<p>Lanes M, protein standards; 1, before induction with 1 mM IPTG; 2, after cells were induced with IPTG and grown at 37°C for 5 h; 3, recombinant protein purified under native conditions with the ProBond™ purification system. Arrows designate the positions of the proteins on the gels.</p
<p><i>E</i>. <i>coli</i> BL21 DE3 was transformed with (A) pET43.1-Ppt2 (76 kDa), (B) pET30-Acp1 (16...
RecBCD was purified from E. coli JM109 co-transformed with plasmids pPB800 and pPB520, which were a ...
<p>GST and GST-ST1, -ST2 and -ST3 fusions proteins were expressed in <i>E.coli</i>, extracted, and r...
<p>Lanes: 1, protein molecular weight standard; 2, crude extract of un-induced cells; 3, crude extra...
<p>Lane M, protein molecular marker; Lane 1, before induction with 0.7 mM IPTG; Lane 2, after induct...
<p>The purity of the proteins was analysed by SDS-PAGE using 10% (w/v) gel showing <b>(A)</b> PL1A (...
<p>After induction with IPTG for 12 h, <i>E. coli</i> cells were harvested, total cell contents (W) ...
<p>Lane M: protein marker; Lane 1: total soluble cell lysate; Lane 2: flow-through elution; Lane 3: ...
<p>Each fusion protein was expressed in <i>E. coli</i> and analyzed by SDS-PAGE followed by Coomassi...
<p>(A) Total protein extracts from <i>E. coli</i> cells harbouring either pGEX-3X-NotI-FPS1 or pGEX-...
<p>(A) The protein was induced with IPTG (0.5 mM) at 22°C for 16 h in E. coli BL21(DE3) cells, and a...
<p>A. Left panel, silver-stained gel showing the recombinant proteins with their expected molecular ...
<p>(A) 10% SDS-PAGE analysis of the recombinant proteins from the culture medium (Med), periplasmic ...
<p>Endo-CC1 and Endo-CC2, expressed in <i>E</i>. <i>coli</i>, were purified and then 1 μg of these p...
Protein expression and purification have traditionally been time-consuming, case-specific endeavors,...
<p><i>E</i>. <i>coli</i> BL21 DE3 was transformed with (A) pET43.1-Ppt2 (76 kDa), (B) pET30-Acp1 (16...
RecBCD was purified from E. coli JM109 co-transformed with plasmids pPB800 and pPB520, which were a ...
<p>GST and GST-ST1, -ST2 and -ST3 fusions proteins were expressed in <i>E.coli</i>, extracted, and r...
<p>Lanes: 1, protein molecular weight standard; 2, crude extract of un-induced cells; 3, crude extra...
<p>Lane M, protein molecular marker; Lane 1, before induction with 0.7 mM IPTG; Lane 2, after induct...
<p>The purity of the proteins was analysed by SDS-PAGE using 10% (w/v) gel showing <b>(A)</b> PL1A (...
<p>After induction with IPTG for 12 h, <i>E. coli</i> cells were harvested, total cell contents (W) ...
<p>Lane M: protein marker; Lane 1: total soluble cell lysate; Lane 2: flow-through elution; Lane 3: ...
<p>Each fusion protein was expressed in <i>E. coli</i> and analyzed by SDS-PAGE followed by Coomassi...
<p>(A) Total protein extracts from <i>E. coli</i> cells harbouring either pGEX-3X-NotI-FPS1 or pGEX-...
<p>(A) The protein was induced with IPTG (0.5 mM) at 22°C for 16 h in E. coli BL21(DE3) cells, and a...
<p>A. Left panel, silver-stained gel showing the recombinant proteins with their expected molecular ...
<p>(A) 10% SDS-PAGE analysis of the recombinant proteins from the culture medium (Med), periplasmic ...
<p>Endo-CC1 and Endo-CC2, expressed in <i>E</i>. <i>coli</i>, were purified and then 1 μg of these p...
Protein expression and purification have traditionally been time-consuming, case-specific endeavors,...
<p><i>E</i>. <i>coli</i> BL21 DE3 was transformed with (A) pET43.1-Ppt2 (76 kDa), (B) pET30-Acp1 (16...
RecBCD was purified from E. coli JM109 co-transformed with plasmids pPB800 and pPB520, which were a ...
<p>GST and GST-ST1, -ST2 and -ST3 fusions proteins were expressed in <i>E.coli</i>, extracted, and r...