British Journal of BioMedical Research 03, no. 04 (2019): 1005–20. https://doi.org/10.24942/bjbmr.2019.540.

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An attempt has been made for the removal of cationic/anionic dyes from water using room temperature ionic liquids (RTILs). RTILs <em>viz.</em> 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF<sub>6</sub>]), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIM][NTf<sub>2</sub>]), 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF<sub>4</sub>]) and 2-Hydroxyethyl-trimethylammonium L-(+)-lactate ([(C<sub>2</sub>H<sub>4</sub>OH)-(CH<sub>3</sub>)<sub>3</sub>N][Lactate])/CL have been applied for the removal of dyes like Rhodamine 6G (Rh6G), congo red (CR) and coomassi

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26

Margaretta, Dewi Liliany, Angliana Chouw, Yanni Dirgantara, Melanie Sadono Djamil, and Ferry Sandra. "Macerated-Pineapple Core Crude Extract-derived Bromelain Has Low Cytotoxic Effect in NIH-3T3 Fibroblast." Indonesian Biomedical Journal 7, no. 2 (2015): 101. http://dx.doi.org/10.18585/inabj.v7i2.75.

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BACKGROUND: Bromelain is a sulfhydryl proteolytic enzyme that can hydrolyze protein, protease or peptide. Bromelain can be found in pineapple stem, fruit and core. Bromelain is composed of 212 amino acid residues with cysteine-25 forming a polypeptide chain that can hydrolyze peptide bonds by H2O. In medicine, bromelain has been developed as antibiotic, cancer drug, anti-inflammatory agent and immunomodulator. In dentistry, bromelain has potential to reduce plaque formation on the teeth and to irrigate root canal.METHODS: Pineapple core was dried for 3 days to get simplicia. Then simplicia was

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27

Rozman, Martin, Zala Štukovnik, Ajda Sušnik, et al. "A HepG2 Cell-Based Biosensor That Uses Stainless Steel Electrodes for Hepatotoxin Detection." Biosensors 12, no. 3 (2022): 160. http://dx.doi.org/10.3390/bios12030160.

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Humans are frequently exposed to environmental hepatotoxins, which can lead to liver failure. Biosensors may be the best candidate for the detection of hepatotoxins because of their high sensitivity and specificity, convenience, time-saving, low cost, and extremely low detection limit. To investigate suitability of HepG2 cells for biosensor use, different methods of adhesion on stainless steel surfaces were investigated, with three groups of experiments performed in vitro. Cytotoxicity assays, which include the resazurin assay, the neutral red assay (NR), and the Coomassie Brilliant Blue (CBB)

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28

Radko, Lidia, Wojciech Cybulski, and Wojciech Rzeski. "The Protective Effect of Silybin against Lasalocid Cytotoxic Exposure on Chicken and Rat Cell Lines." BioMed Research International 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/783519.

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Lasalocid, an ionophore coccidiostat, extensive use implies a risk of toxicological impacts. Protective effects of silybin, a herbal compound ofSilybum marianum, are reported elsewhere. The aim of this study was to compare effects of the combined use of lasalocid and silybin in chicken hepatoma cells (LMH) and rat myoblasts (L6) cell lines cultures. The cytoprotective effect resulting from an interaction of both pharmaceuticals was measured with the help of MTT reduction and, coomassie brilliant blue binding (CBB) and LDH release assays. Isobolography and the combination index (CI) estimated t

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29

Algarni, Tahani Saad, Amal M. Al-Mohaimeed, Naaser A. Y. Abduh, Reem Abdulrahman Habab, and Saad Mohammed Alqahtani. "Green Synthesis of Mixed ZnO-SnO2 Nanoparticles for Solar-Assisted Degradation of Synthetic Dyes." Catalysts 13, no. 12 (2023): 1509. http://dx.doi.org/10.3390/catal13121509.

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In this work, ZnO, SnO2, and their mixed ZnO-SnO2(25%) nanoparticles (NPs) were successfully green synthesized in a straightforward manner with a low-cost and environmentally friendly approach using a banana peel extract. The synthesized nanophotocatalysts were characterized using various techniques including FTIR, XRD, UV-Vis, TEM, SEM, BET, PL, EDS, and TGA. The characterization results showed that the ZnO and SnO2 powders were crystallized in a hexagonal wurtzite and rutile-type tetragonal structures, respectively, and their mixed ZnO-SnO2(25%) NPs contain both structures. Also, it was foun

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30

Iskandar, Hikmayani, Göran Andersson, Herry Sonjaya, et al. "Protein Identification of Seminal Plasma in Bali Bull (Bos javanicus)." Animals 13, no. 3 (2023): 514. http://dx.doi.org/10.3390/ani13030514.

