Kun:LabNotes/CpgSeq/2007-12-11: Difference between revisions
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(New page: ==Exp.1 Repeat the PCR experiment on the circularized reactions using Hd48MIP1,2,5 primers with a touchdown protocol== Template: 1ul (1:100 dilution of bifulfite converted ...) |
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Total number of reactions: 4 MIP reactions x 3 primer pairs + 2 control x 3 primer pairs = 18 | Total number of reactions: 4 MIP reactions x 3 primer pairs + 2 control x 3 primer pairs = 18 | ||
95C 15min -> 8 cycles of (94C 30sec -> 60C 30sec (-0.5C per cycle) -> 72C 30 sec) -> 27 cycles of (94C 30sec -> 56C 30sec -> 72C 30 sec) -> 72C 3min -> 15C hold. | 95C 15min -> 8 cycles of (94C 30sec -> 60C 30sec (-0.5C per cycle) -> 72C 30 sec) -> 27 cycles of (94C 30sec -> 56C 30sec -> 72C 30 sec) -> 72C 3min -> 15C hold. | ||
==Exp.2 Perform another round of capturing reaction at 60C== | |||
#dsDNA synthesis: | |||
DNA 20ul | |||
10x NEBbuffer2 3ul | |||
10mM dNTP 1.5ul | |||
100uM N6 3ul | |||
94C 3min -> snap on ice for >1min -> add 2ul 10U/ul DNA Pol I -> 16C 15min -> 37C 30min -> 75C 10min. | |||
Purify with MinElute columns, eluted with 22ul ddH2O. Measure concentration. |
Revision as of 22:40, 11 December 2007
Exp.1 Repeat the PCR experiment on the circularized reactions using Hd48MIP1,2,5 primers with a touchdown protocol
Template: 1ul (1:100 dilution of bifulfite converted gDNAs) 10X buffer: 2.5ul 10mM dNTP: 0.5ul 10uM Primer pair 0.75ul 50X SYBR I 0.2ul AmpliTaq Gold 0.25ul H2O 20ul
Total number of reactions: 4 MIP reactions x 3 primer pairs + 2 control x 3 primer pairs = 18 95C 15min -> 8 cycles of (94C 30sec -> 60C 30sec (-0.5C per cycle) -> 72C 30 sec) -> 27 cycles of (94C 30sec -> 56C 30sec -> 72C 30 sec) -> 72C 3min -> 15C hold.
Exp.2 Perform another round of capturing reaction at 60C
- dsDNA synthesis:
DNA 20ul 10x NEBbuffer2 3ul 10mM dNTP 1.5ul 100uM N6 3ul
94C 3min -> snap on ice for >1min -> add 2ul 10U/ul DNA Pol I -> 16C 15min -> 37C 30min -> 75C 10min. Purify with MinElute columns, eluted with 22ul ddH2O. Measure concentration.