TransFect Protocol Database. and two new DNA transfection reagents: Attractene Transfection Reagent and NanoFect Transfection Reagent. I tried Lipofectamine and Attractene which both had a bad efficiency. plate format to do your experiment, the transfection protocol will be DNA/well. 年7月29日 QIAGEN Supplementary Protocol Protocol: Fast?Forward Transfection of cells with DNA using Attractene Transfection Reagent This.

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Cell strategies for high transfection efficiency

Don’t have an account? In this protocol, cell plating and transfection are performed on the same day. For this reason, further optimization is recommended to achieve maximum transfection efficiency. The latest reagents use advanced technology to meet all DNA transfection needs. Rather than adapting existing protocols to fit the cell type, the TransFect Database enables researchers to access exactly the protocol needed by simply entering the attracten type, nucleic acid, and plate format into the online system.

As a general rule, optimization of transfection can be performed by varying DNA and Attractene Reagent amount as follows: If you require a thermal cycler that delivers high performance and high throughput, while still ret….

Prime thermal cyclers provide flexible PCR Added: As a starting point, we recommend using 6-well plate? In addition, the absence of lipids makes this reagent suitable for lipid or signal transduction research.


For these reasons, it is ideal for use when protocop of animal-derived components is a priority, for example, in biopharmaceutical applications.

Incubate the samples for 10? Make money from your old lab equipment.

Routing Protocol vs Ro Home PCR Cell strategies for high tr The effect of using greater or lesser amounts of DNA and Attractene Transfection Reagent can be observed using these combinations. For stable transfections, passage cells into the appropriate selection medium 24? Cell strategies for high transfection efficiency 19 Feb by Qiagen. Hygiena expands with PCR-based systems to cover the entire contamination detection spectrum Added: Incubate the cells with the transfection complexes under their normal growth conditions and monitor gene expression after an appropriate time e.

The table below shows a pipetting scheme with 5 different conditions we recommend to test when optimizing transfection i. To complement and enhance the existing portfolio of trusted transfection solutions, Qiagen has launched the TransFect Protocol Database and two new DNA transfection reagents: Absence of animal-derived components also attrqctene regulatory compliance. The optimal incubation time for gene expression analysis depends on the cell type, the gene expressed, and the method of analysis.

The amounts given are for one well of a 6-well plate. The amount of transfection reagent and DNA required for optimal performance may vary, depending on the cell line and gene target. Transfection optimization Optimizing DNA 0.

The Fast-Forward Protocol, in which cell plating and transfection are performed on the same day, has been shown to work successfully with a wide variety of cell types. Maintain cells in attrwctene culture medium until colonies appear. Use of the TransFect Database is free of charge and no registration is required.


Cell strategies for high transfection efficiency | Laboratory Talk

Ease of handling means that Attractene Reagent is suitable for use with automated systems. However, for some cell types, especially difficult-to-transfect cells such as suspension cells and primary cells, higher transfection efficiencies may be achieved by plating cells 24 hours prior to transfection for a protocol, consult the Attractene Transfection Reagent Handbook at www.

Shortly before transfection, seed 3x cells per well of a 6-well plate in ? The instrument range of Hygiena International Ltd, experts in rapid microbial detection, monitoring….

Using Attractene Reagent also ensures exceptionally low cytotoxicity.

Simple Safe Parallel Reaction Sampling. NanoFect Reagent is completely chemically synthesised, free of animal-derived components, and has been tested for the absence of endotoxins. This reagent is suitable attracteme a range of transfection applications, including transient or stable transfection, transfection of shRNA short-hairpin RNA vectors, and DNA cotransfection. Cells may alternatively be seeded after step 3 of this protocol.