Search results for "Bradford protein assay"

showing 4 items of 4 documents

Use of an enzyme-assisted method to improve protein extraction from olive leaves.

2013

The improvement of protein extraction from olive leaves using an enzyme-assisted protocol has been investigated. Using a cellulase enzyme (Celluclast® 1.5L), different parameters that affect the extraction process, such as the influence and amount of organic solvent, enzyme amount, pH and extraction temperature and time, were optimised. The influence of these factors was examined using the standard Bradford assay and the extracted proteins were characterised by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The optimum extraction parameters were: 30% acetonitrile, 5% (v/v) Celluclast® 1.5L at pH 5.0 and 55°C for 15min. Under these conditions, several protein extracts…

ChromatographybiologyChemistryPlant ExtractsSodiumExtraction (chemistry)Temperaturechemistry.chemical_elementGeneral MedicineCellulaseChemical FractionationAnalytical ChemistrySolventPlant LeavesElectrophoresisCellulaseOleaProtein purificationbiology.proteinElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisBradford protein assayFood SciencePlant ProteinsFood chemistry
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Efficient Extraction of Olive Pulp and Stone Proteins by using an Enzyme-Assisted Method

2014

An efficient protein extraction protocol for proteins from olive pulp and stone by using enzymes was developed. For this purpose, different parameters that affect the extraction process, such as enzyme type and content, pH, and extraction temperature and time, were tested. The influence of these factors on protein recovery was examined using the standard Bradford assay, while the extracted proteins were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The best extraction conditions were achieved at pH 7.0 and 5% (v/v) Palatase® 20000 L (lipase) for pulp and Lecitase® Ultra (phospholipase) for stone proteins. The optimal extraction temperature and time w…

Gel electrophoresisChromatographybiologyChemistryPulp (paper)Extraction (chemistry)engineering.materialElectrophoresisProtein purificationengineeringbiology.proteinLipasePolyacrylamide gel electrophoresisBradford protein assayFood ScienceJournal of Food Science
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Available Lysine in Protein, Assay Using o-Phthalaldehyde/ N-Acetyl-L-cysteine Spectrophotometric Method

1992

An assay was based on reaction of free e-amino groups in proteins with the o-phthalaldehyde/N-acetyl-L-cysteine reagent to form isoindoles, which absorb at 335 nm. The procedure was suitable for proteins or mixtures of proteins with available lysine contents of more than 5 moles lysine/mole protein and required absence of free amino acids and peptides. This method was simpler and more convenient than other methods, since it did not require hydrolysis, amino acid analysis, long heating periods or solvent extraction.

O-PhthalaldehydeHydrolysisChromatographyIsoindolesmedicine.diagnostic_testChemistrySpectrophotometryReagentLysineMolemedicineBradford protein assayFood ScienceJournal of Food Science
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Protein Quantitation: Bradford Method

2002

Protein quantitation according to the Bradford method. Keywords: protein quantitation; bradford; coomassie brilliant blue; calorimetric quantification

chemistry.chemical_compoundfluids and secretionsChromatographychemistryCoomassie Brilliant Blueparasitic diseasesQuantitative proteomicsequipment and supplieshuman activitiesBradford protein assayeLS
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