nality are you looking for?
Mike
Michael Giffin
The Scripps Research Institute
Department of Molecular and Experimental Medicine
10550 North Torrey Pines Road, MEM-131
La Jolla, CA 92037
email: mjgif...@scripps.edu
lab: 858-784-7758
On Wed, Jan 28, 2009 at 7:02 AM, Mark Collins
wrote:
>
the solution needs to be
> sufficiently dilute so that the chance of molecules "shadowing" one another
> is negligible. Isn't this condition violated for concentrated solutions
> (even with short path lengths)?
> Pat
> On 4 Dec 2008, at 1:27 P
name, concentration, and full spectra.
It is expensive, but so are good cuvettes.
Mike
Michael Giffin
The Scripps Research Institute
Department of Molecular and Experimental Medicine
10550 North Torrey Pines Road, MEM-131
La Jolla, CA 92037
email: [EMAIL PROTECTED]
lab: 858-784-7758
On Thu
gions of the
> vector onto the primers which also generate the initial PCR product. I plan
> to proceed with my insert which is ~ 2kb and am curious to get some feedback
> if you have successfully cloned inserts > 1.5kb using the above strategy.
>
> Many thanks.
> Raji
>
Micha
TED]> wrote:
> On 4 Apr 2008, at 01:36, Michael Giffin wrote:
>
>
> > i get the same error on OS X 10.5.2 and 10.4.11:
> >
> >
> > > sfcheck -f refmac2.mtz -m refmac2.pdb -out y -nomit 2 -map
> > >
> >
> > the error:
> > ---
i get the same error on OS X 10.5.2 and 10.4.11:
>sfcheck -f refmac2.mtz -m refmac2.pdb -out y -nomit 2 -map
the error:
Open failed: Unit: 11, File: sfcheck_scr.dat (logical: sfcheck_scr.dat)
Last system error message: Bad file descriptor
C
