Noi/NOTES/2011-10-6: Difference between revisions
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'''Program'''<br> | '''Program'''<br> | ||
95C 30sec -> (95C 3sec -> 48C 30sec-> 60C 20sec) x 3 -> (95C 3sec -> 55C 30sec-> 60C 20sec) x 13 -> 60C 2min -> 15C hold | 95C 30sec -> (95C 3sec -> 48C 30sec-> 60C 20sec) x 3 -> (95C 3sec -> 55C 30sec-> 60C 20sec) x 13 -> 60C 2min -> 15C hold | ||
* Primer info. | |||
** eMIP_CA1_F: TGCCT'''AGGACCGGATCAACT''' (TGCCT overhang) | |||
** eMIP_CA1_R: GAGCT'''TCGGTTCACGCAATG''' (GAGCT overhang) | |||
* Note: | * Note: | ||
** The first three cycles, Tm of each primer was calculated without 5 nt overhang, the the Tm was increase based on the Tm of the whole primer length | ** The first three cycles, Tm of each primer was calculated without 5 nt overhang, the the Tm was increase based on the Tm of the whole primer length | ||
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* Purified with Qaiquick column and elute with EB buffer volume 50ul each | * Purified with Qaiquick column and elute with EB buffer volume 50ul each | ||
* Measure DNA conc. with Nanodrop and adjust conc. to 10nM for using as the template for the future amplification | * Measure DNA conc. with Nanodrop and adjust conc. to 10nM for using as the template for the future amplification | ||
* Perform production PCR | * Perform production PCR | ||
== Production PCR == | == Production PCR == | ||
{| {{table}} | {| {{table}} |
Revision as of 10:45, 7 October 2011
Plan of probe (from LC Bioscience) production
- Follow the protocol: [1] and standard protocol using to make DMR330k probe set
- After receiving the probes, resuspend with H2O to the concemtration 20 nM
- perform expansion PCR to amplify the probe as the template
Expansion PCR
Components | Volume (ul) | Final conc. |
20nM LC Sciences Oligoes | 2.00 | 0.2nM |
eMIP_CA1_F (100uM) | 0.80 | 400nM |
eMIP_CA1_F (100uM) | 0.80 | 400nM |
2x Kapa SYBG MM | 100.00 | 1x |
H2O | 96.40 | |
Total | 200.00 |
Program
95C 30sec -> (95C 3sec -> 48C 30sec-> 60C 20sec) x 3 -> (95C 3sec -> 55C 30sec-> 60C 20sec) x 13 -> 60C 2min -> 15C hold
- Primer info.
- eMIP_CA1_F: TGCCTAGGACCGGATCAACT (TGCCT overhang)
- eMIP_CA1_R: GAGCTTCGGTTCACGCAATG (GAGCT overhang)
- Note:
- The first three cycles, Tm of each primer was calculated without 5 nt overhang, the the Tm was increase based on the Tm of the whole primer length
- The number of cycles will be monitored
- Purified with Qaiquick column and elute with EB buffer volume 50ul each
- Measure DNA conc. with Nanodrop and adjust conc. to 10nM for using as the template for the future amplification
- Perform production PCR
Production PCR
Components | 1 rxn | 32x rxn mix |
1st round amplicon (10nM) | 0.20 | 6.40 |
eMIP_CA1_F (100uM) | 0.40 | 12.80 |
eMIP_CA1_F (100uM) | 0.40 | 12.80 |
2x Kapa SYBG MM | 50.00 | 1600.00 |
H2O | 49.00 | 1568.00 |
Total | 100.00 | 3200.00 |
Program
95C 30sec -> (95C 3sec -> 55C 30sec-> 60C 20sec) x 16 -> 60C 2min -> 15C hold
- The number of cycles will be monitored to prevent overamplification