gel electrophoresis
DNA identification
1. Isolate the DNA in a sample, and if needed, make copies: 2. Cut the DNA into shorter fragments that contain known VNTR areas: 3. Sort the DNA by size: 4. Compare the size fragments in the unknown sample of DNA to those of known samples of DNA.
how big is DNA molecules
3 meters
what helps to make the bands of DNA visible
A chemical in the gel that the DNA passes through binds to the DNA and is visible under UV light.
why are they moving through the gel?
As the DNA is negatively charged it will move from the well towards the bottom of the gel which is positive
how is a DNA fingerprint used to identify unknown DNA samples or used in making medical diagnosis
It takes fragments are used to identify a person's DNA fingerprint. and used in medicine to diagnose hereditary genes
what is different in the movement of the short vs longer molecules in a gel electrophoresis
Shorter ones will move faster through the gel than longer ones
How are DNA molecules sorted by a gel?
The gel acts like a sieve, separating different DNA molecules according to their size, as smaller DNA molecules will be able to move through the gel quicker than larger molecules.
running buffer
What allows a current to travel through the gel tray
how do molecules move through the gel in gel electrophresis process
an electric current passes DNA samples through a gel
Why is it called a DNA fingerprint?
because it is very unlikely that any two people would have exactly the same DNA information, in the same way that it is very unlikely that any two people would have exactly the same physical fingerprint.
casting tray
casting tray is to make sure the gel is not contaminated
comb
comb is to make the holes to put the dna in To ensure there's a place to put the DNA in the gel, a comb is placed in the agarose liquid before it cools. Each tooth in the comb will become a hole, or 'well,' in the solidified agarose gel.
electricity
electricity is so that each substance will seperate
gel box
gell box is to make sure the electricity goes directly to the gel
bumper
placed at the end of the casting tray and removed when the agarose gel hardens
role of restriction enzymes in the gel electrophoresis process
recognizes and cuts, or digests, only one particular sequence of nucleotide bases in DNA, and it cuts this sequence in the same way each time. Typically restriction enzymes used in cloning recognize four-,six, or eight base sequences. Hundreds of restriction enzymes are known, each producing DNA fragments with characteristic ends. Restriction enzymes can cut blunt ends (cuts directly opposite each other) or sticky ends (staggered cuts)
restriction enzymes
restiriction enzimes were to cut the DNA at a certain point
loading and staining dyes
staining dies were to show the process and to show each different type
well
the well is so that the electricity can reach the gel,
how do restriction enzymes function
they leave overhanging "sticky" ends recognizes a specific sequence of DNA and cuts it in a specific way
3 scenarios where a DNA fingerprint is useful
to convict someone of murder. to identify an unknown body. to determine is you carry a hereditary gene that can cause an illness
agarose gel
used to separate fragments of DNA based on size. The hot agarose liquid is poured into a casting tray. Once the mixture cools, a thin agarose brick will form.
Micropipettes
were to insert the dna into the wells.
five cell types that could be used as a source of DNA for a fingerprint?
white blood cells from blood, hair, skin, saliva, semen