独白
发表于 2025-3-28 18:25:55
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Rankle
发表于 2025-3-28 20:20:13
Recombinant CHO Cell Pool Generation Using PiggyBac Transposon System,re, we describe the generation of CHO cell pools using the piggyBac transposon system for mediating gene integration. The method describes the co-transfection of cells with the donor plasmid (coding for the gene of interest) and the helper plasmid (coding for the transposase) using polyethyleneimine
BOON
发表于 2025-3-29 01:14:47
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道学气
发表于 2025-3-29 05:50:59
Expression of Multispecific Antibodies,the increased complexity (e.g., the interface design and the presence of multiple binders), such molecules are generally more challenging to express and purify compared to standard monoclonal antibodies (mAbs). We describe here an optimized methodology to express and purify basic bispecific antibodi
Influx
发表于 2025-3-29 09:45:11
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Nefarious
发表于 2025-3-29 13:48:25
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Devastate
发表于 2025-3-29 19:07:14
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匍匐前进
发表于 2025-3-29 21:25:24
Application of the CRISPR/Cas9 Gene Editing Method for Modulating Antibody Fucosylation in CHO Cellove both the productivity of recombinant cell lines as well as the quality of therapeutic antibodies. Antibody glycosylation is a critical quality attribute for therapeutic biologics because the glycan patterns on the antibody fragment crystallizable (Fc) region can alter its clinical efficacy and s
周兴旺
发表于 2025-3-30 03:00:41
Development of Responsive Promoters and their Utilization for Stable CHO Sensor Cell Lines,f the desired molecule, it is important to monitor and adjust bioprocess parameters like oxygen concentration as well as osmolality. However, the observation of crucial cultivation parameters can be an elaborate procedure requiring lots of hands-on work. In addition, for emerging modeling approaches
机密
发表于 2025-3-30 06:54:33
CRISPR Deletion of miR-27 Impacts Recombinant Protein Production in CHO Cells,lly hundreds of target genes. In that regard, their utility has been demonstrated as a strategy to improve the cellular phenotypes important in the biomanufacturing of recombinant proteins. Common approaches to stably deplete miRNAs are the use of sponge decoy transcripts or shRNA inhibitors, both o