Addition of 3' A overhangs to PCR products

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Revision as of 21:00, 18 October 2008 by S. Mohsen Hosseini (talk | contribs) (Procedure)


Mohsen Hosseini


If PCR is performed using a proofreading DNA polymerase, such as Pfu DNA polymerase, the product will have blunt ends. Taq DNA polymerase catalyzes the non-template directed addition of an adenine residue to the 3´-end of both strands of DNA molecules to make it suitable for TA cloning.



  • Purified PCR product
  • dATP
  • PCR buffer with Mg
  • Taq DNA Polymerase
  • ddH2O


  • Thermocycler or Heat block equilibrated at 72°C
  • Spectrophotometer


1. Purify the PCR product Critical step.png

2. Prepare Taq DNA polymerase reaction mix for a typical 20 - 50 μl reaction:

Final Concentration Volume(μl)
Purified PCR product 0.15 to 1.5 pmol variable
dATP (10 mM) 0.2 mM 1
PCR Buffer with Mg (10x) 1x (1.5 mM MgCl2) 5
Taq DNA Polymerase (5 U/μl) 1U 0.2
ddH2O - up to 50 μl

The A-addition reaction works best when a specific amount of the PCR product is used. The recommended amount is 10–100 ng PCR product for each 100 bp length of the PCR product. This corresponds to 0.15–1.5 pmol PCR product (see table below).

PCR product size Amount of PCR product to use
100 bp 10–100 ng
250 bp 25–250 ng
1000 bp 100–1000 ng

3. Incubate 20 min at 72 °C.

4. Proceed to TA cloning. For optimal ligation efficiency, it's best to use fresh PCR products, since 3´A-overhangs will gradually be lost during storage.

Critical steps




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