Copyright
©The Author(s) 2005.
World J Gastroenterol. Jul 28, 2005; 11(28): 4390-4395
Published online Jul 28, 2005. doi: 10.3748/wjg.v11.i28.4390
Published online Jul 28, 2005. doi: 10.3748/wjg.v11.i28.4390
Figure 2 (PDF) Sensitivity of semi-nested RT-PCR for SARS-CoV.
M: DNA marker (pUC19 DNA/MSP I marker); lane A-G: virus concentration was 106-1010 TCID50, lane H: negative control.
Figure 1 (PDF) Amplification of SARS-CoV RNA BJ-01 by semi-nested RT-PCR.
M: DNA marker (pUC19 DNA/MSP I marker); lane A: 348 bp; lane B: 368 bp; lane C: positive RT-PCR control, 462 bp; lane N: negative RT-PCR control.
Figure 3 (PDF) Amplification of SARS-CoV RNA from stool samples.
M: DNA marker (pUC19 DNA/MSP I marker); lanes 1-11: samples from different SARS patients; N: negative control; P was the positive RT-PCR control from the RNA of SARS-CoV BJ-01.
- Citation: Wang XW, Li JS, Guo TK, Zhen B, Kong QX, Yi B, Li Z, Song N, Jin M, Wu XM, Xiao WJ, Zhu XM, Gu CQ, Yin J, Wei W, Yao W, Liu C, Li JF, Ou GR, Wang MN, Fang TY, Wang GJ, Qiu YH, Wu HH, Chao FH, Li JW. Excretion and detection of SARS coronavirus and its nucleic acid from digestive system. World J Gastroenterol 2005; 11(28): 4390-4395
- URL: https://www.wjgnet.com/1007-9327/full/v11/i28/4390.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i28.4390