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The purpose of this study was to identify seminal plasma proteins in Bali bull and their potential as biomarkers of fertility. Semen was collected from 10 bulls aged 5–10 years using an artificial vagina. Fresh semen was then centrifuged (3000× g for 30 min). The supernatant was put into straws and stored in liquid nitrogen. The semen plasma protein concentration was determined using the Bradford method, and the protein was characterized using 1D-SDS-PAGE. Coomassie Brilliant Blue (CBB) was used to color the gel, and the molecular weight of the protein was determined using PM2700. A total of 9

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31

Sun, Wei, Yunying Han, and Kui Jiao. "Voltammetric albumin quantification based on its interaction with carminic acid." Journal of the Serbian Chemical Society 71, no. 4 (2006): 385–96. http://dx.doi.org/10.2298/jsc0604385s.

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In a weak acidic Britton-Robinson (B-R) buffer of pH 4.0, human serum albumin (HSA) can react rapidly with carminic acid (CAA) to form a supramolecular complex. Microelectrostatic fields in the molecular structure of HSA cause the electrostatic binding reaction of the positively charged CAA with the negatively charged HSA. CAA has a sensitive, second order derivative linear sweep voltammetric reductive peak at - 0.54 V (vs. SCE) on a dropping mercury electrode (DME). After the addition of HSA to a CAA solution, the reductive peak current of CAA decreased without a shift of the peak potential.

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32

Wang, Fangfang. "Determination of lignin concentration in bleaching effluent via Coomassie brilliant blue G-250 method." BioResources 15, no. 1 (2019): 228–39. http://dx.doi.org/10.15376/biores.15.1.228-239.

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Kraft pulp and alkali peroxide mechanical pulp were prepared with aspen and wheat straw and bleached with chlorine dioxide, an alkali extraction strengthened by hydrogen peroxide, hydrogen peroxide, or peroxyacetic acid. Eight different bleaching effluents were obtained, and a Coomassie brilliant blue G-250 method was applied to determine the lignin content in each of the bleaching effluents. The visible light spectra indicated that the alkali-soluble lignin and the alkali bleaching effluent could increase the absorbance of Coomassie brilliant blue G-250 at 640 nm, but the acidic soluble ligni

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33

Gersten, Douglas M., Pamela H. Wolf, and Edward J. Zapolski. "Differences in protein staining by Coomassie Brilliant Blue and neutron activated Coomassie Brilliant Blue dyes." Electrophoresis 8, no. 12 (1987): 545–51. http://dx.doi.org/10.1002/elps.1150081202.

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34

Lohner-Schurig, Sigrun, Ralf Stelzer, and Ahlert Schmidt. "Phytoplankton Staining Using Coomassie Brilliant Blue G." Internationale Revue der gesamten Hydrobiologie und Hydrographie 78, no. 1 (1993): 169–71. http://dx.doi.org/10.1002/iroh.19930780120.

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35

Sabullah, Khalizan, S. A. Ahmad, Fisal Ahmad, Siti Aimi Farah Zainal Abidin, Azlan Jualang Gansau, and Mohd Rosni Sulaiman. "Comparison of staining methods for two dimensional electrophoresis gel resolved with <i>Puntius javanicus</i> liver proteome." Journal of Biochemistry, Microbiology and Biotechnology 2, no. 1 (2014): 27–31. http://dx.doi.org/10.54987/jobimb.v2i1.127.

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The aim of this study was to compare the various staining methods based on coomassie briliant blue and silver nitrate stain for the two-dimensional gel electrophoresis resolved with Puntius javanicus liver proteome. The staining methods were selected base on the previous report about their compatibility with the mass spectrometry analysis. Silver staining method is known as the most sensitive method to visualize the maximum number of protein spots resolved in 2D gel but it is less sensitive(incompatible) toward mass spectrometry detection. Results of this study showed that a modified staining

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36

Almeida, Layane Rodrigues, João Sammy Nery Souza, Edson Cavalcanti Silva Filho, and Josy Anteveli Osajima. "Photocatalysis of Coomassie Brilliant Blue Using Clay Mineral." Materials Science Forum 869 (August 2016): 765–67. http://dx.doi.org/10.4028/www.scientific.net/msf.869.765.

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The presence of organic pollutants, which cannot be eliminated by conventional processes of primary and secondary treatment, can be problematic. Photocatalytic processes offer an efficient breakdown of organic pollutants into non-toxic compounds such as CO2 and H2O. This paper proposes the use of the titanium dioxide embedded in palygorskite as a photoactive material in the degradation of cationic dye, Coomassie Brilliant Blue. The system was irradiated using UV light for a maximum time of 120 minutes. The concentration of the dye used was 1.0x10-4 mol L-1 in 0.5 g L-1 of the photoactive mater

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37

Liang, Aihui, Zujun Lu, Qingye Liu, Xinghui Zhang, Guiqing Wen, and Zhiliang Jiang. "SERS quantitative analysis of trace HSA with a Coomassie brilliant blue G-250 molecular probe in nanogold sol substrate." RSC Advances 5, no. 8 (2015): 5711–15. http://dx.doi.org/10.1039/c4ra11778f.

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38

RAUF, M., S. ASHRAF, and S. ALHADRAMI. "Photolytic oxidation of Coomassie Brilliant Blue with HO." Dyes and Pigments 66, no. 3 (2005): 197–200. http://dx.doi.org/10.1016/j.dyepig.2004.09.006.

