16s worked and my plasmid looked good on the gel. Estimating from the ladder my template was around .06 nanograms in the PCR reaction. But Phusion, Phusion + DMSO, Q5, and Q5 + DMSO all failed to amplify.
A friend is sending me some primers that he's used successfully on pVIB before, I'll try it out and see how it goes. He doesn't remember exactly what they amplify but maybe I can figure it out and use them to figure out what's going on with my reaction.
--
-- You received this message because you are subscribed to the Google Groups DIYbio group. To post to this group, send email to diybio@googlegroups.com. To unsubscribe from this group, send email to diybio+unsubscribe@googlegroups.com. For more options, visit this group at https://groups.google.com/d/forum/diybio?hl=en
Learn more at www.diybio.org
---
You received this message because you are subscribed to the Google Groups "DIYbio" group.
To unsubscribe from this group and stop receiving emails from it, send an email to diybio+unsubscribe@googlegroups.com.
To post to this group, send email to diybio@googlegroups.com.
Visit this group at https://groups.google.com/group/diybio.
To view this discussion on the web visit https://groups.google.com/d/msgid/diybio/4b4796a0-f9e9-4990-b470-b762b3a22947%40googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
[DIYbio] Re: PCR trouble
6:48 AM |
Subscribe to:
Post Comments (Atom)






0 comments:
Post a Comment