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#1
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| I am wondering why, when it comes to activated supports, etc, it is almost exclussively agarose/sepharose that is used. Almost never sephacryl. Even though sephacryls should be activatable by all the same chemistries available for agaroses... Why? Can anyone think of a GOOD reason for that? I would have thought that extremely high porosity of Sepharcyls S500 and S1000, coupled with their high rigidity and flow rates, will result in sorbents with higher capacity and, perhaps, less non-specific binding. Is this thinking wrong? If yes, why? Thanks for any comments, Dima |
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#2
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| Hi Dima, probably this is because most people (have to/want to) stick to established and traditional methods. Those companies who offer the corresponding kits don't need to change their ingredients as long as the existing ones are selling well. Patent issues should be another reason why not all possible combination researchers may think of are available on the market. And in the time of 'publish or perish' none of those who need to apply the methods dares to develop new ones. Also because it becomes more and more difficult to combine the necessary expertise for such developments in one research lab/setting due to its commonly high specialization. just some thoughts, Wolfgang BTW How do you limit shelf-live of your messages? |
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#3
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| In article <[Only registered users see links. ]>, WS <[Only registered users see links. ]> wrote: Well, I asked for a *good* reason :-) That's not quite it. Basically, I am trying to understand why Pharmacia itself never sold any form of activated or ligand-coupled Sephacryl and is selling a dozen of various activated and affinity sorbents based on Sepharose. OR: If we are to spent some time and money optimizing a home-made affinity matrix (all the way through - activation, linker, coupling), would we be better off starting with Sephacryl or Sepharose? I don't. Google does. I include the "X-No-Archive: Yes" header in my messages. Just a matter of principle because I don't like databases of any kind. In the old times, before Google started messing up with Usenet, this was honored by DejaNews and subsequently Google as a request of not showing up in their publically searchable database. Now Google shows it for some time (no idea how long) but then "deletes". DK |
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#4
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| Am 04.10.2008, 20:53 Uhr, schrieb DK <[Only registered users see links. ]>: Part of the reason may be that the old Pharmacia company no longer exists, it was bought first by Amersham and later by GE. It is quite possible that the expertise in separation technology once concentrated at Pharmacia has dispersed. The fact that the monographs on various separation techniques that Pharmacia used to offer for free are no longer maintained or even available (and it would be so cheap to put a pdf on their web-site) strongly points in that direction, as does the fact that we no longer hear about new techniques or matrices developed there. At least the Hoefer electrophoresis line is now rescued. Sic transit gloria mundi :-( |
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#5
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| On Oct 14, 3:48 pm, "Dr Engelbert Buxbaum" <[Only registered users see links. ]> wrote: .... I actually learned quite a bit from those booklets. Everything I needed to know about gel filtration I learned from Pharmacia ;-) Nick -- Nick Theodorakis [Only registered users see links. ] contact form: [Only registered users see links. ] |
| Tags |
| affinity , chtomatography , sephacryl , sepharose |
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| Thread | Thread Starter | Forum | Replies | Last Post |
| [Protein-analysis] Re: Affinity chtomatography - Sepharosevs Sephacryl? | Mark Nance | Protein Forum | 1 | 10-17-2008 01:26 PM |
| Affinity chtomatography - Sepharose vs Sephacryl? | DK | Protein Forum | 4 | 10-15-2008 05:02 AM |
| RE: Re: affinity columns (Allison) (DK) | Dan Guire | Protein Forum | 0 | 03-30-2007 10:35 PM |
| Re: affinity columns (Allison) | Dan Guire | Protein Forum | 2 | 03-30-2007 09:40 PM |