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39

Cao, Yungang, Jing Zhao, and Youling L. Xiong. "Coomassie Brilliant Blue-binding: a simple and effective method for the determination of water-insoluble protein surface hydrophobicity." Analytical Methods 8, no. 4 (2016): 790–95. http://dx.doi.org/10.1039/c5ay02630j.

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A novel Coomassie Brilliant Blue-binding method, which correlated well with the widely accepted ANS fluorescence method (R = 0.95), was developed to determine the surface hydrophobicity of water-insoluble proteins.

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40

Lievens, M. M., and Y. I. Ambroes. "Threshold of pathological proteinuria measured with Coomassie Brilliant Blue." Clinical Chemistry 31, no. 1 (1985): 163–64. http://dx.doi.org/10.1093/clinchem/31.1.163a.

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41

Bukallah, Saeed B., M. A. Rauf, and S. Salman Ashraf. "Photocatalytic decoloration of Coomassie Brilliant Blue with titanium oxide." Dyes and Pigments 72, no. 3 (2007): 353–56. http://dx.doi.org/10.1016/j.dyepig.2005.09.016.

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42

MOCHIZUKI, Y., and K. FURUKAWA. "Application of Coomassie brilliant blue staining to cultured hepatocytes." Cell Biology International Reports 11, no. 5 (1987): 367–71. http://dx.doi.org/10.1016/0309-1651(87)90003-8.

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43

Syrovy, Ivo. "Decreased coomassie brilliant blue colour yield with glycated proteins." Journal of Biochemical and Biophysical Methods 25, no. 1 (1992): 75–78. http://dx.doi.org/10.1016/0165-022x(92)90038-c.

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44

Kielkopf, Clara L., William Bauer, and Ina L. Urbatsch. "Variations of Staining Sodium Dodecyl Sulfate–Polyacrylamide Gels with Coomassie Brilliant Blue." Cold Spring Harbor Protocols 2021, no. 12 (2021): pdb.prot102236. http://dx.doi.org/10.1101/pdb.prot102236.

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Many variations of the original Coomassie Brilliant Blue staining procedure are in use. This protocol describes some selected variations on the standard procedure that give comparable and consistent staining results for proteins in the 20- to 200-kDa range.

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45

Wong, W. K., G. E. Wieringa, Z. Stec, et al. "A Comparison of Three Procedures for the Detection of Bence–Jones Proteinuria." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 34, no. 4 (1997): 371–74. http://dx.doi.org/10.1177/000456329703400406.

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A traditional electrophoretic procedure for detection of Bence–Jones proteinuria, employing Amido black stain on 200-fold concentrated urine, has been compared to two procedures employing highly sensitive protein stains not requiring prior urine concentration. All three procedures were carried out on 80 random urine samples screened for Bence–Jones proteinuria and 10 samples were provided by patients attending a myeloma clinic. A new procedure employing modified Coomassie brilliant blue stain on unconcentrated urine showed comparable sensitivity to the established procedure (82% versus 88%, re

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46

Bongertz, Vera. "Elution of proteins from polyacrylamide eels: a simple and economic procedure." Revista do Instituto de Medicina Tropical de São Paulo 31, no. 1 (1989): 44–47. http://dx.doi.org/10.1590/s0036-46651989000100009.

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A simplified methodology for the quantitative electroelution of proteins from polyacrylamide gels is described. After staining with Coomassie Brilliant Blue R 250, the identified bands are excised from the gel and the proteins eluted using a procedure developed for use in conventional tube gel electrophoresis equipment.

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47

Dhananasekaran, Solairaj, Rameshthangam Palanivel та Srinivasan Pappu. "Adsorption of Methylene Blue, Bromophenol Blue, and Coomassie Brilliant Blue by α-chitin nanoparticles". Journal of Advanced Research 7, № 1 (2016): 113–24. http://dx.doi.org/10.1016/j.jare.2015.03.003.

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48

Hofmann, W., S. Hoffmann, and G. E. Hoffmann. "Temperature dependence of the absorption spectrum of Coomassie Brilliant Blue." Clinical Chemistry 32, no. 10 (1986): 1989. http://dx.doi.org/10.1093/clinchem/32.10.1989.

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49

Foster, Chris. "Three Colors: Coomassie Brilliant Blue, Sudan I and Somalia Yellow." Leonardo 44, no. 1 (2011): 86–87. http://dx.doi.org/10.1162/leon_a_00101.

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By taking the lab into the studio, the artist describes in this article the first use of industrial chemical dyes with his paintings or dye-paintings. A brief explanation of this technique in art and the production process is given, together with a short introduction and history on chemical dyes, their toxicity and pigments.

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50

Valsalamilka, B., G. Sreekumar, C. I. Muneera, Kaladevi Sendhil, and C. Vijayan. "Nonlinear refraction of Coomassie brilliant blue dye in PVA matrix." Journal of Materials Science 40, no. 3 (2005): 777–78. http://dx.doi.org/10.1007/s10853-005-6322-9.

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