11 Questions 27 Answers 0 Followers
Questions related from Nii Sama
Hello I have done a cloning and after that i have stored my recombinant E.coli cells in the -80C and -20C as a cell banks. after i have used the cells for expression i saw a basal expression in...
11 November 2017 4,649 13 View
Hello.I have purified my protein with Ni-NTA coulmn and i have run my purified fractions on SDS-PAGE but i don't know how to calculate the purity of may bands. how should i do this?Thanks in advance.
07 July 2017 3,194 8 View
HelloI am trying to purify human growth hormone with His6 tag. thus i should make buffers with different imidazole concentration. i made my buffer solution at room temperature. but when i put...
02 February 2017 7,323 10 View
Hello dears. CLIQS(stands for Core Laboratory Image Quantification Software) from totallab company is one of the gelanalyzer software like ImageJ but i want some tutorial to learn it well( any...
11 November 2016 6,012 0 View
Hello How do I ensure that my sonication has been done perfectly and my cell pellets were lysed completely?Any test or procedure? Thanks in advance.
11 November 2016 3,614 4 View
Hello I want to work on production of a recombinant protein(recombinant human growth hormone) in a laboratory and the answer of this question is very important to me. Is it Possible that after...
10 October 2016 7,545 8 View
Hello dears. I did run SDS-PAGE gel yesterday, after staining the gel and destaining the gel i saw that protein's bands did not migrate to the end of the gel and they have just migrated half of...
07 July 2016 3,858 7 View
Hello I want to plot my chrmatographic column's chromotoramme but i don't have access to HPLC system and i dont know how to get my protein peak therefore i should make my own chromotogramme...
07 July 2016 5,499 10 View
Hello Why do we use Amino Acids in culture medium, i mean what is the mechanism of used amino acids in molecular point of view? What is they role in cell mechanism? any publication? Thanks in...
02 February 2016 8,261 2 View
Hello I don't understand the relation between reagents used in SDS-PAGE making. I mean there are many protocols that say how to make SDS-PAGE, for example 15%, but they don't mention how they...
01 January 2016 1,844 4 View
Hello which methods are good to disrupt the E.coli periplasmic space to extract protein and what is the mechanism of each method? Thanks in advance.
01 January 2016 3,371 6 View