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anion exchange chromatography and gel-filtration
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by using affinity chromatography and gel filtration
cobalt immobilized metal-affinity column chromatography and Source 30Q column chromatography
K-12, using ammonium sulfate precipitation and column chromatography on Sephadex G-200 and DEAE-Sephadex A-50
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Ni-affinity chromatography
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Ni-affinity chromatography and anion exchange chromatography
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Ni-NTA column chromatography and gel filtration
partially, recombinant enzyme from Escherichia coli, 37fold
recombinant C-terminally His-tagged enzyme ASADH from Escherichia coli strain BL21(DE3) by nickel affinity and anion exchange chromatography, and dialysis
recombinant C-terminally His-tagged enzyme ASADH from Escherichia coli strain BL21(DE3) by nickel affinity chromatography, dialysis, and ultrafiltration
recombinant enzyme from Escherichia coli to over 95% purity by anion exchange chromatography and gel filtration
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recombinant enzyme from strain BL21(DE3) in several steps
recombinant His-tagged enzyme from Escherichia coli by nickel affinity and anion exchange chromatography, followed by ultrafiltration
recombinant His-tagged enzyme from Escherichia coli by nickel affinity chromatography to 96% purity
recombinant His-tagged enzyme from Escherichia coli strain M15 by nickel affinity chromatography and gel filtration
recombinant His-tagged wild-type and mutants from Escherichia coli strain BL21(DE3) by nickel affinity chromatography
using a Co2+ affinity matrix and anion exchange chromatography
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using ammonium sulfate precipitation and column chromatography on Q Sepharose XL and Procion Red-A
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using ammonium sulfate precipitation and column chromatography on Sephadex G-200, DEAE-cellulose and hydroxylapatite
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using anion-exchange chromatography, Source 15Q, followed by gel filtration
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using anionic exchange chromatography on DEAE EMD 650 column and Q-Sepharose column
using column chromatography on DEAE-cellulose, DEAE-Sephadex A-50, hydroxylapatite, ultrogel ACA-44 and Sepharose C3
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using column chromatography on Q Sepharose XL and omega-aminohexyl-agarose for the purification of V. cholerae I and column chromatography on Q Sepharose XL for the purification of V. cholerae II
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using column chromatography on Q Sepharose XL and phenyl-Sepharose
using heat treatment, acid precipitation, protamine sulfate treatment and ammonium sulfate precipitation
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using heat treatment, column chromatography on DEAE-cellulose, ammonium sulfate precipitation and column chromatography on Sephadex G-200
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using protamine sulfate treatment, ammonium sulfate precipitation, chromatography on DEAE-Sephadex A-50 column, Bio-Gel hydroxylapatite phosphate column, Bio-Gel hydroxylapatite sulfate column, acid treatment and column chromatography on Sephadex G-200
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