Noi/NOTES/2013-5-24: Difference between revisions

From ZhangLabWiki
Jump to navigation Jump to search
>Noi
mNo edit summary
>Noi
mNo edit summary
Line 105: Line 105:


* PAGE analysis to verify the PCR products by loading 5 ul of PCR product without bead purification (1/10 of total volume)
* PAGE analysis to verify the PCR products by loading 5 ul of PCR product without bead purification (1/10 of total volume)
  [[File:ZhangLab_2 2013-05-24 15hr 41min_1-8.jpg| 275px]] [[File:ZhangLab_2 2013-05-24 15hr 43min_9-16.jpg| 275px]]  [[File:ZhangLab_2 2013-05-24 15hr 46min_17-24_e.jpg| 275px]]
  [[File:ZhangLab_2 2013-05-24 15hr 41min_1-8.jpg| 320px]] [[File:ZhangLab_2 2013-05-24 15hr 43min_9-16.jpg| 325px]]  [[File:ZhangLab_2 2013-05-24 15hr 46min_17-24_e.jpg| 325px]]
* All samples worked as expected since Eric did qPCR to verify the yield of MDA.
* The average size of libraries looked smaller than the ones on May22

Revision as of 00:23, 25 May 2013

Adaptor ligation of CoRE fragmented DNA from Eric (May 23, 2013 experiment)

  • Got 24 samples from Eric for ligation using NEBNext adaptor.
  • MDA and CoRE fragmentation were performed by Eric and documented on Eric's note on May23, 2013: [[1]]
  • All procedures of adaptor ligation and amplification were the same as experiment on My22, 2013

Adaptor ligation

Reaction set up

Components Volume (ul)
Fragmented DNA 6.00
1.5uM NEBNext adaptor 1.67
Ligation reaction mix 42.33
Total 50.00

NEBNext adaptor preparation

  • I diluted a new batch of adaptor by diluting 15uM adaptor to 1.5uM (mix 20ul of 15uM NEBNext adaptor with 180ul H2O) and aliquoted 25ul into 8-striptubes and saved at -20C after used.

Ligation reaction mix

Ligation reaction mix 1x rxn 24x rxn mix
2X KAPA Rapid Ligation Buffer 25.00 600.00
KAPA Rapid T4 DNA Ligase 2.00 48.00
H2O 15.33 367.92
Total 42.33 1,015.92
  • Aliquot 42.33 ul of ligation reaction mix to each tube containing 6ul of fragmented DNA
  • Add 1.67ul of 1.5uM NebNext loob adaptor. Mix well by pipetting 15-20 times and quick spin.
  • 25C for 10min
  • Add 2ul USER. Mix well by pipetting 15-20 times and quick spin. 37C for 15min
    • For the library prep using NEBNext® DNA Library and this loop adaptor, they used 3ul USER in total volume 50ul or 83.5ul, 37 C for 15 min. I used a little less

Bead purification

  • 50ul AmPure beads mix by pipetting 10 times
  • Wait 10min
  • Sit on magnetic stand 5min
  • Wash twice with freshly prepared 80% EtOH (after adding 80% EtOH, I wait for 30sec before pipette up and down few times and discard spnt)
    • I wash with 160ul of 80% EtOH since I used low profile tube.
  • Dry the beads for 3 min
  • Eluted with 20ul H2O (resuspend and wait for 2min, used all for PCR)

Amplification

Components 1x rxn 25 rxn mix
adapter ligated DNA 20.00 0.00
PCR_F (NEB, 10uM) 1.00 25.00
NEBNext.IndX (NEB, 10uM) 1.00 0.00
2X KAPA SYBR MM 25.00 625.00
H2O 3.00 75.00
Total volume 50.00 725.00
  • Aliquot 29ul, add 1ul of NEBNext Indx, 20ul of adapter ligated DNA
Samples Indx Samples Indx
#1 NEBNext Index1 #13 NEBNext Index1
#2 NEBNext Index2 #14 NEBNext Index2
#3 NEBNext Index3 #15 NEBNext Index3
#4 NEBNext Index4 #16 NEBNext Index4
#5 NEBNext Index5 #17 NEBNext Index5
#6 NEBNext Index6 #18 NEBNext Index6
#7 NEBNext Index7 #19 NEBNext Index7
#8 NEBNext Index8 #20 NEBNext Index8
#9 NEBNext Index9 #21 NEBNext Index9
#10 NEBNext Index10 #22 NEBNext Index10
#11 NEBNext Index11 #23 NEBNext Index11
#12 NEBNext Index12 #24 NEBNext Index12
Program (Eppendorf Realplex)

98C - 30s, (98C - 10s, 65C - 30s, 72C - 45s)x15, 72C - 2min, hold at 15C

I stopped the reaction at 11 cycles
  • PAGE analysis to verify the PCR products by loading 5 ul of PCR product without bead purification (1/10 of total volume)
File:ZhangLab 2 2013-05-24 15hr 41min 1-8.jpg File:ZhangLab 2 2013-05-24 15hr 43min 9-16.jpg  File:ZhangLab 2 2013-05-24 15hr 46min 17-24 e.jpg
  • All samples worked as expected since Eric did qPCR to verify the yield of MDA.
  • The average size of libraries looked smaller than the ones on May22