Sanjaya N. Joshi
sanjay at hobbes.chmc.org
Thu Jun 1 18:27:32 EST 1995
I think "rasmol"
ftp forte.mathematik.uni-bremen.de /pub/unix/visualization/rasmol
ftp ftp.uni-stuttgart.de /pub/scivi/chemie/rasmol
will do that (at least the ribbon, ball-stick) for the H bonding part. It
will even save the 3D "pdb" file image as a GIF file..
_________ _________ ____sanjay at hobbes.chmc.org_________
/ /| / /|
/ / | / / | Sanjaya Joshi
/--------/ | /--------/ | Department of Radiology, CH-69
| | <|------| | | Children's Hospital & Med. Ctr.
| A |--/----->| B | / Seattle, Washington 98105
| | / | | / (206) 528-2744
And networks for all ................................................
On 31 May 1995, Roy Kimura wrote:
> In article <pharmscience.11.2FCA6EFA at gandalf.otago.ac.nz>,
> pharmscience at gandalf.otago.ac.nz wrote:
> > In our lab we have had a continiung problem with peptides adsorbing to glass-
> > ware. Suggestions to overcome have included washing the containers with a
> > surfactant, adding a competing protein (eg 2% BSA), or working at
> > (higher) concentrations where losses that do occur are negligible.
> > None of these suggestions however are satisfactory for the system we are
> > using.
> > Could anyone help us with other suggestions?
> > Reply to leo.schep at stonebow.otago.ac.nz
> One suggestion I have come across in the literature is to siliconize
> all glassware (something like Sigmacote from Sigma Chemicals; St. Louis
> USA). This seemed to work for my protein, although I never checked the
> loss of protein compared to non-siliconized glassware.
> Roy Kimura
> Dept. of Chemical Engineering
> Northwestern University
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