Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Burkhard, Wilms"'
Surface display vectors for selective detection and isolation of high level antibody producing cells
Autor:
Hans-Peter Knopf, Thomas Jostock, Sabine Lang, Johannes Wichter, Nommay Audrey Josiane, Delia Drewello, Burkhard Wilms
Publikováno v:
Biotechnology and Bioengineering. 113:2386-2393
Cell line generation for production of biopharmaceuticals in mammalian cells usually involves intensive screening of clones to identify the rare high producers. In order to facilitate efficient and selective fluorescence activated cell sorting (FACS)
Autor:
Holger Laux, Thomas Jostock, Anett Ritter, Joerg Schmidt, Burkhard Wilms, Mara Fornaro, Sandrine Romand
Publikováno v:
Biotechnology and Bioengineering. 113:1094-1101
Chinese Hamster Ovary (CHO) cells are widely used for the large-scale production of recombinant biopharmaceuticals. However, attempts to express IGF-1 (a mutated human Insulin-like growth factor 1 Ea peptide (hIGF-1Ea mut)) in CHO cells resulted in p
Autor:
Anett Ritter, Thomas Jostock, Sabine Geisse, Burkhard Wilms, Holger Laux, Johannes Wienberg, Bernd Voedisch
Publikováno v:
Biotechnology and Bioengineering. 113:1084-1093
Chinese Hamster Ovary (CHO) cells are widely used for large scale production of recombinant biopharmaceuticals. Although these cells have been extensively used, a demand to further increase the performance, for example, to facilitate the process of c
Surface display vectors for selective detection and isolation of high level antibody producing cells
Autor:
Sabine, Lang, Delia, Drewello, Johannes, Wichter, Audrey, Nommay, Burkhard, Wilms, Hans-Peter, Knopf, Thomas, Jostock
Publikováno v:
Biotechnology and bioengineering. 113(11)
Cell line generation for production of biopharmaceuticals in mammalian cells usually involves intensive screening of clones to identify the rare high producers. In order to facilitate efficient and selective fluorescence activated cell sorting (FACS)
Publikováno v:
BMC Proceedings
Background Chinese hamster ovary (CHO) cells are the most widely used host for large scale production of recombinant therapeutic proteins. A combination of several gene editing approaches applied to Novartis proprietary CHO cell line resulted in a su
Autor:
Anett, Ritter, Bernd, Voedisch, Johannes, Wienberg, Burkhard, Wilms, Sabine, Geisse, Thomas, Jostock, Holger, Laux
Publikováno v:
Biotechnology and bioengineering. 113(5)
Chinese Hamster Ovary (CHO) cells are widely used for large scale production of recombinant biopharmaceuticals. Although these cells have been extensively used, a demand to further increase the performance, for example, to facilitate the process of c
Autor:
Sandrine, Romand, Thomas, Jostock, Mara, Fornaro, Joerg, Schmidt, Anett, Ritter, Burkhard, Wilms, Holger, Laux
Publikováno v:
Biotechnology and bioengineering. 113(5)
Chinese Hamster Ovary (CHO) cells are widely used for the large-scale production of recombinant biopharmaceuticals. However, attempts to express IGF-1 (a mutated human Insulin-like growth factor 1 Ea peptide (hIGF-1Ea mut)) in CHO cells resulted in p
Publikováno v:
Applied Microbiology and Biotechnology. 55:750-757
The genes encoding hydantoinases (hyuH1) and carbamoylases (hyuC1) from Arthrobacter aurescens DSM 3745 and Arthrobacter aurescens DSM 3747 (hyuH2, hyuC2) were cloned in Escherichia coli and the nucleotide sequences determined. The hydantoinase genes
Autor:
Matthias Reuss, Burkhard Wilms, Martin Siemann, Ralf Mattes, Josef Altenbuchner, Achim Hauck, Christoph Syldatk
Publikováno v:
Biotechnology and Bioengineering. 73:95-103
A high-cell-density fed-batch fermentation for the production of heterologous proteins in Escherichia coli was developed using the positively regulated Escherichia coli rhaBAD promoter. The expression system was improved by reducing of the amount of
Autor:
Anja Wiese, Christoph Syldatk, Josef Altenbuchner, Ralf Mattes, Markus Pietzsch, Burkhard Wilms
Publikováno v:
Journal of Biotechnology. 68:101-113
An l -N-carbamoyl amino acid amidohydrolase ( l -N-carbamoylase) from Arthrobacter aurescens DSM 3747 was cloned in E. coli and the nucleotide sequence was determined. After expression of the gene in E. coli the enzyme was purified to homogeneity and