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Volume 10, Number 7, July 2004 SARS Coronavirus DetectionAndreas Nitsche,* Brunhilde Schweiger,* Heinz Ellerbrok,* Matthias
Niedrig,* and Georg Pauli* |
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Figure. LightCycler amplification curves of the three single SARS-coronavirus (CoV)-specific assays and the combined assay. Five hundred genome equivalents (GE) of SARS-CoV were amplified with the three single assays-NS pp1a, NS pp1ab, and SS GP-as well as with the combination of the three assays. No fluorescence signal was observed for control pathogens. In the inset, the respective agarose gel analysis of the amplification products in a 3% gel is shown. Lane 1: 50-bp marker, lane 2: 500 GE SARS-CoV amplified with the assay combination (products of assays NS pp1ab and SS GP are not clearly distinguishable because of sizes of 88 bp and 79 bp, respectively), lane 3: human CoV 229E, lane 4: respiratory syncytial virus, lane 5: rhinovirus, lane 6: human metapneumovirus, lane 7: Mycoplasma pneumoniae, or lane 8: Chlamydia pneumoniae. |
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This page last reviewed June 8, 2004 |
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Emerging
Infectious Diseases Journal |
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