![]() |
|
![]() |
||||
Thread | Thread Starter | Forum | Replies | Last Post |
How do i get rid of Formamide from my dsDNA? | mzahir89 | Sample Prep / Library Generation | 5 | 10-08-2015 04:05 AM |
QuantiFluor dsDNA Dye System | GSviral | 454 Pyrosequencing | 0 | 12-17-2014 06:50 AM |
Circle graphs | JohnK | Bioinformatics | 2 | 01-28-2011 06:50 AM |
PubMed: Massively parallel display of genomic DNA fragments by rolling-circle amplifi | Newsbot! | Literature Watch | 0 | 07-07-2010 11:20 AM |
![]() |
|
Thread Tools |
![]() |
#1 |
Member
Location: Stillwater Join Date: Dec 2009
Posts: 62
|
![]()
Does anyone have experience with samples using rolling circle amplification that can tell me whether they have relatively high or low amounts of ssDNA? The client is not local so it would help to know in advance whether they need to ship much more based on A260 readings before starting library preps.
Thanks, -p |
![]() |
![]() |
![]() |
#2 |
Senior Member
Location: Oklahoma Join Date: Sep 2009
Posts: 411
|
![]()
Comparing A260 vs picogreen/Qubit should tell you if there's a large amount of ssDNA present.
|
![]() |
![]() |
![]() |
Tags |
rca, rolling circle |
Thread Tools | |
|
|