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Includes materials for five labsTransformation, a basic principle of genetic engineering, is investigated in this lab.
Students take the bacteria E. coli JM 101, which is sensitive to ampicillin and incapable of producing beta-galactosidase needed for lactose breakdown, and transform it by inserting the pUB8 plasmid. The bacteria thus receives antibiotic resistance as well as lac+phenotype.
In two 45-minute labs the traits are transferred and the transformed cells are grown on agar plates containing the antibiotic and on plates with ampicillin and x-gal, a histochemical substrate for B-galactosidase which yields a blue precipitate upon hydrolysis. Transformations appear as white colonies on plates with ampicillin, and blue colonies on plates with ampicillin and x-gal.
Includes: materials for five labs (recommended six students each)
, teacher's guide, student study and analysis copymasters with background information, time requirements, instructions, data table for analysis, and study questions.
An incubator and microcentrifuge are required for this experiment
Note: Live materials (67498-01) are required but not included.
The live materials set Includes the reagent set, E. coli, and plasmid DNA. A ship date is required.
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