A free web-based primer designing tool is available here.  By designing your own primers, you can apply the LAMP technology in any field, targeting any DNA or RNA template.  To see a list of literature regarding LAMP applications, click here.

• Simple and rapid amplification

The LAMP DNA amplification requires only the addition of a sample to a tube containing a mixture of primers, buffer and Bst DNA polymerase.  The reaction is then incubated at a constant temperature of 60 to 65°C, and is usually completed within one hour. 

•Methods of Detection

The LAMP amplification results can be monitored in real-time using the cost-effective Loopamp® Realtime Turbidimeters.  Alternatively, the endpoint results can be visualized by adding Loopamp® Fluorescent Detection Reagent (sold separately) to the initial master mix.

• For more detailed information, view the Package Insert