Sauer:GFP-H6-ssrA purification: Difference between revisions
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Expression | Expression | ||
Grow cells at | Grow cells at 30°C. | ||
Innoculate 1L of LB or TB + Amp with 10mL of overnight culture. | Innoculate 1L of LB or TB + Amp with 10mL of overnight culture. | ||
Induce cells with 0.5mM IPTG at OD ~0.7 | Induce cells with 0.5mM IPTG at OD ~0.7 | ||
After ~ 3 hrs harvest cells by centrifugation, 20m x 4krpm | After ~ 3 hrs harvest cells by centrifugation, 20m x 4krpm | ||
Freeze cells (- | Freeze cells (-80°C) with 5mL H6 protein lysis buffer. | ||
Purification | Purification | ||
| Line 16: | Line 16: | ||
Ni-NTA column | Ni-NTA column | ||
pre-incubate supernatant with washed Ni-NTA slurry. (~30m with shaking in cold room) | pre-incubate supernatant with washed Ni<sup>2+</sup>-NTA slurry. (~30m with shaking in cold room) | ||
Wash with ~50mL NB | Wash with ~50mL NB | ||
Revision as of 08:28, 18 June 2008
Expression
Grow cells at 30°C. Innoculate 1L of LB or TB + Amp with 10mL of overnight culture. Induce cells with 0.5mM IPTG at OD ~0.7 After ~ 3 hrs harvest cells by centrifugation, 20m x 4krpm Freeze cells (-80°C) with 5mL H6 protein lysis buffer.
Purification Thaw with additional 5mL lysis buffer and protease inhibitor (Roche EDTA free protease inhibitor capsules work well)
Lyse by your favorite method
Centrifuge- 30m x 15krpm
Ni-NTA column pre-incubate supernatant with washed Ni2+-NTA slurry. (~30m with shaking in cold room)
Wash with ~50mL NB
Elute with ~10mL NE, take 1mL fractions.
Concentrate as needed.
For all buffers see Sauer:Purification_of_His-tagged_proteins/Native_prep
