AlanFung:LabNotes/CTCF/2011-6-7: Difference between revisions

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==Synthesize 2nd strand with N9 primer and klenow exo==
==Synthesize 2nd strand with N9 primer and klenow exo==
* Add 1 uL Klenow Polymerase(1U/ul) and
* Incubate for 10min at 30 C


==Perform standard tagmentation and PCR amplification with orange/blue primers==
==Perform standard tagmentation and PCR amplification with orange/blue primers==

Revision as of 23:49, 7 June 2011

qPCR with CHR8 primer using pfu Cx polymerase on bisulfite converted GM12878 gDNA

Protocol

Component amount per reaction
distilled water 35.6
10x pfuturbo cx reaction buffer 5
dNTPs(10mM each DNTP) 1
DNA template 1
CHR8 F primer 3.3uM 3
CHR8 R primer 3.3um 3
sybr green 50x 0.4
pfuturbo cx hotstart dna polymerase 2.5U/ul 1
total reaction volume 50
    • Perform Manufacturer protocol for PfuTurbo Cx Hotstart DNA Polymerase
95C 2m
95C 30s
52C 30s
72C 2m
Plate Read
Go to step 2 repeat for 29 times
72C 10m
15C hold

Results

File:060611 CHR8 pfuCx.jpg

  • Amplification failed with Pfu cx polymerase

Perform bisulfite conversion on 6ng, 1.2ng, and 600pg of gDNA using Zymo’s direct kit

Tube Amount Volume per Reaction Tube Concentration H2O
A 6ng 1.2 5ng/ul 18.8
B 1.2ng 6.82 176g/ul 13.18
C 600pg 3.41 176g/ul 16.59
D Blank 0 N/A 20
  • Warm CT conversion Reagent (prepared on 6/6/11) up to 37C and vortex in 37C incubator
  • Add 130ul CT Conversion Reagent to each tube

Synthesize 2nd strand with N9 primer and klenow exo

  • Add 1 uL Klenow Polymerase(1U/ul) and
  • Incubate for 10min at 30 C

Perform standard tagmentation and PCR amplification with orange/blue primers