Gel electrophoresis
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Transcript of Gel electrophoresis
JESSICA PARTIN
GEL ELECTROPHORESIS
o A method used in biology to separate DNA strands to create a DNA fingerprinto Separates the DNA by size lengths o Uses an electric current to separate DNA
WHAT IS GEL ELECTROPHORESIS?
FINAL PRODUCT
Extract DNA from organism and place
in tubes
STEP 1
Polymerase Chain Reaction
STEP 2
(this is before the process of gel electrophoresis)
*this is used to make millions of copies of the DNA
PCR STEPS Denature= rips apart DNA
Lasts about 1 minute At about 94˚F
Annealing= starts the coping DNALasts about 45 secondsAt about 54˚F
Extension= finishes copying DNALasts about 3-5 minutesAt about 72˚F
Repeat 30-40 times
STEP 3
Place restriction enzymes in DNA
(This cuts the DNA into different lengths)
STEP 4
Dye the DNA and place it into gel
(the gel is usually agarose gel)
STEP 5
Run electrical current though gel
(negative to positive)
STEP 6
Place in stain, then under UV lighting.
The smallest DNA fragments move the fastest and farthest
USES Evidence in criminal cases To determine paternity To diagnose genetic diseases Help to determine kinship in animals
Compare similarities and differences between species
PROS VS. CONSSmall amount of
starting material (DNA) needed
DNA can be detected regardless of size
of DNA
Hazardous material
Expensive
Very time consuming
*The Macgyver Project used gel electrophoresis
FUNNIES;)
GO TO THIS WEBSITE:
learn.genetics.utah.edu/content/labs/gel
This is a very helpful interactive site that I got most of my information from. If you would like to know more about gel electrophoresis in more detail, I highly suggest this site!