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Published byBuck Hodges Modified over 9 years ago
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Albinism
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Genetic Engineering Altering the DNA of a cell or organism
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G.E. Techniques
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DNA Extraction How do you get DNA out of a cell to work with? Cells cut open with enzymes DNA filtered out
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Multiplying DNA PCR = process for multiplying DNA DNA + Enzymes + Nucleotides mixed in test tube Placed in “PCR machine” to regulate temp.
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PCR
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Kary Mullis – Invented PCR Won Nobel Prize in 1993
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Cutting DNA DNA molecules too large to work with Can be cut up using Restriction Enzymes - They cut DNA at specific nucleotide sequences
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Restriction Enzymes
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DNA Analysis Gel electrophoresis – separates DNA fragments for analysis
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Gel Electrophoresis Think jell-o
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Gel Electrophoresis Gel is sponge-like DNA neg. charged
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Gel Electrophoresis DNA has a (-) charge, moves to (+) end of gel Small pieces move in gel farther than large DNA separated by size and charge
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*Bands on gel are DNA - + Ethidium bromide
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Genetic Engineering Uses
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Gel Elec. and Paternity Testing If people related, DNA is similar REs will cut a similar pattern, can be analyzed on gel
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Cloning Ian Wilmut - cloned Dolly the sheep Nucleus from 1 sheep put into egg of another Embryo inserted into foster mother to develop
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Plasmids Plasmids – circular DNA molecule, found in bacteria
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Plasmids Plasmid cut open with REs Gene of interest inserted into plasmid Recombinant DNA – DNA from 2 organisms combined
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Plasmids Next, plasmid placed into bacteria cell Protein synthesis of gene carried out What could be a use of this technique? Ex. Diabetes
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Diabetics unable to produce insulin Insulin gene inserted into plasmid and bacteria produce it for them
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Firefly Luciferase
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