Go Back   Molecular Biology Forum > Molecular Research Topics Forum > Molecular Biology Techniques > DNA Techniques
Register Blogs FAQ Members List Calendar Science Groups New! Arcade Search Today's Posts Mark Forums Read

DNA Techniques Post questions and discuss DNA techniques and protocols such as DNA extraction, PCR, and the study of DNA-binding proteins.


pGEX 2T vector maxi prep or mini prep

DNA Techniques

Post questions and discuss DNA techniques and protocols such as DNA extraction, PCR, and the study of DNA-binding proteins.



Register Molecular Biology Forums
Reply
 
LinkBack Thread Tools Display Modes
  #1 (permalink)  
Old 02-12-2008, 07:17 PM
Pipette Filler
Points: 318, Level: 6Points: 318, Level: 6Points: 318, Level: 6
Activity: 0%Activity: 0%Activity: 0%
 

Join Date: Nov 2007
Posts: 4
david1259 RSS Feed
Default pGEX 2T vector maxi prep or mini prep

I need to seqeunce my two DNA in pGEX-2t vector in BL21 cells.
I tried to mini prep and Maxiprep however the DNA conc is too low to sequence.
Is there any way I can increase DNA amount?


I usually use 1ml culture for miniprep or 50ml culture for maxiprep.

Please, help me.

Last edited by david1259; 02-12-2008 at 07:27 PM.
Digg this Post!Add Post to del.icio.usBookmark Post in TechnoratiFurl this Post!Spurl this Post!Reddit!
Reply With Quote
Alt Today
Advertising
Google Adsense
 
This advertising will not be shown
in this way to registered members.
Register your free account today
and become a member on
Molecular Biology Forum
Standard Sponsored Links

  #2 (permalink)  
Old 02-12-2008, 08:38 PM
Graduate Student
Points: 1,689, Level: 24Points: 1,689, Level: 24Points: 1,689, Level: 24
Activity: 8%Activity: 8%Activity: 8%
 

Join Date: Aug 2006
Location: Ithaca, NY
Posts: 123
kmunson779 RSS Feed
Default Re: pGEX 2T vector maxi prep or mini prep

1) I would not suggest using BL21 cells to propagate plasmids. They're not as good as DH5a (for example) at avoiding DNA recombination and mutation issues.

2) I use 5 mL of culture for a miniprep and 50 for a midiprep -- for high copy plasmids, the Qiagen maxi kits take 100 mL of culture. You could try scaling up.

3) If it's simply a concentration issue rather than yield, an ethanol precipitation step will give you higher concentration plasmid.
Digg this Post!Add Post to del.icio.usBookmark Post in TechnoratiFurl this Post!Spurl this Post!Reddit!
Reply With Quote
Reply

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Trackbacks are On
Pingbacks are On
Refbacks are On
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Mini Prep princezz DNA Techniques 2 11-26-2007 09:55 PM


All times are GMT. The time now is 07:26 AM.


Powered by vBulletin® Version 3.7.1
Copyright ©2000 - 2008, Jelsoft Enterprises Ltd.
Copyright 2005-2007 Molecular Station | All Rights Reserved