نتایج جستجو برای: lipofectamine

تعداد نتایج: 646  

Journal: :BMC Biotechnology 2006
Debra McLaggan Noppadon Adjimatera Kristina Sepčić Marcel Jaspars David J MacEwan Ian S Blagbrough Roderick H Scott

BACKGROUND Haplosclerid marine sponges produce pore forming polyalkylpyridinium salts (poly-APS), which can be used to deliver macromolecules into cells. The aim of this study was to investigate the delivery of DNA, siRNA and lucifer yellow into cells mediated by poly-APS and its potential mechanisms as compared with other lipofection systems (lipofectamine and N4,N9-dioleoylspermine (LipoGen))...

2013
Ekaterina A. Durymanova Ono Keila Iamamoto Juliana G. Castilho Pedro Carnieli Rafael de Novaes Oliveira Samira M. Achkar Maria L. Carrieri Ivanete Kotait Paulo E. Brandão

Rabies is a zoonotic disease that affects all mammals and leads to more than 55,000 human deaths every year, caused by rabies virus (RABV) (Mononegavirales: Rhabdoviridae: Lyssavirus). Currently, human rabies treatment is based on the Milwaukee Protocol which consists on the induction of coma and massive antiviral therapy. The aim of this study was to assess the decrease in the titer of rabies ...

Journal: :iranian journal of immunology 0
padideh ebadi department of biology, science and research branch, islamic azad university (iau) mohammad hossein karimi department of immunology and biochemistry, school of medical sciences, tarbiat modares university ali akbar pourfathollah department of immunology and biochemistry, school of medical sciences, tarbiat modares university saheb ghadam lotfi department of immunology and biochemistry, school of medical sciences, tarbiat modares university zahra soheila soheili department of biochemistry, institute of genetic engineering and biotechnology shahram samiee iranian blood transfusion organization research center smerdis hajati

background: dendritic cells (dcs) are ideal accessory cells in the field of gene therapy. delivery of dna and sirna into mammalian cells is a useful technique in treating various diseases caused by single gene defects. selective gene silencing by small interfering rnas (sirnas) and antisense oligodeoxynucleotides (odn)s is an efficient method for the manipulation of cellular functions. an effic...

2012
Tuck-yun Cheang Bing Tang An-wu Xu Guang-qi Chang Zuo-jun Hu Wei-ling He Zhou-hao Xing Jian-bo Xu Mian Wang Shen-ming Wang

Nanoparticles have an enormous potential for development in biomedical applications, such as gene or drug delivery. We developed and characterized aminopropyltriethoxysilane-functionalized silicon dioxide nanoparticles (APTES-SiNPs) for gene therapy. Lipofectamine(®) 2000, a commonly used agent, served as a contrast. We showed that APTES-SiNPs had a gene transfection efficiency almost equal to ...

2013
Shaohui Cui Shubiao Zhang Huiying Chen Bing Wang Yinan Zhao Defu Zhi

In this paper, the relatived mechanism between lipofectamine 2000 mediated transmembrane gene delivery and endocytic pathway were investigated. Clathrin and caveolae-mediated endocytic pathway contributions to transfection efficiency were studied. The inhibitors of endocytosis were used to treat HEp-2 cells before lipofectamine 2000/pGFP-N2 transfection. Transfection efficiency was evaluated wi...

2014
Ali Teimoori Hoorieh Soleimanjahi Manoochehr Makvandi

BACKGROUND Rotavirus (RV) is a major cause of gastroenteritis in infants and children and is one of the most severe public health problems. Rotaviruses outer layer contains two proteins including VP4 and VP7. These proteins are necessary for host-cell binding and penetration. TLP (triple layer virus particle) of RV is a complete infectious virion that binds to the target cells and internalized ...

Journal: :Journal of microbiology and biotechnology 2011
Soo-Jin Lee Sung-Hwa Yoon Kyung-Oh Doh

Cationic liposomes have been actively used as gene delivery vehicle because of their minimal toxicity, but their relatively low efficiency of gene delivery is the major disadvantage of these vectors. Recently, cysteine residue incorporation to HIV-1 Tat peptide increased liposomemediated transfection compared with unmodified Tat peptide. Therefore, we designed a novel modified Tat peptide havin...

Journal: :BioTechniques 2017
Kazuhiro Ishiguro Osamu Watanabe Masanao Nakamura Takeshi Yamamura Masanobu Matsushita Hidemi Goto Yoshiki Hirooka

Commercially available lipid-based transfection reagents are widely used to deliver DNA to cells. However, these lipid-based transfection reagents show poor gene transfer efficiency in primary cells. Here, we demonstrate a simple method to improve gene transfer efficiency in primary fibroblasts and hepatoblasts using a combination of lipid-based transfection reagents. Our data show that combine...

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