<p>(A and C) The panels showed the sedimentation coefficient distributions <i>c(s)</i> of purified M1N from the 17.6-ml fraction at pH 7.4 (A), and from the 17.4-ml fraction at pH 5.0 (C). The data were acquired at a protein concentration of 1.2 mg/ml. (B and D) The molecular mass distribution derived from <i>c(s)</i> data of panel A and C, respectively.</p
<p>The oligomerization of M1 was analyzed on a Superdex 200 HR 10/30 column. (A) Purified M1 from ni...
Analytical ultracentrifugation (AU) is reemerging as a versatile tool for the study of proteins. Mon...
ABSTRACT We have investigated the potential of sedimentation velocity analytical ultracentrifugation...
Analytical ultracentrifugation (AU) is re-emerging as a versatile tool for the study of proteins. Mo...
<p>Top panels, raw data; absorbance at 280 nm plotted as a function of the radial position, every fi...
AbstractSedimentation velocity analytical ultracentrifugation is an important tool in the characteri...
<p>(A) After affinity chromatography, purified M1C without the N-terminal GST tag (affinity), yielde...
In 1928 Rinde first pointed out the possibility of obtaining molecular weight distributions from sed...
<p>(<b>A</b>) MaviP35-FLAG proteins were purified from bacteria (gray line) and yeast (black line) a...
<p>(A) Sedimentation velocity experiment. Fitted data (upper panel) with residual plots (middle pane...
The partial-specific volume of proteins is an important thermodynamic parameter required for the int...
Molecular weights (molar masses), molecular weight distributions, dissociation constants and other i...
<p>(A) Purified M1N from nickel affinity chromatography yielded five peaks on Superdex 200. The volu...
The partial-specific volume of proteins is an important thermodynamic parameter required for the int...
<p>Superposition of selected sedimentation profiles obtained at 278 nm and the corresponding fitted ...
<p>The oligomerization of M1 was analyzed on a Superdex 200 HR 10/30 column. (A) Purified M1 from ni...
Analytical ultracentrifugation (AU) is reemerging as a versatile tool for the study of proteins. Mon...
ABSTRACT We have investigated the potential of sedimentation velocity analytical ultracentrifugation...
Analytical ultracentrifugation (AU) is re-emerging as a versatile tool for the study of proteins. Mo...
<p>Top panels, raw data; absorbance at 280 nm plotted as a function of the radial position, every fi...
AbstractSedimentation velocity analytical ultracentrifugation is an important tool in the characteri...
<p>(A) After affinity chromatography, purified M1C without the N-terminal GST tag (affinity), yielde...
In 1928 Rinde first pointed out the possibility of obtaining molecular weight distributions from sed...
<p>(<b>A</b>) MaviP35-FLAG proteins were purified from bacteria (gray line) and yeast (black line) a...
<p>(A) Sedimentation velocity experiment. Fitted data (upper panel) with residual plots (middle pane...
The partial-specific volume of proteins is an important thermodynamic parameter required for the int...
Molecular weights (molar masses), molecular weight distributions, dissociation constants and other i...
<p>(A) Purified M1N from nickel affinity chromatography yielded five peaks on Superdex 200. The volu...
The partial-specific volume of proteins is an important thermodynamic parameter required for the int...
<p>Superposition of selected sedimentation profiles obtained at 278 nm and the corresponding fitted ...
<p>The oligomerization of M1 was analyzed on a Superdex 200 HR 10/30 column. (A) Purified M1 from ni...
Analytical ultracentrifugation (AU) is reemerging as a versatile tool for the study of proteins. Mon...
ABSTRACT We have investigated the potential of sedimentation velocity analytical ultracentrifugation...