Low DNA yield for Gecko V2 library prep?

567 views
Skip to first unread message

JP

unread,
Jul 20, 2015, 8:42:07 PM7/20/15
to cri...@googlegroups.com
I followed the protocol for Gecko library prep and achieved excellent transformation efficiency using Endura cells (lentiGuide-puro library A). But when I apportioned the bacterial pellet into 0.45 g aliquots as recommended by the protocol onto six maxiprep columns, the DNA yield was only 100-300 ug plasmid per each. I would expect about 1 mg of plasmid DNA per gram of bacteria, and I only achieved about a third of that (~0.33 mg plasmid / gram of wet bacterial pellet.)

Does anyone else have experience prepping this library?

Katie

unread,
Jul 23, 2015, 2:57:26 PM7/23/15
to Genome Engineering using CRISPR/Cas Systems, jhnwph...@gmail.com
I received good yield for the A and B libraries, 1.23mg and 1.62mg. I used the NEB alpha electrocompetent cells with the biorad electropulsar and grew them on the very large bioassay plates, as the protocol says, I used the Qiagen Maxiprep kits

JP

unread,
Jul 23, 2015, 3:56:15 PM7/23/15
to Genome Engineering using CRISPR/Cas Systems, williamskat...@gmail.com
How many prep columns did you use per plate?
Message has been deleted

Charlotte

unread,
Oct 23, 2015, 8:55:34 AM10/23/15
to Genome Engineering using CRISPR/Cas Systems, williamskat...@gmail.com
Hello JP,

I am having similar problems with the amplification of GeCKO v2 library. Did you solve your problems already? And if so, could you please share your solutions.

Joydeep Bhadury

unread,
Oct 23, 2015, 10:17:56 AM10/23/15
to Genome Engineering using CRISPR/Cas Systems, williamskat...@gmail.com
Hi 
I got a pretty decent yield for the Mouse GeCKO v2 lib A. 
I used the Endura cells for transformation and Cfu were really high. Then i snap freezer the pellet (1.45g wet pellet). In theory i was suppose to use around 3 maxi prep column , but i only had midi-prep kit ( Qiagen Midi plus). So i just used 5 midi columns and eluted the samples. Pooled the five preps and i got ~900ug/ul conc in a total vol of 1ml. I made virus and the titre was pretty good .

Hope this helps

BR 
Joy

Junjie Wu

unread,
Dec 17, 2018, 5:04:27 AM12/17/18
to Genome Engineering using CRISPR/Cas Systems
Hi Joy, 

In this post you mentioned to use 3 maxi prep columns for 1.45 g wet pellet, and I think I got the same info on this forum from another post. However, based on qiagen protocol, a maxi prep is only good to handle 100 ml culture with high copy plasmid (GECKO V2 is high copy). Assuming 3g pellet / 1 liter culture, it would be 0.3 g pellet for 100 ml culture for one maxi prep (QIA TIP 500). Then, 1.45 g pellet would require 5 maxi prep columns. Am I right? 
In the case of low-copy plasmid, however, it is 500 ml culture (1.5 g pellet) per maxi prep column. 
Thanks.

Junjie
Reply all
Reply to author
Forward
0 new messages