Dear all,

A note on high pressure homogeniser designs.

Clogging is the main problem with all fixed geometry disruption channel 
instruments. When selecting a cell disruptor for my laboratory I came across 
the Stansted high pressure variable geometry chamber homogeniser. The 
"disruption" gap is formed between the conical surface of the chamber and a 
needle on an "air suspension". This solution allows particles to push the 
needle off and temporarily widen the chamber gap, preventing blockages.

We have not had a single clogging incident with their SPCH-10 homogeniser after 
3 years of use.

https://www.homogenisingsystems.com/laboratory_high_pressure_homogenizers.html





Oleksiy
sent from mobile

On 25 Mar 2025 8:44 am, M T <michel...@gmail.com> wrote:
Dear Cyprian,

I recommend to users to use a Potter-Elvehjem homogenizer before to use the 
LM20, or even (in case of non fragile protein) to do some cycle of sonicator.

I advice also to pay attention to the anti-drop ring of the used bottle. 
Because in case of old one, you may have some plastic particles which falls in 
the sample and clog the LM20 cell. Of course, dust is not welcome neither…

To unclog the cell there is no other choice than to invert it. In case of 
severe clogging, the water-bath sonicator can help (gentle heating and 
sonication), before to retry to unclog the cell mounted in a reverse way.

Best.

Michel.

Le 25 mars 2025 à 07:09, Cyprian Cukier <cyprian.cuk...@selvita.com> a écrit :



Dear Community,



First of all, apologies for the slightly off-topic question, which is related 
to protein purification rather than crystallography.



I am seeking your advice on preparing the cell pellets for the lysis process. 
We have an LM20 microfluidizer and we experience quite frequent clogging of the 
system that is tedious to remove. This happens particularly with the E. coli 
pellets, but from time to time the eukaryotic cells are also problematic. Does 
anyone have well-established protocols on how to handle the cell pellets before 
applying them to the lysis process in the microfluidizer?



I should add that of course we follow the manufacturer's recommendations to 
have a homogenous suspension, which is not too dense.



I would also appreciate any advice on how you clean your systems (regularly or 
in case of clogging).



Best regards

Cyprian

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