Boston University/Custom Cloning Protocol


Cloning a chromosomal gene into a plasmid

Whole-Cell PCR (3 hours) -prepare agarose gel Gel electrophoresis with SYBR safe (1 hour) -prepare Qiagen PCR Cleanup Kit Qiagen PCR Cleanup (0.5 hour) -prepare digestion plasmid Prepare digestion of PCR products (0.5 hour) Digestion of PCR products and plasmid (3 hours) -prepare Qiagen PCR Cleanup Kit -prepare agarose gel (SYBR safe) Qiagen PCR Cleanup of PCR products and run gel electrophoresis of plasmid (1 hour) -prepare Qiagen Gel Extraction Kit Qiagen Gel Extraction of plasmid from gel (0.5 hour) -prepare ligation Ligation (1 hour) -prepare competent cells from O/N culture Transformation (0.5 hour) -warm plates Plate cells

Whole-Cell PCR:

1) Pellet 75µl of O/N E.coli K12 culture in an eppy tube

2) Carefully aspirate all supernatant media

3) Put the eppy tube with the pelleted cell on ice

4) Mix the 25 µl PCR cocktail:

The contents of the plates are as follows(column indicates transformation type):
Control 1'(ul)Control 2(ul)PCR(ul)
Primer 12-2
Primer 2-22
Master Mix12.512.512.5

5)Thermocycler 94ºC 5 min 94ºC 30 sec <------ 55ºC 1 min | repeat 35 X 65ºC 4 min <------ 65ºC 10 min

6) Prepare Gel electrophoresis analysis and PCR product cleanup

Gel electrophoresis analysis and PCR product cleanup:

Note that these two steps should be done at the same time by different people

1) Run 5µl of PCR product in a 1.5% agarose gel

50 ml TAE

750 mg agarose

0.5 µl 1% EtBr

120V for 45 minutes

2) Clean up rest of PCR product with a Qiagen PCR cleanup kit

PCR Purification

3) Elute with 35 µl EB instead of 50 µl

4) Measure concentration with the Nanodrop

Plasmid miniprep:

1) Miniprep using a Qiagen Miniprep Kit:

DNA Purification

Note that PCR product and vector digestion can be run simultaneously

PCR product digestion: 1) Prepare 20 µl digestion reaction: 2 µl EcoRI buffer 2 µl BSA 15 µl DNA 0.5 µl EcoRI 0.5 µl HindIII 2) Run digestion for 90 minutes at 37ºC

Clean up: 1) Qiagen PCR cleanup kit (see page 3 for protocol) and elute with 35 µl instead of 50 µl

Plasmid digestion: 1) Use miniprepped plasmid 2) Prepare plasmid digestion reaction

Control 1(ul)Control 2(ul)Double Digestion(ul)
EcoRI Buffer1222

3) Run digestion for 90 minutes at 37 ºC

Plasmid Gel Extraction:

  1. Prepare a 60ml 1% agarose gel with SYBR Safe (or Gold) as a stainer
  2. Run the entire plasmid digestion product on the gel at 120V for 70 minutes
  3. Use the orange transilluminator to visualize
  4. With a scalpel or razor blade, cut a thin slice of gel containing the double-digested DNA band
  5. Put the slice into a microcentrifuge tube
  6. Use the Qiagen Gel Extraction Kit to clean the DNA (Do not use the second QG wash and elute with 35 µl)
BU Gel Extraction 1.jpg
BU Gel Extraction 2.jpg


Ligase Buffer22