نتایج جستجو برای: recombinant plasmids

تعداد نتایج: 124414  

Journal: :Gene 1987
A Rethwilm G Darai A Rösen B Maurer R M Flügel

DNA of human spumaretrovirus (HSRV) was cloned from both cDNA and from viral DNA into phage lambda and bacterial plasmid vectors. The recombinant plasmids harboring viral DNA were characterized by Southern blot hybridization and restriction mapping. Physical maps were constructed from cDNA and found to be colinear with the restriction maps obtained from viral DNA. The recombinant clones isolate...

F. Ghazi F. Sorooshi M. Taghizadeh

  Parechoviruses form one of the nine genera in the picornaviridae family, and include two human pathogens: Human parechovirus type1 and 2 (Hpev1 and Hpev2). The genome of picornaviruses encodes a single polyprotein, which undergoes a cleavage cascade performed by virus encoded proteases to give the final virus proteins. The primary cleavage occurs by 2A protein and this step is critical for vi...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
T C He S Zhou L T da Costa J Yu K W Kinzler B Vogelstein

Recombinant adenoviruses provide a versatile system for gene expression studies and therapeutic applications. We report herein a strategy that simplifies the generation and production of such viruses. A recombinant adenoviral plasmid is generated with a minimum of enzymatic manipulations, using homologous recombination in bacteria rather than in eukaryotic cells. After transfections of such pla...

2013
Thorsten Gantke Sabrina Boussouf Julia Janzen Nicholas A. Morrice Steven Howell Elke Mühlberger Steven C. Ley

Activation of PKR (double-stranded-RNA-dependent protein kinase) by DNA plasmids decreases translation, and limits the amount of recombinant protein produced by transiently transfected HEK (human embryonic kidney)-293 cells. Co-expression with Ebola virus VP35 (virus protein 35), which blocked plasmid activation of PKR, substantially increased production of recombinant TPL-2 (tumour progression...

Journal: :jundishapur journal of microbiology 0
fatemeh fotouhi influenza research lab, department of virology, pasteur institute of iran, tehran, ir iran; influenza research lab, department of virology, pasteur institute of iran, , tehran, ir iran.tel/ fax: +98-2166496517 behrokh farahmand influenza research lab, department of virology, pasteur institute of iran, tehran, ir iran behnaz heidarchi influenza research lab, department of virology, pasteur institute of iran, tehran, ir iran maryam esghaei virology department, iran university of medical sciences, tehran, ir iran sima rafati molecular immunology and vaccine research lab, department of immunology, pasteur institute of iran, tehran, ir iran masoumeh tavassoti kheiri influenza research lab, department of virology, pasteur institute of iran, tehran, ir iran

background permanent antigenic variation of influenza viruses causes a major concern to develop an effective human influenza vaccine. conserved antigens are new vaccine candidates because it is not necessary to match the prepared vaccine with circulating strains. ion channel m2 protein is conserved among all influenza a viruses, allowing the virus to enter host cells. objectives to prepare an e...

Journal: :The Journal of Microbiology, Biotechnology and Food Sciences 2022

Polymerase of influenza virus is made up three subunits PB1, PB2, and PA, which are involved in viral genome transcription replication. Purification sufficient amounts polymerase essential to understand the catalytic function polymerase. In this study, we generated a expression system human embryonic kidney 293T cells (293T cells). The cDNAs for RNA segments 1, 2, 3, encode PA proteins, respect...

Journal: :Genetics and molecular research : GMR 2014
G X Wang L Hu Z Zhang D P Liu

The aim of this study was to construct an adenoviral expression vector for vascular endothelium growth factor 121 (VEGF121)-FLAG and humanized Renilla reniformis green fluorescent protein (hrGFP-1) genes, and to observe their expressions in bone marrow mesenchymal stem cells. Using pTG19T-VEGF121 as a template, polymerase chain reaction technology was adopted to mutate the VEGF121 gene by remov...

Journal: :Antimicrobial agents and chemotherapy 1974
G A Jacoby

Pseudomonas aeruginosa strain GN315, producing kanamycin acetyltransferase, can transmit a plasmid determining resistance to kanamycin, amikacin (BB-K8), butirosin, tobramycin, and sisomicin, but not gentamicin, to other pseudomonas strains. This plasmid, pMG5, belongs to the same incompatibility group as plasmids determining gentamicin resistance in P. aeruginosa via gentamicin acetyltransfera...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید