Or you could just add dnase/ benzonase for 5 minutes and use lysozyme for protein isolation from IBs much gentler.
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On Tue, 21 Nov 2017 at 3:01 am, DK<dk from no.email.thankstospam.net> wrote: In article <mailman.123.1510862205.15473.methods from net.bio.net>, Megha Goyal <mgbiotec from gmail.com> wrote:
>yes we also assume the same. so any suggestion how can we handle it. Our
>protein is in form of inclusion bodies and we get our protein but slimy
>cell mass makes it difficult to handle the cell paste.
If it's in IBs then who and why cares about the "slime"? You'll need to
sonicate/French press anyway and that breaks up DNA nicely. I'd suggest
sonication (looooong sonication) after every pelleting/wash cycle. That's
the right thing to do when cleaning up IBs for refolding anyway.
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