Chris,  indeed nanoITC  instrument analysis software is very robust and user
friendly (probable more friendly than microcal, GE). 

Although when you need  to subtract  Q (heat)  values (from 2 or 3 blank
experiments) from your experimental data you cannot. NanoITC software  can
subtract  Q values only  from 1 blank experiment.
Also if you want to present  your data in a form of  heat/mol in Y
(vertical) axes  again you cannot. It presents  data in Y axes only in form
of heat/injection. 
If you have found a way to extract 2 or 3 blank experiments from
experimental data or present data in form of heat/mol, please let me know it
will be very useful.

The main problem in the output files from nanoITC come with an extension
.nitc, by default.  Unfortunately Origin (that can do all the above) can
read only,  filenames with an extension .itc

Cheers,

George

-----Original Message-----
From: Colbert, Christopher [mailto:[email protected]] 
Sent: Saturday, March 23, 2013 5:56 PM
To: George Kontopidis; [email protected]
Subject: Re: [ccp4bb] Isothermal titration calorimetry


George, would you please explain your comments?  We've found the TA
Instruments analysis software very robust and user friendly.

We have the low volume nanoITC from TA instruments and get equivalent #'s in
our comparison tests to the Microcal instrument.

Cheers,

Chris


--
Christopher L. Colbert, Ph.D.
Assistant Professor
Department of Chemistry and Biochemistry North Dakota State University P.O.
Box 6050 Dept. 2710 Fargo, ND 58108-6050
PH: (701) 231-7946
FAX: (701) 231-8324





On 3/23/13 8:47 AM, "George Kontopidis" <[email protected]> wrote:

>Keep in mind that output files from  nanoITC, TA instrument cannot be 
>red by Origin.  At some point you will need to analyse your data 
>further.
>
>George
>
>-----Original Message-----
>From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of 
>Anastassis Perrakis
>Sent: Saturday, March 23, 2013 12:46 PM
>To: [email protected]
>Subject: Re: [ccp4bb] Isothermal titration calorimetry
>
>It might be worth to consider the question more in detail.
>
>Do you want to study thermodynamics of the interaction, or a KD would do?
>If
>the former, you need ITC. If the latter, and you want to study things 
>at the level of KD only, maybe investing on a plate reader, 
>thermophoresis, or some biosensor technology (spr or interferometry 
>based systems) should be considered.
>
>Then, what interactions will you study with the ITC? In general, I 
>would agree that the lower sample volume is worth the nano options, but 
>depending on the typical systems under study, sometimes the gain on 
>sample quantity is not worth the money - while many times its worth it.
>
>John is if course right that for studying specific systems as the one 
>he describes the 200 is great.
>
>A. 
>
>Sent from my iPhone
>
>On 23 Mar 2013, at 11:00, John Fisher <[email protected]> wrote:
>
>> I would recommend the Microcal ITC 200, hands down. Not only is it an
>amazing instrument with the optional automated sample loader (which is 
>worth every penny), but we were able to do experiments (multiple) using 
>FULL-LENGTH p53 binding to a weak cognate protein. I believe this was 
>the first time ITC was ever used with full length p53, as it is so 
>labile and just loves immediately to oligomerize. Sample sizes pay for 
>the instrument.
>> Best,
>> John
>> 
>> John Fisher, M.D./PhD
>> St. Jude Children's Research Hospital Department of Oncology 
>> Department of Structural Biology
>> W: 901-595-6193
>> C: 901-409-5699
>> 
>> On Mar 23, 2013, at 4:45 AM, Sameh Soror <[email protected]>
>>wrote:
>> 
>>> Dear All,
>>> 
>>> 
>>> I am sorry for the off topic question. I am going to buy ITC to 
>>> study
>protein-protein & protein-ligand interactions....
>>> 
>>> I am comparing microcal, GE and nanoITC, TA instrument..
>>> any suggestions, recommendations, good experiences or bad experiences.
>>>is
>there a better system.
>>> 
>>> 
>>> Thank in advance for the help.
>>> 
>>> 
>>> Regards
>>> 
>>> 
>>> Sameh
>>> 
>>> --
>>> Sameh Soror
>>> 
>>> Postdoc. fellow
>>> 
>>> 
>

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