Zyppy MiniPrep Protocol
#D4020 from Zymo Research
- For each miniprep, grow 2 ml culture, 37° C, overnight (O/N) in appropriate medium and anitbiotic (usually
ampicillin,but not always); shake at 400 RPM and slant tubes. You can grow as much as 8 mL of overnight culture and repeatedly pellet the cells into a microfuge tube to get more plasmid from each miniprep.
- Add 600 µL of O/N culture to an appropriately
labeled 1.5 mL microfuge tube. Save the rest of the O/N culture
at +4 ° C and keep them sterile.
You can increase your yield by pelleting up to 3 mL of O/N culture and resuspending
pellet very well in 600 µL water or TE.
- Add 100 µL 7X
Lysis Buffer (blue color) .
Mix by inverting the tube 4-10 times.
Solution should become clear instead of opaque.
Proceed to the next step within
- Add 350 µL of Neutralization
Buffer (yellow color; RNase A already added) and
by inverting the tube until the entire solution and precipitate
This buffer is stored at +4 ° C.
- Spin full speed for 2 minutes at RT°.
- Prepare Zymo-Spin II column (with binding
resin) by inserting into 2 mL collection tube. Be sure to label
the spin column and the collection tube. Also label a 1.5 mL microfuge
tube for use in step 14.
- Transfer ~900 µL supernatant
to Zymo-Spin II column. Do not transfer any of the solid
- Spin full speed for 15 seconds at RT°.
liquid flowthrough and reinsert Zymo-Spin II
column into same collection
- Add 200 µL Endo-Wash
Buffer to the Zymo-Spin II column. Repeat this step a second time.
- Spin full speed for 15
seconds at RT°. No need
to empty flow through.
- Add 400 µL Zyppy
Wash Buffer (with
ethonol already added).
Repeat this step a second time.
- Spin full speed for 30 seconds at RT°. Discard
liquid flowthrough and and the 2 mL collection tube. The DNA is still
in the spin column.
- Transfer Zymo-Spin
II column to a clean and appropriately labeled 1.5 mL microfuge
tube (from step 6 above).
- Add 30 µL Zyppy
Elution BUffer ot the center of the to
the Zymo-Spin II column. Let
it stand for 1 minute to maximize yield.
- Spin full speed for 30
seconds at RT°. SAVE
THE LIQUID with your plasmid. Reaload the eluate onto the same column and let it sit for one minute. Spring the column again and recapture the eluate in the same tube. Discard the spin
column. Store DNA at -20° C.
- If you want to digest some DNA, 5-10 µL
of the MP DNA in a final volume of 20 µL is a nice place
to start. You can NanoDrop the DNA if you need to know the
2012 Department of Biology, Davidson College, Davidson, NC 28036
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