Team:UNC Chapel Hill/26 July 2009

From 2009.igem.org

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Spectrophotometer results:
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[[Team:UNC_Chapel_Hill/Notebook|Back]]
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*A1: -11.8 ng/uL
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*Miniprepped everything that was cultured overnight except for pSB1A3, which is not supposed to be red (WTF).  Recultured pSB1A3 with a non-red colony.
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*A2: 3.5 ng/uL
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*Made a positive control to test to see if the KAN plates were good.
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re-blanked here
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*Tested the Optical Density of the solutions.  Spectrophotometer results:
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*A3: -1.2
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**A1: -11.8 ng/uL
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*A4: -7.1
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**A2: 3.5 ng/uL
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*A5: -4.2
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***re-blanked here
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*A6: -6.9
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**A3: -1.2 ng/uL
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blanked with different water here
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**A4: -7.1 ng/uL
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*A7: -6.9
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**A5: -4.2 ng/uL
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**A6: -6.9 ng/uL
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Something is definitely wrong.  Either with the miniprepping or the spectrophotometery.
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***blanked with different water here
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**A7: -6.9 ng/uL
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*Something is definitely wrong.  Either with the miniprepping or the spectrophotometery.

Latest revision as of 19:54, 27 July 2009

Back

  • Miniprepped everything that was cultured overnight except for pSB1A3, which is not supposed to be red (WTF). Recultured pSB1A3 with a non-red colony.
  • Made a positive control to test to see if the KAN plates were good.
  • Tested the Optical Density of the solutions. Spectrophotometer results:
    • A1: -11.8 ng/uL
    • A2: 3.5 ng/uL
      • re-blanked here
    • A3: -1.2 ng/uL
    • A4: -7.1 ng/uL
    • A5: -4.2 ng/uL
    • A6: -6.9 ng/uL
      • blanked with different water here
    • A7: -6.9 ng/uL
  • Something is definitely wrong. Either with the miniprepping or the spectrophotometery.