Search results for "MAB purification" in Articles / App Notes

Article Comparing Protein A Resins for Monoclonal Antibody Purification
As a consequence, downstream processing must accept and handle higher titers of mAbs in harvested cell-culture fluid (HCCF), and vendors of mAb purification technologies must develop chromatography re…

Article The Development and Application of a Monoclonal Antibody Purification Platform
Early Platform Description The MAb purification platform used by Pfizer for early-phase clinical supplies has evolved over the last five years to accommodate increases in titer and associated i…

Article New Therapies Present Scaling Challenges
The downstream purification process can be scaled up, as the purification process for a gene therapy can use similar hardware as is used in mAb purification.  “In general, purification processe…

Article Process Chromatography: Continuous Optimization
He adds that they are also commonly used in polishing steps during mAb purification. Multimodal resins most often separate molecules based on ligand properties, but there are examples of multimoda…

Article HT Multi-Product Liquid Chromatography for Characterization of Monoclonal Antibodies
If used correctly, these new analytical methods can reduce analysis and product development time. ABSTRACT Monoclonal antibodies represent a significant portion of sales in the biopharma…

Article Development of Purification for Challenging Fc-Fusion Proteins
…of commercial mAbs (6-10), which typically consist of two or three chromatographic column steps for mAb purification that allow for the purification of similar molecules with minimal development and …

Article Defining Critical Quality Attributes for Monoclonal Antibody Therapeutic Products
An approach for establishing the CQAs of a mAb product by evaluating impact and uncertainty during risk assessment. A critical quality attribute (CQA) has been defined as “a physical, chemical, …

Article Antibody Production in Microbial Hosts
The authors review the status of expression of antibodies in microbial hosts and present the recent advances in the production of aglycosylated antibodies in bacteria. By Anurag S. Rathore, Jyot…

Article Preclinical Evaluation of Product Related Impurities and Variants
The key steps included collecting fractions during the mAb purification, assessing the charged species in each sample using the analytical CEX method, and performing cell potency assay on these sample…

Article Re-use of Protein A Resin: Fouling and Economics
Mar 01, 2015 By Anurag S. Rathore, Mili Pathak, Guijun Ma, Daniel G. Bracewell BioPharm International Volume 3, Issue 28 In the past two decades, Protein A affinity chromatography ha…

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