Answer Posted / neha
Phenyl isothiocyanate reacts with free amino grp of
aminoacid or peptide under alkaline condition to form
phenyl isothiocarbomyl derivative or peptide which inturn
release water molecule in presence of Hcl to form
phenylthiohydantoin(PTH) & release remainder of peptides
for second reaction.
This reaction is also used to identify N-terminal
aminoacid in protein sequencing method
Is This Answer Correct ? | 7 Yes | 1 No |
Post New Answer View All Answers
What are the important sources of phosphorus?
How do you define free radical addition reaction? Give an example.
To what organic group do pentoses belong?
Give the chemical formula of Garnet?
Why the transition metal ions or compounds exhibit color?
In double bond, how many sigma and Pi bonds are present in it?
I understand that urine can act as a reagent to break disulfide bonds? I am particularly interested in bonds between cysteines. and or any other amino acids.
What are respectively some remarkable functions of myosin?
Which are the nucleotides “portions” that bind in the formation of nucleic acids?
Does ph affect the enzyme activity?
why we use 96 well plate in ELISA plate reader?
What are allosteric enzymes?
To calculate the e.m.f of the cell when does the nelsons equation is use?
give the co-ordination number of nacl?
give the formula of borax. Borax is chemically called as.