21.1 Dna Profiling Flashcards
What are exons
Dna that codes for proteins
What are introns
Non coding regions of dna
What is satellite dna
Short sequences of dna that are repeated many times
What is dna profiling
Producing an image of the patterns in the dna of an individual
What is the first stage of producing a dna profile
Extract the dna from a tissue sample
By using polymerase chain reaction
What do you do after you extract the dna using polymerase chain reaction in dna profiling
Digest the sample
Strands of dna are cut into small fragments using restriction endonucleases
They cut at specific restriction sites
What do restriction endonucleases do
Make 2 cuts at specific restriction sites once through each strand of the dna double helix
What happens after you digest the sample
You separate the dna fragments via electrophoresis
What is electrophoresis
At technique that utilises the way charger particles move through a gel medium under the influence of an electric current
It’s immersed into alkali to spectate the double strands into single strands and these are transferred onto a membrane for southern blotting
What happens after you spreads dna fragments in dna profiling
Hybridisation
Radioactive or fluorescent dna probes are now added in excess to dna fragments
The probes identify the microsatellite regions that are more varied than larger microsatellite regions
What are dna probes and what do they do
Are short dna or rna sequences complementary to a known DNA sequence
They bind to complementary strands of dna under particular conditions
What is the final step of dna profiling
The dna fragments give a pattern of bars which is the dna profile and it’s unique to every individual
What’s the difference between radioactive labels and flourescent labels added to dna probes
If Fluorescent labels are added the meme fans is placed under UV light so the fluorescent tags glow
If radioactive labels were added X-ray images are taken
What is polymerase chain reaction
Replicates dna and allows scientists to produce a lot of dna from the tiniest original sample
What is teh first stage of pcr
Separate the strand
Temperature in pcr machine is 90-95 for 30 seconds
This denatures the dna by breaking the hydrogen bonds holding the dna strands together