Kits d'expérimentation, clonage bleu/blanc d'un fragment d'ADN et dosage de la ß-galactosidase
Catalog # EDVO300
Supplier: EDVOTEK
Specifications
- Désignation:Clonage bleu/blanc d'un fragment d'ADN et dosage de la ß-galactosidase
- Environmentally Preferable:
- Cdt:1 KIT
Specifications
About this item
When DNA is subcloned in the pUC polylinker region, β-galactosidase production is interrupted, resulting in the inability of cells to hydrolyse X-Gal. This results in the production of white colonies amongst a background of blue colonies. This experiment provides a DNA fragment together with a linear plasmid and T4 DNA ligase. Following the ligation to synthesis the recombinant plasmid, competent E. coli cells are transformed and the number of recombinant antibiotic-resistant white and blue colonies are counted. β-galactosidase activity is assayed from blue and white bacterial cells.
- For 5 lab groups
- Ligation 60 minutes; transformation 40 minutes; incubation overnight
Autres éléments nécessaires : incubateur, bains-marie, micropipette automatique et pointes, spectrophotomètre, centrifugeuse et microcentrifugeuse.
Delivery: Kit includes instructions, linearised pUC plasmid and DNA fragment, T4 ligase, bacterial LyphoCells for transformation, reconstitution buffer, X-Gal in solvent, IPTG, calcium chloride, antibiotic, ReadyPour LB agar, LB media for recovery, growth media, assay components, and plastic supplies.