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DNA profiling
PCR and DNA profiling
| Question | Answer |
|---|---|
| Name the temperatures that DNA is treated at in PCR | 95, 55 and 70 degrees celsius |
| What charge is DNA? | negative |
| Name the jelly used in gel electrophoresis | agarose |
| What does the distance the DNA has travelled, depend on? | the number of base pairs in DNA length |
| What does STR stand for? | Short tandem repeat/ satellites |
| non coding blocks | introns |
| coding blocks | exons |
| what do the DNA strands have to do in order for primers to attach in Southern blotting | DNA strands must separate |
| Why is PCR carried out? | To increase the quantity of DNA in the sample |
| another name for DNA fingerprinting | gel electrophoresis/ DNA profiling |
| why are DNA probes used in Southern blotting | to make the DNA show up |
| name the liquid in gel electrophoresis | buffer solution |
| name the types of DNA probe used | fluorescent/radioactive |
| what is used to cut DNA? | restriction enzymes |
| other than the DNA sample what is added in PCR? | DNA polymerase, DNA primers and nucleotides |
| where does the DNA polymerase come from? | taq amylase (bacteria) |
| name the scientist who developed the PCR method | Alec Jeffreys |
| why would you create a DNA profile? | crime, paternity, identification, research, food standards |
| what are short tandem repeats? | short DNA sequences that are found in introns |
| How many base pairs can form an STR? | 2-50 |
| How many times is the sequence in an STR repeated? | 5-100s |
| Is it possible for two people to have the same number of repeats? | YES! |
| where do restriction enzymes cut? | wherever on the DNA the scientist wishes them to be cut (either side of an STR) |
| in gel electrophoresis what are the holes called that the DNA is inserted into? | wells |
| At a particular loci would the number of STR repeats be the same on both chromosomes of a homologous pair? | No, it is likely that the number of repeats would be different on the paternal strand to the maternal strand |