Hi all,
Any of you got some experience on purifying (and crystallizing)
VIL-rich proteins (actually, more particularly isoleucine rich). Tried
to purify my protein, but majority (if not all) of the proteins reside
in the inclusion bodies. Induction is at low temperature, overnight
and
published examples? Any
suggestions on the detergent type/concentration would be welcome.
Thanks,
Vitali
--
Allan Pang
Visiting Scientist
G35 Joseph Priestley Building
Queen Mary University of London
327 Mile End Road
London, UK
E1 4NS
Phone number: 02078828480
Twitter: @xerophytes
recipient, please contact the sender and delete
this message. Any unauthorized use of the information contained in
this message is prohibited.
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Twitter
this protein for crystallography
is not desirable .
best regards
Amr
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Twitter: @xerophytes
check the formation of disulphide bonds
in protein. Additionally, does anybody knows another method(s) that can be
used to trap a closed conformation. I look forward for your suggestions and
discussions on this issue.
Thanks very much!
Jan
--
Allan Pang
PhD Student
G35 Joseph Priestley
and not
expressly made on behalf of the NIAID by one of its representatives.
**
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Twitter: @xerophytes
transfer.
Thanks!
Allan
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Twitter: @xerophytes
Research Scholar, Brandeis University
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Twitter: @xerophytes
that these amino acids are not residues found in the
N-terminal region or anywhere else in the protein.
Allan
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
://xtaldave.posterous.com/ (less sensible)
Twitter: @xtaldave
Skype: DocDCB
On 28 August 2011 10:25, Allan Pang a.p...@qmul.ac.uk wrote:
Hi there everyone,
What does it mean when you have proteins eluting in almost the whole
column
volume of S200?
I ran a gel with fractions from
concentrated
and loaded on a gel filtration column Superdex-200, they elute in the void
volume. But the proteins donot precipitate out !!
Is it worth while to go ahead for crystallization trials??
Any other suggestion is most welcome.
Thanks
Anita
--
Allan Pang
PhD Student
G35 Joseph
.
Cheers,
Allan
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
!
Thanks,
Allan
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
Phone number: 02078828480
Centre for Treatment, Research and Eduction in Cancer (ACTREC)
Tata Memorial Hospital, Kharghar, Navi Mumbai-410210 *
#
--
Allan Pang
PhD Student
G35 Joseph Priestley Building
Queen Mary University of London
London
E1 4NS
14 matches
Mail list logo