Any ideas why my PCR amplification won't work?
I'm trying to amplify a ~200bp segment from a ~4kb plasmid. A postdoc in my lab previously amplified the segment and gave me a stock of gel-extracted PCR product, the starting plasmid, the primers, and the thermocycle he used (standard 95/5min - [95/30s-55/30s-72/30s]x25cycles - 72/10min).
The template plasmid he gave me is pCDFDuet-1 and the primers are
I'm using NEB Q5® High-Fidelity 2X Master Mix, I just thawed a brand new tube of master mix, mixed well, and keep it on ice/frozen.
I copied his reaction exactly (as far as I can tell) and got no band. I've tried reducing annealing temp, reducing primer conc, reducing template conc, with no luck. The problem is probably not those things though, I think it's the template.
I tried amplifying the segment not just from the stock of Duet plasmid he gave me, but from another plasmid he gave me, DHFR-Duet. He cloned DHFR into Duet himself. When I used that as a template, I got a super strong product band at ~560bp, which is the length of DHFR... In the same test, I made a reaction that was identical except with a different Duet vector test tube (empty plasmid -- no DHFR). That reaction gave no band as well.
0. GeneRuler 100 bp Plus DNA Ladder 100 to 3000
1. Alternate empty Duet
4. Original empty Duet
5. PCR amplicon as template
You can see the gel at:
The postdoc is very organized and this lab runs a tight ship, so it's unlikely he gave me the wrong template. Why am I getting a 500bp product from Duet-DHFR and no product from empty Duet? I should be getting a shorter product from empty Duet at least, if the primers are located on Duet. I tried blasting both primers and only one matches to Duet. Any clues on where these primers match to on either Duet or DHFR? Or other reasons it won't freakin amplify from the template he gave me?
This is my first week as the new grad student in this lab and I really want to make this reaction work...!
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