Introduction:
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001000000110001101100001011011100010000001110010
011001010110000101100100001000000111010001101000
011010010111001100100000011110010110111101110101
001000000110000101110010011001010010000001100001
001000000110001001101111011100110111001100100000
011000010110111001100100001000000111001101101000
011011110111010101101100011001000010000001100111
011010010111011001100101001000000110110101100101
001000000110000101101110001000000100000100100000
011011110110111000100000011011010111100100100000
011011000110000101100010001011100010000001000110
011001010110010001100100011001010111001001110011
011011110110111000101100001000000100100100100000
011000010111001101110011011101010110110101100101
001000000111010001101000011010010111001100100000
011010010111001100100000011110010110111101110101
001000000111001001100101011000010110010001101001
011011100110011100100000011101000110100001101001
011100110010000001110011011011110010000001111001
011011110111010100100000011000110110000101101110
001000000110000101110000011100000111001001100101
011000110110100101100001011101000110010100100000
011101000110100001100101001000000110010101110000
011010010110001101101110011001010111001101110011
001000000110111101100110001000000110110101111001
001000000110001001101100011000010110001000101110
The genome is our hereditary code made up of DNA. Biotechnology uses this knowledge to manipulate organisms. Polymerase Chain Reaction is used to amplify a specific sequence of DNA.
Tuesday, March 15, 2011
Tuesday, March 1, 2011
P glo
The goal of this lab is to make bacteria glow. We will be inserting the DNA for Green Florescent Protein (GFP) into the bacteria's DNA. This will be done by subjecting the bacteria to heat shock. Heat shock is a rapid change in temperature. The rapid change in temperature will cause the bacteria to absorb DNA mediately around it, thus absorbing the DNA with the GFP gene. To ensure that only the bacteria that absorbed the DNA survive, we will attach the coding for the GFP with the coding for ampicilin resistance. Then, after the bacteria has gone through heat shock and absorbed the DNA, the bacteria then will be subjected to ampicillin, therefore killing off all of the bacteria that did not absorb the DNA. The remaining ampicillin resistant bacteria should glow green if all went correctly.
Friday, January 28, 2011
Identifiying Devil Crops: The study of GMOs
Well, the problem here with the GMOs has been grounded in history for many years. Actually, only as many years as GMOs have existed, which is only about 24, since they mainly started in 1986. But, nonetheless, GMO's are genetically modified organisms. Scientists have deemed it necessary to tinker with God's almighty creations in order to protect crops from frost, or disease. They manipulate the genes of species in order to breed specific, beneficial traits. However, many sensible people object to gmos because their effect on humans are unknown.
Procedure:
Grind fruit with pestle. Label the tubes 1 through 6. Add the master mix. place the the mixture in the PCR tubes. Place the PCR tubes in the thermal cycler. Put loading dye in each one. Run each one through gel electrophoresis.
Results/Discussion:
Lane 1: Test Food 1 Plant Master Mix
Lane 2: Test Food 1 GMO Master Mix
Lane 3: Test Food 2 Plant Master Mix
Lane 4: Test Food 2 GMO Master Mix
Lane 5: GMO+ Plant Master Mix
Lane 6: GMO+ GMO Master Mix
Lane 7: Gel Marker
However, our results might be skewed for we mixed up lanes 1 and 3 making our results different from what was expected
Lane 7: PCR Molecular weight ruler.
Procedure:
Grind fruit with pestle. Label the tubes 1 through 6. Add the master mix. place the the mixture in the PCR tubes. Place the PCR tubes in the thermal cycler. Put loading dye in each one. Run each one through gel electrophoresis.
Results/Discussion:
Lane 1: Test Food 1 Plant Master Mix
Lane 2: Test Food 1 GMO Master Mix
Lane 3: Test Food 2 Plant Master Mix
Lane 4: Test Food 2 GMO Master Mix
Lane 5: GMO+ Plant Master Mix
Lane 6: GMO+ GMO Master Mix
Lane 7: Gel Marker
However, our results might be skewed for we mixed up lanes 1 and 3 making our results different from what was expected
Lane 7: PCR Molecular weight ruler.
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