<p>(<b>A</b>) Crosslinking of mutant p24:V3 chimera. Proteins were separated in non reducing SDS-PAGE conditions on a 10% polyacrilamide gel. The p24:V3 CC and CCAA mutants migrate almost exclusively as hexamers, while the p24:V3 WT chimera migrates as monomer. (<b>B</b>) Size exclusion chromatographic profile. Profile of p24:V3 WT (gray) and p24:V3 CCAA mutant (black) on Superdex-200 PC column is shown. Elution volumes of protein standards such as ferritin (440 kDa,dashed and dotted line) and aldolase (158 kDa, dotted line) are also indicated.</p
(A). Analyses of purified WT and mutant sA28 proteins using gel filtration chromatography. Gel-filtr...
<p>Lower panel: Optical density at UV<sup>280</sup> of the effluent of the Superdex 200HR column aft...
<p>αA-WT crystallin and αA-G98R crystallin are preincubated at 37°C, as indicated under methods, and...
<p>(A) Native PAGE analysis of Redβ protein variants. Proteins (10 µg per lane) were separated on a ...
<p>The left lane is the V240C mutant protein and the right lane is the V240C chimera. The mol wt sta...
<p>All gels were loaded in the same manner. Lane 1: Dual color protein ladder (BioRad, Hercules, CA)...
Size exclusion chromatography traces of recombinant proteins (1mg/mL) with oligomeric states illustr...
<p>Arrow denotes expected 58 kDa chimeric protein bands. Lane 1: Dual color protein ladder (BioRad, ...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>All samples were reduced and boiled prior to loading and electrophoresis on a 15% SDS-PAGE gel th...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>A. Size exclusion chromatography elution profile of the UV trace at 280-type CD27L. There are thr...
Fig. 2. Size exclusion chromatography (SEC) profiles of affinity chromatography purified wild-type a...
<p>Panel A shows absorbance at 280 nm as a function of the elution volume, and Panel B is the calibr...
<p>Size exclusion chromatograms of wild-type Fc and disulfide bond stabilized Fc-mutants monitored a...
(A). Analyses of purified WT and mutant sA28 proteins using gel filtration chromatography. Gel-filtr...
<p>Lower panel: Optical density at UV<sup>280</sup> of the effluent of the Superdex 200HR column aft...
<p>αA-WT crystallin and αA-G98R crystallin are preincubated at 37°C, as indicated under methods, and...
<p>(A) Native PAGE analysis of Redβ protein variants. Proteins (10 µg per lane) were separated on a ...
<p>The left lane is the V240C mutant protein and the right lane is the V240C chimera. The mol wt sta...
<p>All gels were loaded in the same manner. Lane 1: Dual color protein ladder (BioRad, Hercules, CA)...
Size exclusion chromatography traces of recombinant proteins (1mg/mL) with oligomeric states illustr...
<p>Arrow denotes expected 58 kDa chimeric protein bands. Lane 1: Dual color protein ladder (BioRad, ...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>All samples were reduced and boiled prior to loading and electrophoresis on a 15% SDS-PAGE gel th...
<p>Separate samples were prepared for each time point in SEC buffer. Times given are in days. In all...
<p>A. Size exclusion chromatography elution profile of the UV trace at 280-type CD27L. There are thr...
Fig. 2. Size exclusion chromatography (SEC) profiles of affinity chromatography purified wild-type a...
<p>Panel A shows absorbance at 280 nm as a function of the elution volume, and Panel B is the calibr...
<p>Size exclusion chromatograms of wild-type Fc and disulfide bond stabilized Fc-mutants monitored a...
(A). Analyses of purified WT and mutant sA28 proteins using gel filtration chromatography. Gel-filtr...
<p>Lower panel: Optical density at UV<sup>280</sup> of the effluent of the Superdex 200HR column aft...
<p>αA-WT crystallin and αA-G98R crystallin are preincubated at 37°C, as indicated under methods, and...