Daniel:Notebook/ComboLock/2016-10-6: Difference between revisions

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(Created page with "=C Probe Positive Control Test (Started Yesterday)= Back to Calendar ==Protocol== <ol start="2"> <li>C...")
 
>Djacobse
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File:|qPCR curve
File:|qPCR curve
File:|Gel image
File:2016-10-06-PCCTest1-AmpFAmpR.png|Gel image
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Revision as of 23:12, 6 October 2016

C Probe Positive Control Test (Started Yesterday)

Back to Calendar

Protocol

  1. Circularization
    1. Heat inactivate enzyme by incubating for 2 minutes at 94C
  2. Exonuclease Digestion
    1. Prepare exonuclease I/III mix by mixing 20 uL exonuclease I (20 units/μL) and 4 uL exonuclease III (100 units/μL) in 1:1 ratio
    2. Add 2 μL of exonuclease I/III mix to reaction
    3. Mix the reaction by swirling pipette around the well 5 times
    4. Incubate reaction at 37 ºC for 2 hours
    5. Heat inactivate enzyme by incubating at 94C for 5 minutes
  3. qPCR
    1. Set up reaction according to table below
    2. Sample Molecule Count Lane AmpR Index Sample Vol (uL) 2X Kapa SYBR qPCR MM 100 uM AmpF 6.4 10 uM AmpR6.3-IndXX H2O Total Volume (uL)
      Sample1 1.00E+10 A1 24 2 25 0.5 5 17.5 50
      Sample2 1.00E+10 B1 25 2 25 0.5 5 17.5 50
      Sample3 1.00E+10 C1 26 2 25 0.5 5 17.5 50
    3. Make master mixes according to following recipes
      1. 54.25 uL nfH2O
      2. 77.5 uL SYBR Fast
      3. 1.55 uL AmpF
    4. Add 43 uL master mix to each well
    5. qPCR Cycles
      1. 95C 3 min
      2. 95C 3 sec
      3. 55C 30 sec
      4. 72C 20 sec
      5. plate read
      6. goto b x24
      7. 72C 2 min
      8. 16C hold
  4. TBE Gel
    1. Mix 40 uL TBE, 10 uL 6x loading dye
    2. Aliquot 10 uL per sample/ladder lane onto parafilm
    3. Add 2 uL of sample or ladder to correct drop
    4. Load 10 uL in to well
    5. Run gel for 22 minutes at 250V
    6. Open gel and stain with 3 uL SYBR Gold for 3 minutes
    7. Rinse gel and image in gel doc

Results