Abstract
Mercury orange dissolved in a mixed solution of acetone and KH 2 PO 2 NaOH buffer reacted rapidly and specifially with SH groups in proteins. The combined Mercury orange was eluted quickly in acidic acetone, which directly reflects the number of SH groups. The procedure is applied for the measurement of SH groups in both soluble and structural proteins.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
