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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Junior Member
Location: Kent Join Date: Oct 2008
Posts: 3
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I am trying to prepare multiple samples with Invitrogen's Sequalprep long range PCR kit for sequencing on a 454. Does anyone have any experience of this, for example how much do you need to quality control your PCR products (for specificity etc) before quantification and pooling?
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#2 |
Member
Location: Seattle Join Date: Mar 2008
Posts: 29
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Hi
I don't know about this and I'd like to hear if you find out. Can you please tell me how you process the PCR products for subsequent sequencing or can you point out literature? thanks vasvale |
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#3 |
Junior Member
Location: Kent Join Date: Oct 2008
Posts: 3
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I'm using the Sequalprep LR-PCR kit and Normalisation plates, then using Parallel Tagged Sequencing (Meyer et al 2008, Nat Protocols 3 (2) 267-278)
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#4 |
Member
Location: france Join Date: Nov 2008
Posts: 10
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Hi Ellenthomas !
Nice ! have you already started your test ? I'd like to hear more about that, may i will go in this way... |
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#5 |
Member
Location: france Join Date: Nov 2008
Posts: 10
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Hello
Which software will you use to design your primers for long PCR ? |
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#6 |
Junior Member
Location: Kent Join Date: Oct 2008
Posts: 3
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I just use Primer 3 which is free on the web. There are primer design instructions in the Sequalprep kit.
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#7 |
Junior Member
Location: Alberta, Canada Join Date: Jul 2009
Posts: 2
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Hi there,
I'm also using the SequalPrep Kit and I do a simple sanger sequencing of the ends of my fragment using my LR PCR primers to verify my fragments. |
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#8 |
Moderator
Cambridge, UK Community Forum Location: Cambridge, UK Join Date: Feb 2008
Posts: 221
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We are using SeqalPrep for lr-PCR and it is working. However there are lots of questions that we are thinking about as the read coverage is nowhere near smooth across the region and although I expected some varialbility I did not think it would be as high as it is.
JAmes. |
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#9 |
Member
Location: USA Join Date: May 2009
Posts: 37
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We're doing something different but also have a lot of problem with uneven non-random coverage. If anyone knows of any tweeks to smooth coverage I'd be interested to hear about them.
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#10 |
Junior Member
Location: Cleveland Join Date: Oct 2011
Posts: 2
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We've tried using this kit for enrichment of regions around 10-12kb. The efficiency for this was near zero. We downscaled it down to 3-7kb and are starting to get amplification efficiency around 30-50%.
For our purposes this kit is waste of money, especially because of i) the price, and ii) nonexistent customer support. We wrote several times to speak to people who actually KNOW how this kit works, but we got general answers about how to design primers..... Well, the best option for us would be raindance, but who can afford this... |
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#11 |
Senior Member
Location: London Join Date: Jun 2009
Posts: 298
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Any advice on how to purify LR-PCR products before shearing?
Would Ampure beads work or maybe Qiaquick columns? |
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#12 |
Member
Location: USA Join Date: May 2009
Posts: 37
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standard Sigma pcr cleanup columns and Clontech/Macherey-Nagel nucleospin columns have both worked fine for us to supply template to our core. i am pretty certain they do not do any further clean up prior to fragmentation.
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