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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Exp Gerontol ; Overcoming the nuclear barrier: Medium was removed from the cells, replaced with complexes, and incubated. L—L [ PubMed ]. Cancer Gene Ther ; 8: Where a ratio was tested more than once, the mean transfection efficiency is plotted.
Journal List J Biomol Tech v. J Cell Sci ; Currie1 Bridget A. EGFP gene expression allows easy determination of the proportion of cells that is gene-modified protockl a single-cell basis, detecting the number of cells expressing EGFP and their level of EGFP expression via flow cytometry.
Modification of adenovirus gene transfer vectors with synthetic polymers: Hunt1 Margaret J. Fluorescence produced by transfection reagents can be confused with green fluorescent proteins in mammalian cells. Burlington, Lipofedtamine, Canada 9. Here, we describe the comparison of transfection of HUVEC using nine chemical transfection reagents, currently commercially available, to identify the reagent that elicits the highest transfection efficiency without compromising cell viability.
The complexes were added directly to cells in 2 mL complete medium and incubated. National Center for Biotechnology InformationU. Optimization of transfection of human endothelial cells. A transfection reagent with a high transfection efficiency and low cytotoxicity was sought to retain sufficient viability of transfected HUVEC protoco, subsequent assays.
siRNA transfection in endothelial cells – siRNA, microRNA and RNAi
Polymers for DNA delivery. Green fluorescent protein as a novel tool to lipofdctamine apoptosis and necrosis. Infect Immun ; J Biol Chem ; The complexes were added to cells in 2 mL complete medium and incubated. Hum Gene Ther ; Comparison of the efficiency and safety of non-viral vector-mediated gene transfer into a wide range of human cells.
Culture of human endothelial cells derived from umbilical veins. An equal volume of PLUS reagent was added. Lipofectamine LTX was added, and lipofectwmine complexes were allowed to form by incubation for 25 min.
Abstract Primary cells, such as HUVEC, are notoriously difficult to transfect and are susceptible to the toxic effects of transfection reagents.
BoxChristchurchNew Zealand Phone: Other studies have reported differences in cell characteristics between HUVEC from single or multiple-pooled donors, 35 which may explain this variability.
Bioconjug Chem ; Reporter gene expression for monitoring gene transfer. Kreppel F, Kochanek S. This project was funded by the Cancer Society of New Zealand. Curr Drug Deliv ; 1: Our study demonstrated that a small selection of commercially available chemical transfection reagents was able to transfer exogenous genes efficiently to primary human cells.
Front Biosci ; 7: It has been reported that some cationic liposome transfection reagents could lead to autofluorescence in fluorescent microscopy and flow cytometry analysis, 38 but our results for mock transfection using Lipofectamine and Lipofectamine LTX showed no autofluorescence.
An electroporation protocol for efficient DNA transfection in PC12 cells.
On the other hand, luciferase activity, detected via conversion of protofol substrate, resulting in amplified signal, determines the behavior of the entire population, thereby losing information about single cells. This study analyzed nine currently available, commercial transfection reagents prorocol showed that cationic lipid reagents were the most efficient in gene-modifying HUVEC. Highly efficient transduction of endothelial cells by targeted artificial virus-like particles.
Biotechnol Prog ; HUVEC have a limited lifespan and a relatively low proliferation rate.