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Recovering transformed cells from Soft Agar

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Amtekoth
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Topic Started by Amtekoth
on 1/1/2009 8:33 AM   
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I've transformed human PBMCs with a virus and plated in soft agar (agarose, not low melt).

Colonies grew and I pulled plugs with pipet tips, plating the plugs in media in a 96 well plate. I had to pipet up and down a lot, since the plugs frequently stuck to the inside of the pipet tip.

I'm not sure if my cells were able to escape the agarose. Since I want to grow up transformed colonies, how do I get them out of the soft agar and growing happily?

Dumb side question: I know you can use agarase to recover nucleic acids from agarose. Would that work or would it kill my cells?

Thanks,

Ed

"God put me on this earth to accomplish a certain number of things. Right now I am so far behind that I will never die."- Bill Watterson


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Carson O Genic
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Posted By Carson O Genic
on 1/1/2009 22:46 PM   
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I think if you break up the agarose enough that cell will find their own way out into the medium.

I'm not aware of any way to melt, even low-melting point agarose, and get viable cells out. I always use methylcellulose instead of agarose when I want to harvest colonies.



sjwilliams
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Posted By sjwilliams
on 6/7/2010 20:14 PM   
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You can recover both RNA, DNA and protein from colonies growing in agarose by using the Tri-Reagent LS (MRC) using their protocol for extracting nucleic acids from cells/tissue with high lipid/glycoprotein content.  Juset ask the tech services.  It works very well for RNA and DNA extractionProtein is a bit tricky but high abundant protein is easy.

Good luck



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