SYNTHESIS OF OLIGODEOXYNUCLEOTIDES CONTAINING N-4-MERCAPTOETHYLCYTOSINE AND THEIR USE IN THE PREPARATION OF OLIGONUCLEOTIDE-PEPTIDE CONJUGATES CARRYING C-MYC TAG-SEQUENCE
D. Gottschling et al., SYNTHESIS OF OLIGODEOXYNUCLEOTIDES CONTAINING N-4-MERCAPTOETHYLCYTOSINE AND THEIR USE IN THE PREPARATION OF OLIGONUCLEOTIDE-PEPTIDE CONJUGATES CARRYING C-MYC TAG-SEQUENCE, Bioconjugate chemistry, 9(6), 1998, pp. 831-837
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear",Biology,"Biochemical Research Methods",Chemistry
The preparation and properties of oligodeoxynucleotides containing mer
captoethyl groups at position N-4 of cytosine are described. The resul
ting thiol-oligodeoxynucleotides were reacted with a maleimido-peptide
carrying the c-myc tag-sequence. The peptide-oligonucleotide conjugat
e is specifically recognized by an anti c-myc monoclonal antibody, thu
s constituting a labeling system with sensitivity similar to other exi
sting methods of nonradioactive labeling.