Hello

I am working on a recomnibant protein, after its solublization i refolded the protein by using buffers of different composition and pH. In order to determine which buffer is resulting in the proper refolding of my protein by using the method defined in this article:

https://www.nature.com/articles/srep18906

and have used stepone qPCR machine for melt curve.

Later i analysed the data using Protein thermal shift software. I am confused whether i am going in the right direction or qPCR machine generated data should be analysed by any other software. In the above mentioned article thermo Q was used, however this software is not  free to download that why i have used Portein thermal shift software v 1.3. Is it Ok to present the figs generated by Protein thermal shift software ?

Thanks

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