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Nature 2013 Idris et al However I don't understand the chemistry at the molecular level and am hoping someone more knowledgeable can help
However, our company INTCO has several machines which can deal with the problem PNAS 2012 Aldridge and Hadfield

Smaller fragments are retained in the buffer usually discarded and so you can get different size ranges from a single sample with multiple purifications.

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comment choisis tu les albums sur lesquels tu travailles? Anonymous Please bear with me as this is entirely new to me
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PEG causes the negatively-charged DNA to bind with the carboxyl groups on the bead surface
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: Bonjour, Super tous tes docs! And then we can reuse the resources to do other products such as floor bricks
Merci Bonjour Corinne, Quel plaisir ton site! Side note, smaller nucleic acid polymers are more soluble in these alcohol solutions due to their smaller size - form smaller condensed balls Molecular Cell 2008 Smith et al
The final DNA product is eluted from beads for further processing e The size of fragments eluted from the beads or that bind in the first place is determined by the concentration of PEG, and this in turn is determined by the mix of DNA and beads

Substituting size-fractionated silica particles for diatoms the fossilized cell walls of unicellular algae allowed for the purification of microgram amounts of genomic DNA, plasmid DNA, and rRNA from cell-rich sources, as exemplified for pathogenic gram-negative bacteria.

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Seems reasonable, depending on the pH, and assuming that the phophoryl groups of the DNA backbone remain deprotonated whilst the carboxyl groups of the beads are mostly protonated
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James has two kids and lives in Norfolk, which is a lot nearer the coast than Cambridge