Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fudu Miao"'
Autor:
Brian J. Green, George Moonsammy, Stephen J. Streatfield, Vidadi Yusibov, Fudu Miao, Mark Stow, R. Mark Jones, Jessica A. Chichester
Publikováno v:
Viruses, Vol 4, Iss 11, Pp 3227-3244 (2012)
Recently, we have reported [1,2] on a subunit influenza vaccine candidate based on the recombinant hemagglutinin protein from the A/Indonesia/05/2005 (H5N1) strain of influenza virus, produced it using ‘launch vector’-based transient expression t
Externí odkaz:
https://doaj.org/article/6b01edc70c4a4898a2f586e845ace3d2
Publikováno v:
Journal of Polymers and the Environment. 6:31-41
Polylactic acid (PLA) is a hydrolytically degradable aliphatic polyester. The rate of polymer hydrolysis increases with time, and that has been attributed to the high reactivity of the terminal ester and the kinetics of autocatalysis. Hydrolysis is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1398872a7ba062c00602d4aa446667ae
https://doi.org/10.1023/a:1022826528673
https://doi.org/10.1023/a:1022826528673
Autor:
Jessica A. Chichester, Fudu Miao, Mark Stow, Stephen J. Streatfield, Brian J. Green, R. Mark Jones, Vidadi Yusibov, George Moonsammy
Publikováno v:
Viruses
Viruses; Volume 4; Issue 11; Pages: 3227-3244
Viruses, Vol 4, Iss 11, Pp 3227-3244 (2012)
Viruses; Volume 4; Issue 11; Pages: 3227-3244
Viruses, Vol 4, Iss 11, Pp 3227-3244 (2012)
Recently, we have reported [1,2] on a subunit influenza vaccine candidate based on the recombinant hemagglutinin protein from the A/Indonesia/05/2005 (H5N1) strain of influenza virus, produced it using 'launch vector'-based transient expression techn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51ca080d502c6e2af81591f0028fd8a9
https://pubmed.ncbi.nlm.nih.gov/23202523
https://pubmed.ncbi.nlm.nih.gov/23202523
Autor:
Dhinakar S. Kompala, Fudu Miao
Publikováno v:
Biotechnology and Bioengineering. 42:74-80
A two-stage culture strategy was studied for continuous high-level production of a foreign protein in the chemically inducible T7 expression system. The first stage is dedicated to the maintenance of plasmid-bearing cells and the second stage to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f807d4294f9a265e8c8b070225c4385
https://doi.org/10.1002/bit.260420110
https://doi.org/10.1002/bit.260420110
Publikováno v:
Biotechnology Progress. 9:153-159
Phage lambda infection was investigated for possible production of toxic foreign proteins in Escherichia coli. The target gene transcription was regulated by a T7 promoter, which was initiated under the action of T7 RNA polymerase delivered by infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9679350e49c1bb0d9c314d21ed724df
https://doi.org/10.1021/bp00020a006
https://doi.org/10.1021/bp00020a006
Autor:
Michael Felo, Jaclyn Shervin, Elsie DiBella, Patricia Alred, Ajoy Velayudhan, Mark Teeters, Fudu Miao
Publikováno v:
Biotechnology progress. 25(4)
Diafiltration of a protein solution into a new buffer is a common final step in biopharmaceutical manufacturing. However, the excipient concentrations in the retentate are not always equal to their corresponding concentrations in the new buffer (diaf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c38b1d0f846b4ca0104942ba5b6c703
https://pubmed.ncbi.nlm.nih.gov/19569193
https://pubmed.ncbi.nlm.nih.gov/19569193
Publikováno v:
Biotechnology and bioengineering. 42(6)
A flow cytometric method was developed for the assay of beta-galactosidase in single Escherichia coli cells. A new fluorogenic substrate for beta-galactosidase, C(12)FDG, contains a lipophilic group that allows the substrate to penetrate through cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3cb3d7459d2583410bd1def256f42b4
https://pubmed.ncbi.nlm.nih.gov/18613103
https://pubmed.ncbi.nlm.nih.gov/18613103
Autor:
Dhinakar S. Kompala, Fudu Miao
Publikováno v:
Biotechnology and bioengineering. 40(7)
A novel Eschericha coli expression system directed by bacteriophage T7 RNA Polymerase utilized for overexpression of the cloned gene. The recombinant cell contains the plasmid with a bacteriophage promoter, the T7 promoter, to regulate the expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f8af5d0110ab4f2ea4fc3d9018335ce
https://pubmed.ncbi.nlm.nih.gov/18601182
https://pubmed.ncbi.nlm.nih.gov/18601182
Publikováno v:
In Desalination 1985 56:355-366