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Topic 6 (DNA Profiling (PCR (Cycle starts again with all 4 strands (2…
Topic 6
DNA Profiling
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PCR
- Reaction mixture is set up: DNA sample + free nucleotides + DNA polymerase + primers
- Mixture is heated to 95° - to break hydrogen bonds = 2 stands
- Mixture is cooled to 50-65° - so primers can anneal (bond) to strands
- Mixture is heated to 72° - so DNA polymerase can work
- DNA (Taq) polymerase lines up free nucleotides alongside each template strand using complementary base pairing = 2 new complementary strands
- Cycle starts again with all 4 strands (2 original, 2 new) used as templates and is repeated
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Gel electrophoresis
- DNA is places into a well in a slab of gel and covered in a buffer solution that conducts electricity
- An electrical current is passed through the gel
- DNA fragments are negatively charged – move towards the anode (+ electrode) at the far end
- Shorter DNA fragments move faster & travel further through the gel
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Forensics
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Decomposition
putrefaction
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microorganisms secrete enzymes that break down the dead organic matter into small molecules that they can respire
autolysis
body’s own enzymes act on itself, breaking down cells & tissues
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