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L line BCM1, the expression of both genes is opposite: no levels of MAGE-A1 [2^(Ct) 1.07] and high levelsof BORIS [2^(Ct) 24.39]. We transiently transfected expression plasmid encoding BORIS into both cell lines, with negligible transcript levels of MAGE-A1, and quantified endogenous MAGE-A1 mRNA by RT (reverse transcription)-PCR and gel electrophoresis. As depicted in Figure 1, BORIS was able to

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L line BCM1, the expression of both genes is opposite: no levels of MAGE-A1 [2^(Ct) 1.07] and high levelsof BORIS [2^(Ct) 24.39]. We transiently transfected expression plasmid encoding BORIS into both cell lines, with negligible transcript levels of MAGE-A1, and quantified endogenous MAGE-A1 mRNA by RT (reverse transcription)-PCR and gel electrophoresis. As depicted in Figure 1, BORIS was able to

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Aline (PBS), and diluted (final, concentration 5 107 CFU/ml) in PBS. Next, 200- l bacterial suspensions were mixed with 200 l of plasma or buffer, followed by incubation for 3 h in human plasma. After three further washing steps with PBS, the pellet was suspended in Tris-NaCl buffer (19.2 mM/1.062 M; pH 7.5) containing 20 g/ml of the chromogenic substrate S-2251 (H-D-Val-Leu-Lys-pNA?HCl; Sigma), f