A collegue of mine is looking for a quick and easy way of extracting C.
elegans proteins into buffer.
He claims that, in his previous attempt, C. elegans worms survived polytron
homogenisation and sonication in a triton X-100 buffer (i.e. there were
still some worms intact and ALIVE post-treatment).
Is there a more succesful technique?
Cheers,
Stuart.
+-------------------------+--------------------------------------+
| Stuart Rison | Ludwig Institute for Cancer Research |
| Tel. (0171) 878 4127 | Courtauld Building |
| Fax. (0171) 878 4040 | 91 Riding House Street |
+-------------------------+ London, W1P 8BT |
|stu...@ludwig.ucl.ac.uk | UNITED KINGDOM. |
+-------------------------+--------------------------------------+
- And there's a NO_JUNK bit to remove in my return address -
Yeah, they're tough little buggers.
> Is there a more succesful technique?
I used a French press set at 5,000 psi internal pressure.
good luck,
--
John Lye
e-mail to: rj...@Virginia.EDU
homepage: http://avery.med.virginia.edu/~rjl6n/homepage.htm