Test Your Own Genes

Isolate Your DNA
1. Amplify Your DNA By PCR
  1. Digest PCR Products With Restriction Enzyme HaeIII
    1. Analyze PCR Products By Gel Electrophoresis
      1. Determine Your PCR Genotype and Phenotype
        Results of gel electrophoresis
        Indicate heterozygous and homozygous dominant genotypes
        Heterozygous carriers have one dominant and one recessive allele resulting in three bands because HaeIII cuts twice on the dominant allele and none on the recessive allele. Though HaeIII cuts twice on the dominant allele only two bands are shown for both alleles because they are the same base pair length and therefore occupy the same spot not the gel. Homozygous recessive individuals will have a singular band because HaeIII didn't cut anywhere.
        Goal: Analyze electrophoresis results then use PTC paper to determine if the gel results match our phenotype
      2. Place the gel in the electrophoresis chamber and add buffer
        Lane 1: 20 microliters of DNA marker
        Lane 2: 10 micrometers of student 1 undigested DNA
        Lane 3: 15 microliters of student 1 digested DNA
        Lane 4: 10 micrometers of student 2 undigested DNA
        Lane 5: 15 microliters of student 2 digested DNA
        Let the gel run for at least 30 minutes then view with a white light box
      3. Goal: Run and stainless then view the results using a white light box
    2. Label two tubes digested and undigested
      1. Transfer 15 microliters of PCR product into the digested tube and transfer the remaining amount into the undigested tube
        Transfer the Haelll enzyme directly into the digested tube and pipet up and down to mix
        HaeIII recognizes the sequence GGCC and cuts bluntly - perfect for analysis because the DNA fragments don't stick back together
        Tap the bottom of the tube on a lab bench to mix and pool the reagents
        Transfer the digested sample into a .2 ml tube
        incubate at 37 degrees for one hour
    3. Goal: Identify SNPs or base pair differences in the amplifies sequence of TAS2R38
  2. Obtain a PCR tube with the ready-to-go PCR bead and label with your initials
    1. Add loading dye, place the tube on ice, allow the bead to dissolve
      1. The dye will turn purple as the bead dissolves
        Dye allows use to see the cheek cells
      2. Place the PCR tube in a thermal cycler
        Store the amplified DNA on ice
  3. Goal: Use PCR to make multiple copies of TAS2R38 gene for analysis
2. Label a 1.5 microcentrifuge tube with your intiials
  1. Pour all of the saline solution into your mouth and swish for thirty seconds
    1. Spit the liquid into a paper cup
      1. Swirl the cup and mix the cheek cells then transfer to the labeled microcentrifuge
        Centrifuge
        Concentrates all the DNA from the cheek cells at the bottom of the tube
        Pour off the supernatant
        Because it no longer contains any cheek DNA
        Pipet up and down to resuspend the pellet
        It spreads the DNA
        Add chelex to protect the cheek cells from heat
        Heat the tube
        Releases the DNA from the nucleus
        Cell lysis
        When cool, shake the tube
        Centrifuge
        Transfer supernatant to a labeled 1.5 tube
        The supernatant now contains the DNA from the cheek cells and the pellet contains debris
3. Goal: Extract a sample of cheek cells to start your PCR reaction
Goal: Use the DNA from cheek cells to find an individual's genotype for PTC and compare these results to the phenotype

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Test Your Own Genes

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Zusammenfassung der Ressource

Medienanhänge

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	Erstellt von Tashelle Davis vor mehr als 8 Jahre