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1D and 2D Protein Electrophoresis - Institut de Cancérologie et d ...

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Buffer system for 16-BAC acidic<br />

PAGE<br />

Separating gel:<br />

7.5–15% T acrylami<strong>de</strong> (3.25 %C),<br />

0.4 M M<strong>et</strong>hoxy ac<strong>et</strong>ic acid/KOH pH 3.0,<br />

0.002% 16-BAC,<br />

Catalyst system: 4 mM ascorbic acid, 8 µM FeSO 4·7H 2O,<br />

Start of polymerization: add 2.0 mM H 2 O 2 .<br />

Stacking gel:<br />

4%T acrylami<strong>de</strong> (7.8%C),<br />

0.4 M Ac<strong>et</strong>ic acid/KOH pH 4.0,<br />

0.002% 16-BAC,<br />

Catalyst system: 4 mM ascorbic acid, 8 µM FeSO 4 ·7H 2 O,<br />

Start of polymerization: add 2.0 mM H 2 O 2 .<br />

Kramer ML.<br />

A new multiphasic buffer system for benzyldim<strong>et</strong>hyl-n-hexa<strong>de</strong>cylammonium chlori<strong>de</strong><br />

polyacrylami<strong>de</strong> gel electrophoresis of proteins providing efficient stacking.<br />

<strong>Electrophoresis</strong> 27 (2006) 347–356.

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