SAMRSTM
Self Avoiding Molecular Recognition Systems: SAMRSTM
Easy test design. Dozens of targets. Expand/change assays at will.
Problem
To amplify DNA/RNA, large amounts of DNA in large numbers are added to samples as primers and probes. Unfortunately, these large amounts often interact with each other, causing the assay to collapse.

With natural DNA, the need to prevent reactions between primers constrains multiplex assay design and manufacturing even at low levels of multiplexing. With more than ~20 targets, the multiplex loses robustness, and then collapses entirely.
Solution
Modify bases in DNA primers so they bind only to the desired DNA target, not to each other.




Impact
Many assays demonstrate the value of SAMRS
  • Assays with dozens of targets
  • Multiple with speed and sensitivity of a single target
  • Single-tube multiplexed panels streamline workflow
  • Fast, inexpensive multiplex modification for emerging pathogens
  • Wide manufacturing tolerances; less product rejection
Chemistry behind SAMRSTM

SAMRS bases (a, t, g, c) resemble standard bases (A, T, G, C), but strategically omit hydrogen bond units.

SAMRS a pairs with natural T, SAMRS t pairs with natural A, SAMRS g pairs with natural C, and SAMRS c pairs with natural G. However, SAMRS a does not pair with SAMRS t, and SAMRS g does not pair with SAMRS c.