• LAMP technology can be
applied in various fields
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 RNA amplification requires only the addition of a
sample to a tube containing a mixture of primers, buffer and a mixture
of Bst DNA polymerase and reverse transcriptase. The reaction is
then incubated at a constant temperature of 60 to 65°C, and is usually
completed within one hour. There is no separate
reverse-transcription step for RNA samples.
• Methods of detection
LAMP amplification results
can be monitored in real time using the cost effective Loopamp®
Realtime Turbidimeter. 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
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