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Application note for the rapid analysis of adenoviruse type 5 particles with bio-monolith anion-exchange HPLC Columns
| Publication Part Number | 5990-5524EN | |||
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Anion-exchange chromatography for the analysis and purification of oligonucleotides using a PL-SAX column.
| Publication Part Number | 5990-8297EN | ||
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必威体育登录手机Small –scale purification of a monoclonal antibody from a cell lysate and the subsequent analysis on a single instrument, the Agilent 1260 Infinity Bio-inert Quaternary LC.
| Publication Part Number | 5991-1195EN | ||||
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This Application Note demonstrates the sensitive and reproducible analysis of N-linked glycans of human immunoglobulin G with a novel HILIC column and fluorescence detection.
| Publication Part Number | 5991-4801EN | |||
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This work describes a high flow LCMS method to demonstrate the high resolution mass analysis of mAbs with good chromatography and its utility in analysis of Biosimilar mAbs.
| Publication Part Number | 5991-4266EN | ||
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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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In this application note, pre-packed Bio-monolith Protein A columns, part of the AdvanceBio family, were used to demonstrate the quick capture of monoclonal antibody titer
| Publication Part Number | 5991-2990EN | ||
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必威体育登录手机The Agilent AdvanceBio Peptide Mapping column separates mAb tryptic digests at low system pressures, providing UHPLC performance from HPLC operating conditions.
| Publication Part Number | 5991-3585EN | |||
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Peptide mapping is the common analytical technique for characterizing biologic therapeutic proteins.
| Publication Part Number | 5991-3600EN | ||||
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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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Ion exchange is a commonly used technique for the separation of complex protein mixtures.
| Publication Part Number | 5990-9931EN | ||||
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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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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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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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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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Fast and efficient LC TOF/MS characterizes intact and digested IgG to identify glycoform masses and profiles.mAb-glyco chip analysis built a glycan accurate mass database.
| Publication Part Number | 5990-2323EN | ||||
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Accurate mass intact protein analysis using 6550 iFunnel Q-TOF
| Publication Part Number | 5991-2116EN | |||
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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This Application Note describes a high-resolution, pH-based separation of acidic and basic charge variants for monoclonal antibodies using the Agilent 1260 and BiomAb PEEK
| Publication Part Number | 5991-1407EN | ||
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必威体育登录手机Rapid reversed-phase separations of intact and reduced monoclonal antibodies (mAbs) were optimized using Agilent ZORBAX RRHD 300SB-C3 columns.
| Publication Part Number | 5990-9667EN | |||
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