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Search Purification (Commentary)

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Results 1 - 8 of 8
EC Number Purification (Commentary)
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67-
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67native enzyme 14.91fold from rhizomes by ammonium sulfate fractionation, tert-butanol precipitation at 25°C and pH 7.0 using the interfacial precipitateand the aqueous phase, and ultrafiltration, method optimization
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67native enzyme from rhizomes by ammonium sulfate fractionation and dialysis
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67native enzyme from rhizomes by ammonium sulfate fractionation, anion exchange chromatography, SDS-PAGE, and gel filtration
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67native enzyme from rhizomes by saturation ammonium sulfate fractionation and anion exchange chromatography to homogeneity
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67partially purified 252fold with a recovery of 61%, ion exchange chromatography
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67purification via a three-phase partitioning system
Display the word mapDisplay the reaction diagram Show all sequences 3.4.22.67ultrasonic-assisted liquid-liquid microextraction of the proteases from ginger and sodom apple using natural deep eutectic solvents, NADES. Selective partitioning of NADES-assisted microextraction yields more protease in NADES-enriched top phase. Maximum yield is achieved with 25% (v/v) of NADES, 15% (w/v) of source concentration and ultrasound temperature and time as 35°C and 10 min, respectively
Results 1 - 8 of 8