On Thu, Mar 15, 2012 at 11:14 AM, Jon Agirre wrote:
> The best reproduction I can suggest would be to setup one or two LCP
> experiments exchanging the protein for its buffer. If you get crystals, you
> know for sure they're not protein.
It should be pointed out that the converse is not true:
The best reproduction I can suggest would be to setup one or two LCP
experiments exchanging the protein for its buffer. If you get crystals, you
know for sure they're not protein.
Cheers,
Jon
2012/3/15 Theresa H. Hsu
> Hi all.
>
> I set up some trays of membrane protein remotely in cubic phase
Hi Theresa,
Your observation of colored crystals under polarising lights seems odd to
me. I assume your protein should be colorless and under normal light these
crystals are colorless? Are these trays set up in glass plate or plastic
plates? If you are willing to upload some pictures, I might be ab
Hi all.
I set up some trays of membrane protein remotely in cubic phase. I don't have
ready access to them so I can't shoot/pick the crystals. Under polarising
lights, some crystals appears coloured across many conditions, making me think
these are salt. Is there some knowledge of inorganic che
