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必威体育登录手机This Application Note describes the quantification of human IgG with the Agilent Bio-Monolith Protein A HPLC Column with alternating column regeneration.
| Publication Part Number | 5991-4723EN | ||
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This shows the separation of four proteins by anion exchange chromatography using 4 different high salt-containing elution buffers (up to 2 M) for linear and step gradients.
| Publication Part Number | 5990-9614EN | |||||
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Ion exchange is a very useful technique to separate protein mixtures under mild conditions, most commonly by applying a shallow gradient of increasing salt concentration as el
| Publication Part Number | 5990-9629EN | |||
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Columns containing weak cation-exchange stationary phases offer a degree of versability when used for separation of positively charged proteins.
| Publication Part Number | 5990-9628EN | ||
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必威体育登录手机Agilent Bio MAb columns, in an Agilent 1260 Infinity Bio-inert Quaternary LC, characterize the charge heterogeneity of IgG1monoclonal antibody...
| Publication Part Number | 5991-0895EN | |||
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Ion exchange is a commonly used technique for the separation of complex protein mixtures.
| Publication Part Number | 5990-9931EN | ||||
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Column choice in SEC depends on column resolving range, identified by calibration with standards appropriate to analyte type, molecular weight range, and size in solution.
| Publication Part Number | 5991-2463EN | ||||
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必威体育登录手机Methods are given for the use of Agilent Bio-SEC columns, with LS, UV and RI detection, for quantification or quality control of protein aggregates
| Publication Part Number | 5991-1400EN | ||||
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必威体育登录手机Application note for the characterization of monoclonal antibodies on the Agilent 1260 Infinity Bio-inert Quaternary LC by SEC using the Agilent BioSEC columns
| Publication Part Number | 5990-6414EN | ||||
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