data quality is not good and
twin. We tried to produce SA-omit map using phenix. The map is really bad. Does
anyone have suggestion to refine the map? Thank you!
Bests,
zq Deng
2013-11-04
dengzq1987
Hi all,
recently, i perform an EMSA experiment.when i prepared the DNA with a 5'
poly(G)-tailed ,i find that it formed guanine tetraplexes .how can i prevent
this happen,or has any method to disrupt the guanine tetraplexes structure?
any suggestion is appreciation.
dengzq
Hi all,
recently,I want to use DelPhi to calculate the Electrostatic potentials of
DNA.but in the manual,i can not find the method to create the inputfile fort.11
、fort.12 and fort.13.Does anyone have experience on this? Please suggest
Thank you in advance
Sincerely
dengzq
Hi CCP4bb,
I have two dataset from one crystal with different distance.now i am wondering
how to merge the two dataset into one file,and use it to refinement.
thanks a lot!
deng
Hi all,
I got a protein-DNA complex crystal,by running SDS-PAGE and nativePAGE,i prove
that the crystal contain both
protein and DNA.BUT it does not diffract. does anyone have suggestion to
improve the diffraction ability ?
Best wishes,
deng
Dear all,
Recently, I used MOLREP to molecular replacement.
My OS is fedora 14 and CCP4 version is the newest one ccp4-6.2.0 .
When I run a pdb file and mtz by MOLREP without input fixed model, everything
is right.
However, when I run it by MOLREP when using "input fixed model".
The erro
hello all,
is there any screen kit that is highly effective for the crystallization of
protein-nucleic acids complexes?
deng.
my crystal is not plate.it is Hexagonal and very large.
2011-04-05
dengzq1987
发件人: Jacob Keller
发送时间: 2011-04-05 20:53:41
收件人: CCP4BB
抄送:
主题: Re: [ccp4bb] how to Collecting Data from Long Unit Cell Axes ?
For plate crystals with the long axis normal to the plate surface
od to solve this problem?
best wishes.
2011-04-05
dengzq1987
Dear all,
Recently,i purchase Oligonucleotide from company.the sequence is
TTGCGTAC GCAC GTACGC .i want to perform self-annealing process to form
the following second structure .
5' TTGCGTACGC
||| |||]
3' CGCATGCA
i hope that most of
thank you!
2010-10-31
dengzq1987
stock solution
has free pi ,maybe the ATP hydrolysis when prepared .any suggestion about
preparing ATP stock solution is appreciative.
Best regards!
2010-08-29
dengzq1987
the
standard value by CaCl2 and EDTA titration or NaHCO3 and HCl titration.
Can Nano ITC low volume (190 ul) be used for measuring protein interaction?
Any suggestions are very appreciated.
Thanks
2010-07-23
dengzq1987
protein to do
zinc scan,we don't find the zinc. does anyone have some advice?
2010-03-31
dengzq1987
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