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Thread | Thread Starter | Forum | Replies | Last Post |
QC steps in Mate Pair Library Prep | busypops | SOLiD | 0 | 05-02-2011 02:33 AM |
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Mate-pair library prep for Illumina | bkingham | Sample Prep / Library Generation | 0 | 08-09-2010 07:56 AM |
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#1 |
SteveL
Location: San Diego Join Date: Sep 2009
Posts: 6
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Hello all,
I have prematurely run out of the three buffers that come with Illumina's Mate Pair Library Prep Kit. Specifically, they are:
All the best, Steve |
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#2 |
Senior Member
Location: Monash University, Melbourne, Australia. Join Date: Jan 2008
Posts: 246
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Have you tried asking illumina tech support?
I don't have recipes for these exact buffers, but you can find the recipes for other companies' streptavidin magnetic bead washing buffers on the web. Often they're just PBS pH 7.2 with 0.01% tween-20... but often they're using bound antibodies rather than DNA. |
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#3 |
Member
Location: Rochester,MN Join Date: Jan 2008
Posts: 15
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Did you ever find out what these were. My Mate pair kit is on backorder and I am trying to by reagents separately. I am also trying to which DNA Exonuclease they use.
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#4 |
SteveL
Location: San Diego Join Date: Sep 2009
Posts: 6
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I eventually got the dynabeads kilobase binder kit from invitrogen since I was doing long insert preps. I substituted the illumina binding protocol for the invitrogen on at the binding stages. I'm not sure this is what you're looking for, though.
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#5 |
Junior Member
Location: boston Join Date: Apr 2009
Posts: 2
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I really need to know what exonuclease is used following circularization. I used up all mine experimenting with this step and don't want to choose the wrong one. Anyone know an appropriate exo to use?
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#6 |
SteveL
Location: San Diego Join Date: Sep 2009
Posts: 6
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I talked to someone from NEB about digesting linear DNA only (and not circularized DNA), and they recommended Lambda Exonuclease (M0262S).
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#7 |
Junior Member
Location: Brazil Join Date: Mar 2010
Posts: 4
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Does anybody know about the buffers?
What´s the difference between the wash buffers 1 and 2? |
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