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pro vyhledávání: '"Esther Y C Koh"'
Autor:
Esther Y C Koh, Steven C L Ho, Mariati, Zhiwei Song, Xuezhi Bi, Muriel Bardor, Yuansheng Yang
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82100 (2013)
A set of mutated Encephalomyocarditis virus (EMCV) internal ribosome entry site (IRES) elements with varying strengths is generated by mutating the translation initiation codons of 10(th), 11(th), and 12(th) AUG to non-AUG triplets. They are able to
Externí odkaz:
https://doaj.org/article/32f5b977ccbd4f19ad7f48c227b8aa08
Publikováno v:
Bioengineered. 5:340-345
Maintaining high gene expression level during long-term culture is critical when producing therapeutic recombinant proteins using mammalian cells. Transcriptional silencing of promoters, most likely due to epigenetic events such as DNA methylation an
Autor:
Benjamin P. C. Soo, Mariati, Yuansheng Yang, Steven C. L. Ho, Sheng-Hao Chao, Esther Y. C. Koh
Publikováno v:
BMC Biotechnology
Background Methylated CpG dinucleotides in promoters are associated with the loss of gene expression in recombinant Chinese hamster ovary (CHO) cells during large-scale commercial manufacturing. We evaluated a promoter devoid of CpG dinucleotides, Cp
Publikováno v:
Biotechnology progress. 30(3)
The human cytomegalovirus promoter (hCMV) is susceptible to gene silencing in CHO cells, most likely due to epigenetic events, such as DNA methylation and histone modifications. The core CpG island element (IE) from the hamster adenine phosphoribosyl
Autor:
Zhiwei Song, Steven Hao-Kee Ho, Esther Y. C. Koh, Corrine Wan, Gavin Teo, Yuansheng Yang, Muriel Bardor, Miranda M. C. van Beers, Monika Mueller, Yen Wah Tong
Publikováno v:
Journal of Biotechnology
Journal of Biotechnology, Elsevier, 2013, 165 (3-4), pp.157-166. ⟨10.1016/j.jbiotec.2013.03.019⟩
Journal of Biotechnology, Elsevier, 2013, 165 (3-4), pp.157-166. ⟨10.1016/j.jbiotec.2013.03.019⟩
Immunoglobulin G (IgG), the most common class of commercial monoclonal antibodies (mAbs), exists as multimers of two identical light chains (LC) and two identical heavy chains (HC) assembled together by disulfide bridges. Due to the kinetics of mAb a