| | |||||||
| Register | Search | Today's Posts | Mark Forums Read |
| Protocols and Methods Forum Post Any Protocol, Method, Technique, Procedure or Tips / Troubleshooting for any Molecular Biology Technique. |
| | LinkBack | Thread Tools | Display Modes |
|
#1
| |||
| |||
| Dear Tom, A while ago you posted a thread (see below), I was wondering if you could share the link to the protocol you used for the generate ssDNA. I have searched the web, but cant not find the protocol you mentioned Thanks, Priyesh Rughani Dear Colleagues, I have isolated mg quantities of ssDNA following the protocol of Gruber et al in Focus 15: 59-65. I have a problem in that the OD 260/280 is about 1.5 after following the full protocol. I need to quantify this material precisely as well as having very clean ssDNA. Does anyone have any quick solutions for a cleanup of this large amount of material. In the protocol, multiple phenol-chloroform extractions have already been performed. If there is a FAQ to this point could someone direct me to it. Thanks, Tom Newman |
| Tags |
| cleanup , ssdna |
| Thread Tools | |
| Display Modes | |
|
|
| | ||||
| Thread | Thread Starter | Forum | Replies | Last Post |
| running ssDNA (30-1000nt) in denatured conditions | TC | Protocols and Methods Forum | 1 | 11-19-2008 07:10 AM |
| Western Blot Woes - Very Clean Western | kiki06 | Western Blot Forum | 3 | 07-22-2008 02:30 PM |
| Poor resolution when isolating ssDNA? | Evan Reed | Protocols and Methods Forum | 1 | 06-17-2008 06:12 AM |
| 'clean, fresh scent'? | louis | Chemistry Forum | 1 | 02-21-2004 07:50 PM |
| FS: Old Physics-Related Books | Oldbooks78 | Physics Forum | 0 | 08-27-2003 02:32 PM |