siRNA / miRNA gene silencing Human - U2OS DAXX

Gene silencing through the use of small interfering RNA (siRNA) has become a primary tool for identifying disease-causing genes. There are several aspects for preparing and delivering effective siRNA to knockdown a target gene. The length of siRNA should be 21–23nt long with G/C content 30–50%. If a validated siRNA sequence for your target gene is not available, use siRNA generated against the entire target gene ORF. Always work with two or three different siRNA constructs to get reliable results. If you are not sure how much siRNA to use for a given experiment, start with a transfection concentration of 10-50 nM and use siRNA-specific transfection reagent to ensure efficient siRNA delivery in a wide range of cells.

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Found 1 matching solution for this experiment

NM_001350

Sigma-Aldrich

Thermo Fisher Scientific

Upstream tips	Protocol tips	Downstream tips
Seed 2.5 × 10^5	Daxx siRNA: 5′-GGAGUUGGAUCUCUCAGAA Add diluted siRNA to diluted Lipofectamine® RNAiMAX Reagent (1:1 ratio).  Incubate for 5 minutes at room temperature and add to cells.  Incubate cells for 1day at 37°C and later transfect by electroporation with 2 μg of circularized wt HPV18 or wt HPV11 genome and incubate for another 48 h

Upstream tips
Seed 2.5 × 10^5
Protocol tips
Daxx siRNA: 5′-GGAGUUGGAUCUCUCAGAA Add diluted siRNA to diluted Lipofectamine® RNAiMAX Reagent (1:1 ratio).  Incubate for 5 minutes at room temperature and add to cells.  Incubate cells for 1day at 37°C and later transfect by electroporation with 2 μg of circularized wt HPV18 or wt HPV11 genome and incubate for another 48 h

Manufacturer protocol Publication protocol 1 Relevant paper

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