نتایج جستجو برای: cho cell mutant

تعداد نتایج: 1770578  

Journal: :modares journal of medical sciences: pathobiology 2013
azam rahimpour behrouz vaziri farzaneh barkhordari leila nematollahi ahmad adeli

objective: development of high producing mammalian cell lines is a major bottleneck in manufacturing of recombinant therapeutic proteins. this study examines the effect of using the matrix attachment region from the human interferon beta gene in combination with promoter activation strategy with e1a 13s protein on human tissue plasminogen activator (t-pa) expression in chinese hamster ovary (ch...

2001
Lei Wei FranCois Alhenc-Gelas Florent Soubrier Annie Michaud Pierre Corvol Eric Clauser

Chinese hamster ovary (CHO) cells have been transfected with either a full-length cDNA encoding human angiotensin I-converting enzyme (kininase 11; EC 3.4.15.1) (ACE) or a mutated cDNA, in which the last C-terminal 47 amino acids, including the putative transmembrane domain, are not translated. Cell lines expressing high levels of the wild-type ACE or the mutant were established. The cells tra...

Journal: :The Journal of Cell Biology 2005
Claudia Seelenmeyer Sabine Wegehingel Ivo Tews Markus Künzler Markus Aebi Walter Nickel

Galectin-1 is a component of the extracellular matrix as well as a ligand of cell surface counter receptors such as beta-galactoside-containing glycolipids, however, the molecular mechanism of galectin-1 secretion has remained elusive. Based on a nonbiased screen for galectin-1 export mutants we have identified 26 single amino acid changes that cause a defect of both export and binding to count...

Journal: :cell journal 0
kianoush dormiani yahya khazaie mahboobeh forouzanfar kamran ghaedi mohammad reza mofid khadijeh karbalaie

background: the aim of this study was to produce a stable cho cell line expressing tenecteplase. materials and methods: in the first step, the tenecteplase coding sequence was cloned in a pdb2 vector containing attb recognition sites for the phage φc31 integrase. then, using lipofection, the cho cells were co-transfected with constructed recombinant plasmid encoding tenecteplase and attb recogn...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1985
O Kuge M Nishijima Y Akamatsu

Mutant clones of Chinese hamster ovary (CHO) cells defective in the base-exchange reaction of phospholipids with choline were isolated by using an in situ enzymatic assay for the reaction in cell colonies immobilized on polyester cloth. The specific activities of the choline-exchange reaction in extracts of one of the mutants (designated 64) grown at 33 degrees C and 40 degrees C were 13% and 6...

Journal: :novelty in biomedicine 0
zeinab soleimanifar cellular and molecular biology research center, shahid beheshti university of medical sciences mojgan bandehpour department of biotechnology ,school of advanced technologies in medicine, shahid beheshti university of medical sciences bahram kazemi department of biotechnology ,school of advanced technologies in medicine, shahid beheshti university of medical sciences

background: luteinizing hormone (lh) was secreted by the stimulating cells of the testes and ovaries in the anterior pituitary gland. the application of this hormone is in the treatment of men and women with infertility and amenorrhea respectively. m aterials and methods: in the present study the alpha and beta subunits of human lh gene were cloned into the pegfp-n1 expression vector and produc...

Whole-cell pertussis vaccine (wP) has been imperative and highly effective in preventing childhood deaths due to pertussis. Pertussis toxin is one of the virulence factors of Bordetella pertussis in all available pertussis vaccines. wP production in Razi Vaccine and Serum Research Institute is according to bioreactor culture of B. pertussis strains in B2 medium. The aim ...

Journal: :iranian journal of biotechnology 2009
mahboobe ghaedi abbas sahebghadam lotfi masoud soleimani mehdi shamsara sare arjmand

in this study, in order to facilitate and accelerate the production of eukaryotic protein alpha 1-antitrypsin (aat) with correct post-translational modifications, a protein production system based on the transduction of cho and cos-7 cells using lentiviral vectors was developed. human aat cdna was cloned into a replication-defective lentiviral vector. the transgene aat-jred chimer was transferr...

Abbas Sahebghadam Lotfi, Behzad Adibi Mahboobe Ghaedi Masoud Soleimani, Mehdi Shamsara Sare Arjmand

In this study, in order to facilitate and accelerate the production of eukaryotic protein alpha 1-antitrypsin (AAT) with correct post-translational modifications, a protein production system based on the transduction of CHO and COS-7 cells using lentiviral vectors was developed. Human AAT cDNA was cloned into a replication-defective lentiviral vector. The transgene AAT-Jred chimer was transferr...

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