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#1 Re: rf-cloning troubles » 2nd PCR not working » 2014-08-15 09:39:50

Hi Steve thank you for the reply. I repeated the 2nd PCR with both the original protocol and with the increased annealing/extension time but only using 1 & 2 ul of the PCR mix after digestion and it all worked perfectly smile The higher annealing temp gave me more colonies so you were right about the dimers. I really appreciate you guiding me through this and definitely know better for any future RF experiments.

Thanks again!

#2 Re: rf-cloning troubles » 2nd PCR not working » 2014-08-13 08:05:01

Yep had another look in the project management section and it's there thanks smile

I didn't have a positive control in the last transformations I tried for RF but I used the cells from the same batch for a regular Maxi prep and they worked fine and the transformation protocol hasn't changed. I should probably include a control in subsequent transformations just to rule it out.

I used the entire PCR reaction to transform. Was that correct? I assumed that as it is a rare event it would be better to use all of it...

There was absolutely nothing on either plates and I know I've got the right antibiotic.

#3 Re: rf-cloning troubles » 2nd PCR not working » 2014-08-12 17:21:30

Thanks for the quick reply. I tried to find the project on plasmid management after going through the rf-cloning.org home page but couldn't see it. The construct name was pEF1-mNeptune.

I transformed the DpnI digested PCR into OneShot MAX efficiency DH5a chemically competent cells from Life Tech. using the standard 42 degrees heat shock protocol. Shook them for half an hour in SOC at 37 then plated the whole volume onto two LB+Amp plates

#4 rf-cloning troubles » 2nd PCR not working » 2014-08-12 16:51:07

ZacJ
Replies: 8

Hi there,

I really like the RF cloning protocol and have been trying to swap the V5/His tag in the pEF1 vector with an mNeptune sequence. My first PCR works really well and I get good yield from the gel extraction but when I try the 2nd PCR I get no colonies at the end. The 2nd PCR product is treated with DpnI which must work as I don't get any false positives. I have tried both the 2-step and the 3-step with 60 degrees annealing temperature but to no avail. The only thing that I can think of is something to do with the plasmid annealing part of the megaprimer. I'm not sure whether the details provided by the website are on record somewhere...

I hope you can help.

BW,
Zac

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