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PCR & DNA Profiling
PCR
| Question | Answer |
|---|---|
| What does PCR stand for ? | Polymerase Chain Reaction |
| What is added to the DNA sample during PCR ? | DNA poymerase, DNA primer (florescent), nucleotides |
| What is the temperature used to break the DNA into 2 strands ? | 95 degrees Celsius |
| What is the primer used for ? | The primer bonds to the DNA to form a starting point for DNA synthesis |
| What is a restriction enzyme ? | An enzyme used to cut the STR |
| which end of the DNA strand do the primers bond to ? | The 3 end |
| Where does the DNA polymerase come from for PCR ? | Bacteria from hot water geysers |
| Define STR | Short tandem repeat |
| why can't you use human polymerase during PCR ? | The Enzyme will be denatured |
| What is PCR used for ? | Amplifying DNA |
| What is another name for DNA profiling ? | DNA fingerprinting, Gel electrophoresis |
| what is the name of the jelly where the DNA samples are put into ? | Agarose jelly |
| What is the name of the holes made in the agarose for the DNA samples ? | Wells |
| What is the buffer liquid used for in gel electrophoresis ? | To prevent any change in pH |
| What charge does DNA have ? | Negative |
| When DNA probs are added top the DNA how will you be able to see them ? | By adding a florescent or radioactive substance to the DNA probs |
| Which DNA strands move fastest ? | Short strands with the smallest number of base pairs |
| When do the DNA strands separate ? | when the DNA is attached to the nylon paper |