using the QIAprep Spin Miniprep Kit and a Microcentrifuge
Resuspend pelleted bacterial cells in 250 ul Buffer P1 and transfer to a microcentrifuge tube.
Ensure that RNase A has been added to Buffer P1. No cell clumps should be visible after resuspension of the pellet.
If LyseBlue reagent has been added to Buffer P1, vigorously shake the buffer bottle to ensure LyseBlue particles are
completely dissolved. The bacteria should be resuspended completely by vortexing or pipetting up and down until no cell clumps remain.
Add 250 ul Buffer P2 and mix thorougly by inverting the tube 4-6 times.
Mix gently by inverting the tube. Do not vortex, as this will result in shearing of genomic DNA. If necessary, continue inverting the tube
until the solution becomes viscous an slightly clear. Do not allow the lysis reaction to proceed for more than 5 min.
If LyseBlue has been added to Buffer P1 the cell suspension will turn blue after addition of Buffer P2. Mixing should
result in a homogeneously colored suspension.
If the suspension contains localized colorless regions of if brownish cell clumps are still visible, continue mixing
the solution until a homogeneously colored suspension is achieved.
Add 350 ul Buffer N3 and mix immediately and thoroughly by inverting the tube 4-6 times.
To avoid localized precipitation, mix the solution thoroughly, immediately after addition of Buffer N3. Large culture
volumes (e.g. > 5 ml) may require inverting up to 10 times. The solution should become cloudy.
If LyseBLue reagent has been used, the suspension should be mixed until all trace of blue has gone and the suspension
is colorless. A homogeneous colorless suspension incated that the SDS has been effectively precipitated.
Centrifuge for 10 min at 13,000 rpm (~17,900 x g) in a table-top microcentrifuge.
A compact white pellet will form
Apply 800 ul pf the supernatant from step 4 to the QIAprep 2.0 spin column by pipetting.
Centrifuge for 30-60 s. Discard the flow-through.
Recommended: Wash the QIAprep 2.0 spin column by adding 0,5 ml Buffer PB and centrifuging for 30-60 s. Discard the flow-through.
This step is necessary to remove trace nuclease activity when using endA+ strains such as the JM series, HB101 and its derivatives,
or any wild-type strain, which have high levels of nuclease activity or high carbohydrate content. Host strains such as XL-1 Blue and DH5a
do not require this additional wash step.
Wash QIAprep 2.0 spin column by adding 0,75 ml Buffer PE and centrifuging for 30-60 sec.
Discard the flow-through, and centrifuge at full speed for additional 1 min to remove residual wash buffer.
important: Residual wash buffer will not be completely removed unless the flow-through is discarded before
this additional centrifugation. Residual ethanol from Buffer PE max inhibit subsequent enzymatic reactions.
Place the QIAprep 2.0 column in a clean 1,5 ml microcentrifuge tube to elute DNA, add 50 ul Buffer EB (10mM Tris-Cl, pH 8.5)
or water to the center of each QIAprep 2.0 spin column, let stand for 1 min, and centrifuge for 1 min.
