Matt:LabNotes/2016-6-7

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Revision as of 21:38, 10 June 2016 by >Mzcai (→‎Lambda Exo)
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TB12k_Apr2016 V4 Probe Preparation

Production PCR

  • Make 2X V4 master mix
Components Volume (1X) Volume (50X)
First round amplicon TB12k_Apr2016_V4 (10nM) 0.2 10
2X KAPA SYBG MM 50 2500
AP1V4U (100uM) 0.4 20
AP2V4 (100uM) 0.4 20
H2O 49 2450
Total 100 5000

Program 98C 1min -> (98C 30sec -> 55C 45sec -> 72C 45sec) x 14 -> 72C 2min -> 4C hold

  • No curve because 100ul reaction volume only works in Biorad PCR machines

EtOH Precipitation

  • 8 15-ml tubes (with 24 wells (3 strips) of PCR product each) for
    • 1,200ul PCR product
    • 3000ul 100% EtOH
    • 4ul GlycoBlue
    • 120ul 3M NaOAc pH 5.2-5.5
  • Vortexed and put in -80C for overnight
  • Centrifuged at 3000rpm at 4C for 30 min
  • Discarded supernatant and added 800ul of cold 80% EtOH
  • Transferred DNA pellet (with 1ml pipette tip) to 8 1.5mL tubes
  • Centrifuged 1.5ml tubes at 14,000rpm for 5 min at 4C
  • Discarded supernatant and air-dried for 5 min in hood
  • Resuspended DNA with 100ul H2O

Qia Column Purification

  • 8 columns elute 50ul each
  • Nanodrop: 313.6 ng/uL x 400uL = 125.44ug

Lambda Exo

  • Divide into 8 pcr tubes of 100ul (ideally should be <10ug each)
Components Volume
Amplicon 50
10X Lambda Exo Buffer 10
Lambda Exonuclease 10
H2O 30
Total 100
  • Incubated at 37C for 2hr (normally 1hr)
  • Purified with 8 Zymo ssDNA/RNA columns
    • Dropped one column so only 7
  • Eluted with 40ul each
  • Recombined and measured ssDNA with Nanodrop:
    • 118.7ng/ul x 280ul = 33.24ug