11-0027-48 AC, 2007-09 • p12
IMAC purification - any metal
1
Preparing the buffers
•
Use high purity water and chemicals.
•
Filter all buffers through a 0.45 µm filter before use.
Binding buffer (port A1):
20 mM sodium phosphate, 0.5 M NaCl, 20 mM imidazole,
pH 7.4 *
Wash eluent (port A2):
Distilled water
Metal-loading eluent (port A3):
100 mM metal salt solution (metal chloride or metal
sulphate e.g. 100 mM CuSO
4
, 100 mM CoCl
2
or
100 mM ZnCl
2
in distilled H
2
O)
Elution buffer (port B):
20 mM sodium phosphate, 0.5 M NaCl, 0.5 M imidazole,
pH 7.4
Prepare at least 500 ml of each eluent.
*
Alternative buffers:
5–40 mM imidazole can be included in the binding buffer to
reduce unspecific binding of non-histidine-tagged proteins.
The concentration of imidazole is protein dependent and if the
protein of interest elutes or does not bind at a certain imidazole
concentration, then reduce the concentration.
2
Preparing the sample
a) Adjust the sample to composition of binding buffer by:
•
diluting the sample in binding buffer
or
•
by buffer exchange using HiTrap Desalting or HiPrep
26/10 Desalting.
b) Pass the sample through a 0.45 µm filter.
3
Preparing the system
a) Place each inlet tubing from port A (8-port valve) in
eluents as given above and the tubing from port B
(2-port valve) in the elution buffer.
b) Place the three brown waste tubings in waste.
c) Connect the column between port 1 on the injection
valve (7-port valve) and the UV flow cell (see Ordering
information on next page for suitable columns).
d) Fill the fraction collector rack with 18 mm tubes
(minimum 40) and position the white plate on the
fractionation arm against the first tube.
e) Connect a sample loop large enough for your sample
between port 2 and 6 on the injection valve. Use a
syringe to manually fill the loop.
Note: If a Superloop is needed, additional information
is supplied in the instructions for Superloop.
4
Selecting Application Template and
starting the method
a) Check the communication to PrimeView. At the lower
right corner of the screen the text
Controlled By:
prime
should be displayed.
b) Use the arrow and OK buttons to move in the menu
tree until you find
IMAC Purification Uncharged
HiTrap
.
c) Enter the sample volume and press
OK
to start the
template.
Note: If a 5 ml column is preferred, see cue card on
p.36.
Theoretical gradient in
IMAC Purification Uncharged HiTrap
Application Template.
IMAC Purification
Uncharged HiTrap
Set Sample Inj. Vol
(00.0 ml)
00.0
Run Application Template
Press OK to start
Run data displayed
Application Template
Templates
6 1 6
10
20
20
17
5
Min
100
50
Sample
Priming &
water wash
Wash
Elution
Total separation time = 87 min + sample application time
Buffer wash
%B
Re-equili-
bration
Metal-loading
Equilibration
Priming &
water wash
Содержание AKTAprime plus
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