Copyright
©The Author(s) 2005.
World J Gastroenterol. Jul 21, 2005; 11(27): 4180-4187
Published online Jul 21, 2005. doi: 10.3748/wjg.v11.i27.4180
Published online Jul 21, 2005. doi: 10.3748/wjg.v11.i27.4180
Figure 2 SDS-PAGE (150 g/L) analyses of recombinant A2-BSP and β2m proteins expressed in E.
coli strain BL21(DE3). Lane 1: BL21 (pET-β2m) before IPTG induction; lane 2: BL21 (pET-β2m)+IPTG; lane 3: supernatant of BL21 (pET-β2m) lysate; lane 4: washed inclusion body of β2m; lane 5: MW marker; lane 6: BL21 (pET-3c)+IPTG; lane 7: BL21 (pET-A2-BSP) before IPTG induction; lane 8: BL21 (pET-A2-BSP)+IPTG; lane 9: supernatant of BL21 (pET-A2-BSP) lysate; lane 10: washed inclusion body of A2-BSP. HC: heavy chain.
- Citation: He XH, Xu LH, Liu Y. Procedure for preparing peptide-major histocompatibility complex tetramers for direct quantification of antigen-specific cytotoxic T lymphocytes. World J Gastroenterol 2005; 11(27): 4180-4187
- URL: https://www.wjgnet.com/1007-9327/full/v11/i27/4180.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i27.4180