Table 2.
Method | Advantages | Drawbacks |
Chemical or enzymatic synthesis | Rapid Enzymatic: no need to test individual siRNA Chemical: high purity |
Transient RNAi Needs transfection Enzymatic: variable purity & specificity Chemical: expensive |
DNA plasmid vector or casette | Less expensive Stable RNAi |
Labor intensive Needs transfection |
Viral vector | Stable RNAi May be effective in cells resistant to transfection with dsRNA/plasmids |
Labor intensive Potential biohazard |