Isothermal amplification is a method that enables nucleic acid detection at a fixed temperature, with this feature making isothermal amplification desirable for use in rapid, portable, point-of-care (POC) assays.
There are several different isothermal amplification methods which utilize different enzymes and master mix components for different applications. For example, Loop-mediated isothermal amplification (LAMP) requires Bst polymerase and works at 65 °C to increase specificity; whereas, Whole Genome Amplification (WGA) requires Phi29 Polymerase and works at lower temperatures (30±5°C). All isothermal amplification methods require DNA polymerases with high strand displacement activity, sequence specific primers for specificity to the target gene, single stranded binding proteins, and secondary enzymes.
At Fortis, we develop and manufacture custom enzymes, proteins, and master mixes that meet all your needs for isothermal amplification assay development - whether it be for detecting RNA or DNA from human, animal or environmental samples on a lateral flow strip or using another detection method.
We have the expertise to custom design isothermal amplification enzymes for common methods, such as LAMP and Whole Genome Amplification (WGA).
Loop-mediated isothermal amplification is a method utilizing a single-tube technique at a constant temperature (around 60-65℃) where 4-6 primers and strand displacing enzymes are used to form a loop structure which enables quick amplification of target genes.
Whole Genome Amplification is another isothermal method that is used to produce large quantities of an entire genome of an organism from a limited amount of starting material.
Isothermal Amplification Enzymes and Mixes | ||
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BST 2.0 ISOMix with EvaGreen Dye | OEM | Contact sales |
BST Prime DNA Polymerase (Strand-displacing) | OEM | Contact sales |