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Mutat Res ; 262(3): 177-81, 1991 Mar.
Article in English | MEDLINE | ID: mdl-1848353

ABSTRACT

We used liposomes to deliver the restriction endonucleases BamHI and SmaI into human heteroploid HEp-2 cells. With this method very low concentrations of enzymes (2 units/ml) were active in the production of chromosomal aberrations. SmaI, which produces blunt-ended double-strand breaks in the DNA molecule, induces chromosomal aberrations more effectively than BamHI, which produces cohesive ends. Our results indicate that liposomes are suitable vectors for introducing restriction endonucleases into cultured human cells.


Subject(s)
DNA Damage , DNA Restriction Enzymes/pharmacology , Mutagenesis , Cells, Cultured , DNA Restriction Enzymes/administration & dosage , DNA-Cytosine Methylases/administration & dosage , DNA-Cytosine Methylases/pharmacology , Deoxyribonucleases, Type II Site-Specific/administration & dosage , Deoxyribonucleases, Type II Site-Specific/pharmacology , Drug Carriers , Humans , In Vitro Techniques , Liposomes
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