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. 2013 Mar;20(3):350–357. doi: 10.1128/CVI.00630-12

Fig 1.

Fig 1

Schematic representation of iPCR assay for detection of Lyme disease biomarkers. Intact spirochete (A) or recombinant protein antigen coupled to magnetic beads (B) was used to capture B. burgdorferi-specific host-generated antibodies. A biotinylated DNA oligonucleotide reporter molecule coupled to a streptavidin-conjugated reporter antibody was amplified by qPCR for detection and quantification. (C) Anti-B. burgdorferi antibody coupled to magnetic beads was used for spirochete capture, with detection accomplished by qPCR amplification of the DNA oligonucleotide-coupled reporter antibody, similar to detection of host antibody.