10 11
Place microfuge tube on magnetic rack
for 1 min.
Transfer pure plasmid supernatant to a
clean microfuge tube.
9Add 50–200µl of Elution Buer and mix
well by pipetting up-down (10–15x) until
solution is homoegenous.
Incubate for 1 min.
8Repeat with 600µl of Wash Buer #2,
place on magnetic rack for 1 min.
Discard supernatant and leave to dry
for 1–5 mins.
Elution Buer
6Place microfuge tube on magnetic
rack for 1 min. Discard supernatant. 7Add 600µl of Wash Buer #1 and
mix well by pipetting up-down
(5–10x) until solution is homogenous.
Place microfuge tube on magnetic
rack for 1 min. Discard supernatant.
Add 400µl of Binding Buer to the
supernatant in the new microfuge tube
and mix well by pipetting up-down
(10-15x) until solution is homogenous.
Incubate for 1 min at room temp.
5
Place tube on magnetic rack for 1 min.
Transfer supernatant to a new microfuge
tube. Discard previous tube.
4
2Add 200µl of Lysis Buer and mix well by
pipetting up-down (5–10x) until solution is
homogenous.
Incubate for 8 mins at room temp.
Lysis Buer
3Add 100µl of Neutralization Buer and
mix well by pipetting up-down (5–10x).
Incubate for 2 mins at room temp.
Neutralization Buer
Binding Buer
Pellet 1–10ml of bacterial cell sample.
(<5ml for high-copy plasmid, <10ml for
low-copy plasmid). Discard supernatant.
Add 200µl of Resuspension Buer to
the pellet and mix well by pipetting
up-down until solution is homogenous.
1
Resuspension Buer
Wash Buer #1
Wash Buer #2
1.0
Plasmid Miniprep Kit
Plasmid Miniprep Kit
Quick Start Guide