<p>1 µl of the lysate and 15 µl of the purified fractions were applied to 16% polyacrylamide gels <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0059820#pone.0059820-Laemmli1" target="_blank">[56]</a>. Lane 1: cell lysate, lane 2: eluate after affinity chromatography via Ni NTA–Agarose, lane 3: eluate after Aβ1-16-GB1-NHS-Sepharose affinity chromatography. Target protein is more than 99% pure after final purification step.</p
<p>(A) HeLa cytoplasmic lysate was applied to m<sup>7</sup>G-sepharose 4B or sepharose 4B alone. Pre...
<p>A/ Purification of <i>NoCKX1</i> expressed from pMAL-c4X vector. Lane 1: molecular mass standard;...
<p>Recombinant fusion proteins were first purified by Ni-chelating affinity chromatography. After th...
Lane M, Molecular Marker (Color Prestained Protein Standard, Broad Range, NEB); lane 1, culture supe...
<p>The progress of purification was monitored by SDS-PAGE (NuPAGE 4–12% Bis-Tris gel, Invitrogen, 1×...
<p>(A) Chromatogram and the SDS-PAGE and the western blot analysis results of the Ni-NTA column chro...
<p>SDS PAGE analysis by Coomassie brilliant blue staining. A.1: protein mixture (cleared cell lysate...
<p>(A) Elution profile of Ni-NTA IMAC chromatography. FGF19 Protein didn’t exist in flow-through (FT...
<p>This figure shows a chromatogram from the purification of JEV NS2B(H)-NS3(pro) by Ni<sup>2+</sup>...
<p>(A) Ni-affinity chromatogram of the βDDM extraction. Blue curve: UV absorbance at 280 nm; green c...
<p>A: Typical fractionation chromatogram of 1 gram IVIG on a 90 mL SNA-agarose column, showing the S...
<p>Proteins were separated by SDS-PAGE and stained using Coomassie Brilliant Blue. Lane 1, pooled fr...
<p>(<b>A</b>) Protein purification by Ni-NTA chromatography of 13 constructs expressed in <i>E. coli...
<p>(A) First run of chromatography for purification (SDS profile shown in <a href="http://www.ploson...
<p><b>A</b>: supernatants 1, 2, 3, 4 obtained from steps 1-4 following expression in BL21(DE3) cells...
<p>(A) HeLa cytoplasmic lysate was applied to m<sup>7</sup>G-sepharose 4B or sepharose 4B alone. Pre...
<p>A/ Purification of <i>NoCKX1</i> expressed from pMAL-c4X vector. Lane 1: molecular mass standard;...
<p>Recombinant fusion proteins were first purified by Ni-chelating affinity chromatography. After th...
Lane M, Molecular Marker (Color Prestained Protein Standard, Broad Range, NEB); lane 1, culture supe...
<p>The progress of purification was monitored by SDS-PAGE (NuPAGE 4–12% Bis-Tris gel, Invitrogen, 1×...
<p>(A) Chromatogram and the SDS-PAGE and the western blot analysis results of the Ni-NTA column chro...
<p>SDS PAGE analysis by Coomassie brilliant blue staining. A.1: protein mixture (cleared cell lysate...
<p>(A) Elution profile of Ni-NTA IMAC chromatography. FGF19 Protein didn’t exist in flow-through (FT...
<p>This figure shows a chromatogram from the purification of JEV NS2B(H)-NS3(pro) by Ni<sup>2+</sup>...
<p>(A) Ni-affinity chromatogram of the βDDM extraction. Blue curve: UV absorbance at 280 nm; green c...
<p>A: Typical fractionation chromatogram of 1 gram IVIG on a 90 mL SNA-agarose column, showing the S...
<p>Proteins were separated by SDS-PAGE and stained using Coomassie Brilliant Blue. Lane 1, pooled fr...
<p>(<b>A</b>) Protein purification by Ni-NTA chromatography of 13 constructs expressed in <i>E. coli...
<p>(A) First run of chromatography for purification (SDS profile shown in <a href="http://www.ploson...
<p><b>A</b>: supernatants 1, 2, 3, 4 obtained from steps 1-4 following expression in BL21(DE3) cells...
<p>(A) HeLa cytoplasmic lysate was applied to m<sup>7</sup>G-sepharose 4B or sepharose 4B alone. Pre...
<p>A/ Purification of <i>NoCKX1</i> expressed from pMAL-c4X vector. Lane 1: molecular mass standard;...
<p>Recombinant fusion proteins were first purified by Ni-chelating affinity chromatography. After th...