Fig. 2From: Development and evaluation of enzyme-linked immunosorbent assay of nucleic acid sequence-based amplification for diagnosis of invasive aspergillosisDetection of DIG-labeled NASBA products by the microplate hybridization system. NASBA was performed in the presence of 105 CFU Aspergillus spores and then NASBA product was twofold serially diluted before DIG-detection ELISA system (filled square). Negative control consists of NASBA reaction performed in the absence of Aspergillus (open square). Results are averages of triplication analysisBack to article page