Ambient-temperature Stable LAMP Master Mixes

Superior Sensitivity with Shorter Time-to-Results (TTR)

A) Air-Dryable™ DNA LAMP (MDX119)

B) Air-Dryable™ RNA/DNA LAMP (MDX118)

50

80

40

60

30

40

20

20

10

0

0

20 copies/rxn

NTC

500 copies/rxn 100 copies/rxn 10 copies/rxn

1000 copies/rxn 100 copies/rxn

1000 copies/rxn

(A) Conserved regions from the S and P genes of Hepatitis B Virus (1,000, 100 and 20 copies respectively) were amplified using Air-Dryable™ DNA LAMP (MDX119) in an air-dried ( red ) or liquid ( blue ) format or using NEB WarmStart® ( orange ). (B) Emesvirus (MS2) was amplified using Air- Dryable™ RNA/DNA LAMP (MDX118) in an air-dried ( red ) or liquid ( blue ) format or using NEB WarmStart® ( orange ). Reactions were incubated at 65°C for 60 min and TTR were measured at 1:10 of end fluorescence. Error bars represent standard deviation over 4 technical replicates. At lower copy numbers, NEB WarmStart® (orange) exhibited significantly lower reaction reproducibility compared to Air-Dryable™ DNA LAMP Mix, and a lower TTR was observed for reactions using both Air-Dryable™ DNA LAMP Mix and Air-Dryable™ DNA/RNA LAMP Mix across all dilutions of the Hepatitis B gene and MS2-RNA respectively. The results therefore demonstrate greater sensitivity of Air-Dryable™ LAMP Mixes with shorter TTR across all template concentrations.

High Reaction Specificity with Little-To-No Non-Specific Amplification

Air-Dryable™ RNA/DNA LAMP (MDX118)

EBV-DNAM

S2-RNA

Air-Dryable™ RNA/DNA LAMP (MDX118, blue ) was compared to NEB WarmStart® (orange) for detection of EBV DNA (1,000 ipc) and MS2 RNA (1,000 ipc). Reactions were incubated at 65°C for 60 min and TTR were measured at 1:10 of end fluorescence. Amplification plots of 3 technical replicates demonstrate Air- Dryable™ RNA/DNA LAMP mix has earlier TTR and no non-specific amplification compared to NEB WarmStart® which has detectable amplification for non-template controls (NTC).

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