![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
Truseq RNA kit for making DNA library | elisadouzi | Sample Prep / Library Generation | 3 | 07-17-2013 08:32 AM |
question on DNA fragment size after shear the DNA (in Chip-seq) | kaixinsjtu | Sample Prep / Library Generation | 4 | 04-05-2012 04:36 AM |
Number of PCR How many PCR cycles to enrich adapter-modified DNA fragments | MGH Man | Sample Prep / Library Generation | 5 | 07-26-2010 06:15 AM |
question on making libraries from pcr products | seqgirl123 | Sample Prep / Library Generation | 3 | 02-07-2010 08:55 AM |
emulsion pcr - one template-fragment per bead? | Triticum | 454 Pyrosequencing | 1 | 11-30-2009 11:31 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Junior Member
Location: Japan Join Date: Feb 2011
Posts: 1
|
![]()
Hi all,
I am going to make ligation library from PCR fragments. Roche recommend to use 0.5 microgram of DNA (10^11 molecules as 500 bp) for this and after purification it becomes around 10^9 ends of DNA fragment. It might mean Tags are ligated only to a few % of ends, and thus only 1/10^4 molecules have Tag at both ends. In the protocol, 10^9 ends looks like to mean 10^9 fragments having Tags at both ands and thus can be used for emPCR. So, I must be missing some point, but what is that? ![]() |
![]() |
![]() |
![]() |
Thread Tools | |
|
|