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pUC19 control

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#1 EbolaZaire



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Posted 29 September 2009 - 07:00 AM


I'm doing TOPO TA cloning and think I set up my positive control using the pUC19 plasmid wrong. In the vector ligation reaction I simply replaced PCR product with the pUC19 plasmid; is this correct? Nothing grew on my positive control plate, but colonies grew for my samples and nothing grew for my negative control which leads me to believe I didn't set up the positive control correctly. Help?

#2 bac



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Posted 29 September 2009 - 11:26 AM

if I got your message right, you used pUC19 as insert with a TOPO vector (which one? just out of curiosity).
Then well yes, I think you set the positive control wrong. It would be hard to get ligated a circular plasmid (pUC19) into the TOPO vector, so I would not be surprised that you had no colonies. What about the actual cloning samples?

pUC19 is provided in the kit for two reasons: first to check the transformation efficiency of your competent EColi*. In this case you would have only to transform pUC19 into competent EColi (not to set up the cloning reaction). Then I think you can use it as positive control for M13 PCR if you want then to screen the colonies having the right insert.

* see p 18 in this manual http://tools.invitro.../topota_man.pdf
Note: I provided the link just as reference, it can be that this manual is not of the same kit you are using, there are several TOPO TA kits!

hope this helps

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