is used to isolate
fluorescently labeled from unlabeled peptide. In addition, determining
the proteolytic cleavage of pattern of proteins is used to monitor
stable regions of proteins.
||Steady State Fluorescence
Instrumentations provides sensitive measure of complex systems.
fluorescence at high pH demonstrates several distinct
|Circular Dichroism Spectrometer
Analysis of protein secondary structure is commonly accomplished by measuring the far ultraviolet chiral absorbance of the peptide backbone. The folding of proteins can be precisely followed.
|Stopped Flow Instrumentation
Millisecond resolution of enzyme kinetics are done with an OLIS RS-1000 multi-wavelength Stopped-Flow instrument. Single Value Decomposition (SVD) software allows the determination of rate constants and identification of species in a complex reaction.