<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all cases proteins were present at 1 mg/ml. Each chromatogram is labeled in its upper left corner with the protein mixture.</p
<p>The curves represent two SEC purifications runs, on the same column and in similar conditions (se...
Size exclusion chromatography (SEC) is a historical technique widely employed for the detailed chara...
<p>The extent of phosphorylation, which was determined by quantitative densitometry of urea PAGE gel...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>Separate samples were prepared for each time point in SEC buffer. In all cases proteins were pres...
<p>150 μl of sample containing variable quantities of protein (10–120 μg) were loaded on the column ...
<p>Aggregation is shown in gray and aggregation suppression is shown in black, with the suppression ...
<p>Calculated molecular mass is an average of at least three independent experiments. ΔN-HtrA3 to β-...
<p>Size exclusion chromatograms of wild-type Fc and disulfide bond stabilized Fc-mutants monitored a...
Size exclusion chromatography traces of recombinant proteins (1mg/mL) with oligomeric states illustr...
<p>Components within protein A purified supernatant collected at the end of culture were separated b...
Biopharmaceutical drugs are large, complex protein molecules derived from living cells. The characte...
Biopharmaceutical drugs are large, complex protein molecules derived from living cells. The characte...
<p>(<b>A</b>) Crosslinking of mutant p24:V3 chimera. Proteins were separated in non reducing SDS-PAG...
<p>On each panel elution profiles of the isolated wild type HspB1 (blue line), isolated E41K mutant ...
<p>The curves represent two SEC purifications runs, on the same column and in similar conditions (se...
Size exclusion chromatography (SEC) is a historical technique widely employed for the detailed chara...
<p>The extent of phosphorylation, which was determined by quantitative densitometry of urea PAGE gel...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>Separate samples were prepared for each time point in SEC buffer. In all cases proteins were pres...
<p>150 μl of sample containing variable quantities of protein (10–120 μg) were loaded on the column ...
<p>Aggregation is shown in gray and aggregation suppression is shown in black, with the suppression ...
<p>Calculated molecular mass is an average of at least three independent experiments. ΔN-HtrA3 to β-...
<p>Size exclusion chromatograms of wild-type Fc and disulfide bond stabilized Fc-mutants monitored a...
Size exclusion chromatography traces of recombinant proteins (1mg/mL) with oligomeric states illustr...
<p>Components within protein A purified supernatant collected at the end of culture were separated b...
Biopharmaceutical drugs are large, complex protein molecules derived from living cells. The characte...
Biopharmaceutical drugs are large, complex protein molecules derived from living cells. The characte...
<p>(<b>A</b>) Crosslinking of mutant p24:V3 chimera. Proteins were separated in non reducing SDS-PAG...
<p>On each panel elution profiles of the isolated wild type HspB1 (blue line), isolated E41K mutant ...
<p>The curves represent two SEC purifications runs, on the same column and in similar conditions (se...
Size exclusion chromatography (SEC) is a historical technique widely employed for the detailed chara...
<p>The extent of phosphorylation, which was determined by quantitative densitometry of urea PAGE gel...
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