Reaktion #328653

Reaktionsgleichung

triethanolamine

acetic acid

→

triethanolamine acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengena range of triethanolamine acetate concentrations at pH 7.4 in the absence of any salt such as NaCl
2. 2
   WaschenThe bound CA was eluted
3. 3
   Waschena final wash of the column
4. 4
   Sonstigea micro membrane dialysis system

Vorschrift

Polydispersed CA was also fractionated by Sepharose Q FF (1 ml matrix, prepacked) using a range of triethanolamine acetate concentrations at pH 7.4 in the absence of any salt such as NaCl. The triethanolamine acetate buffer was prepared using triethanolamine and adjusting the pH to 7.4 using acetic acid. Polydispersed CA (40 mg; 1 ml) (22.7 kDa; pd 1.34) was loaded on to a Q FF column (1 ml matrix; prepacked). The bound CA was eluted by passing 1 ml of each triethanolamine acetate buffer (300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400 and 1500 mM triethanolamine acetate) through the column at a flow rate of 1 ml/min with a final wash of the column using 200 mM triethanolamine acetate. A small sample of each fraction (20 il) was then buffer exchanged with water using a micro membrane dialysis system, lyophilised and then analysed by native PAGE (20% TBE gel stained with alcian blue).

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