Utilisateur
RECOMBINANT DNA TECHNOLOGY
1973 by HERBERT BOYER AND STANLEY COHEN
pSC101
IT HAS A SINGLE REGION WITH GAATTC SEQUENCE AND THE PRESENCE OF TETRACYCLINE RESISTANCE GENE
PAUL BERG
ENZYME RESTRICTION ENDONUCLEASE, DONOR DNA AND VECTOR DNA
EcoR1
EcoR1
serves as a scissor that cuts the donor and vector dna at the very specific site that contains palindromes
PALINDROMES
STICKY ENDS
DONOR DNA
VECTOR DNA
PLASMID
PRESENCE OF ORIGIN OF REPLICATION AND HAS MARKERS THAT SERVES AS A GUIDE
GENETIC MARKERS
pBR322 and pUC18
Psti and BamHI
Psti
BamHI
pUC18
LACZ
GALACTOSIDASE
POLY LINKER
1. ISOLATE THE DONOR AND VECTOR DNA
2. CUT THE DNAs WITH RESTRICTION ENYME
3. COMBINE THEM WITH DNA LIGASE
4. HOST CELL TRANSFORMATION THROUGH CHEMICAL TRANSFORMATION OR ELECTROPORATION
5. RECOMBINANT DNA CLONING
6. SCREENING OF THE TRANSFORMED CELL (EX: BLUE WHITE SCREENING)
CHEMICAL TRANSFORMATION
ELECTROPORATION