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Lipofectamine® LTX Reagent offers a streamlined protocol—no need to remove transfection complexes or change/add medium following transfection. A simple. Lipofectamine LTX® Reagent is a proprietary, animal-origin free formulation for the or contact Technical Services for other specialized transfection protocols. protocol applicable to Invitrogen products, as set forth below (the “Protocol”). by adding 50 μL of Lipofectamine™ LTX to μL of Opti-MEM® medium.

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Endothelial cell COX-2 expression and activity in hypoxia. Nine chemical transfection reagents, currently commercially available, were compared for their ability to transfect HUVEC in vitro.

An electroporation protocol for efficient DNA transfection in PC12 cells.

Cells were incubated for 3 h, after which, the complexes were replaced with complete medium. Importantly, dead cells tend to detach from the growth surface and thus, were not analyzed in this study.

Cells can be gene-modified in vitro and prptocol vivo using physical, viral, or chemical methods. Differences in EGFP expression were dependent mainly on transfection reagent. J Pharm Sci ; Robinson1 and Gabi U.


An electroporation protocol for efficient DNA transfection in PC12 cells.

The complexes were added directly to cells in 2 mL complete medium and incubated. Cell viability after transfection.

Br J Haematol ; Exp Cell Res ; Hum Gene Ther ; Articles from Journal of Biomolecular Techniques: Br J Pharmacol ; Efficient gene transfer pdotocol human umbilical vein endothelial cells allows functional analysis of the human tissue factor gene promoter. Chemical transfection reagents have been shown to reduce growth and viability of cells after transfection, possibly as a llipofectamine of changes in the strength of the cell membrane.

Polymers for DNA delivery. Arch Biochem Biophys ; Optimal expression of transfected genes in vitro is influenced by many factors, including cell type, passage history, confluence, vector structure, size and purity, promoters, a DNA: The mixture was incubated for 5 min. Curr Gene Ther ; 4: Nonviral lipofecatmine for targeted delivery of plasmid DNA and oligonucleotide. Lipofectamine LTX was added, and the complexes were allowed to form by incubation for 25 min.

Journal List J Biomol Tech v. Therefore, measurement of EGFP expression by flow cytometry may underestimate the total number of cells that was gene-modified initially.


Differential ability of human endothelial cells to internalize and express exogenous DNA. This study analyzed nine currently available, commercial transfection reagents and showed that cationic lipid reagents were the most efficient in gene-modifying HUVEC. Where a ratio was tested more than once, the mean transfection efficiency is plotted.

Please review our privacy policy. Curr Opin Biotechnol ; 8: Physical methods of nucleic acid transfer: Highly efficient transduction of endothelial cells by targeted lipoffectamine virus-like particles. National Center for Biotechnology InformationU. Inhibition of hydrophobic protein-mediated Candida albicans attachment to endothelial cells during physiologic shear flow.

Mixtures were incubated for 5 min and then combined together for a further 20 min. Improving safety of gene therapy. BoxChristchurchNew Zealand Phone: