Matt:LabNotes/2017-6-7: Difference between revisions
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*[[Matt:LabNotes/2017-5-15|Third try confirmed second try]] | *[[Matt:LabNotes/2017-5-15|Third try confirmed second try]] | ||
*[[Matt:LabNotes/2017-5-19|Fourth try had unexpected non-continous trend]] | *[[Matt:LabNotes/2017-5-19|Fourth try had unexpected non-continous trend]] | ||
*[[Matt:LabNotes/2017-5- | *[[Matt:LabNotes/2017-5-22|Fifth try]] | ||
*Repeat Fifth Try with 95C 3min denature before hybridization | *Repeat Fifth Try with 95C 3min denature before hybridization | ||
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#Incubate at 94C for 5min | #Incubate at 94C for 5min | ||
#Purify 20ul with Zymo ssDNA purification kit, elute 20ul | #Purify 20ul with Zymo ssDNA purification kit, elute 20ul | ||
#Dilute 5ul in 45ul H2O (10x dilution) | |||
#qPCR all 16 samples with triplicates | #qPCR all 16 samples with triplicates | ||
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Program | Program | ||
98C 1min -> (98C 10s -> 52C 20s -> 72C 20s)x26 -> 72C 3min | 98C 1min -> (98C 10s -> 52C 20s -> 72C 20s)x26 -> 72C 3min | ||
===Results=== | ===Results=== | ||
[[Media: | [[Media:20170610_qPCR_PPcapture_SplintRformamide.xlsx|raw data here]]<br> | ||
[[File: | [[File:20170610_qPCR_PPcapture_SplintRformamide_ScatterPlot.PNG|450px]] | ||
==Conclusion== | |||
*Finally got a linear trend that makes sense for increasing formamide | |||
*5% formamide or 10% DMF is best |
Latest revision as of 22:42, 12 June 2017
Sixth Try: in tube SplintR Test with formamide[edit]
- First try showed SplintR with 10% formamide had the best sensitivity and specificity of the conditions tried
- Second try had unexpected trend with increasing formamide led to increased sensitivity
- Third try confirmed second try
- Fourth try had unexpected non-continous trend
- Fifth try
- Repeat Fifth Try with 95C 3min denature before hybridization
Test Conditions[edit]
- Standard: SplintR only
- SplintR + 5% formamide
- SplintR + 10% formamide
- SplintR + 15% formamide
- SplintR + 1M Betaine
- SplintR + 10% dimethylformamide
- SplintR + 5% DMSO
- Positive Control: Ampligase
- For each test conditions have
- one sample with ALL padlock probes and template
- Should see amplification
- one sample with all padlock probes with NO MALAT1 template
- Should not see amplification
- one sample with ALL padlock probes and template
Padlock Probes and Template[edit]
- ppCUX2
- ppBCL11B
- ppRELN_1
- ppGFAP
- ppMALAT1
- /5Phos/TTTCTGCCTTTACTTATCAATTCCTTCAGCTTCCCGATATCCGACGGTCTACTTCGTCGCGTCAGACCAAATGGAGGTATGACATATAATCT
- Template for ppMALAT1: MALAT1_template
- /5AmMC6/GAATTGATAAGTAAAGGCAGAAA AGATTATATGTCATACCTCCAT
Protocol[edit]
Sample # | Condition | 30nM PP + Template | 10X Buffer | Formamide | DMF | Betaine | DMSO | H2O | Total |
1 | SplintR | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 0 | 0 | 0 | 0 | 22.5 or 21.6 | 30 |
2 | SplintR + 5% formamide | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 1.5 | 0 | 0 | 0 | 21 or 20.1 | 30 |
3 | SplintR + 10% formamide | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 3 | 0 | 0 | 0 | 19.5 or 18.6 | 30 |
4 | SplintR + 15% formamide | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 4.5 | 0 | 0 | 0 | 18 or 17.1 | 30 |
5 | SplintR + 10% DMF | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 0 | 3 | 0 | 0 | 19.5 or 18.6 | 30 |
6 | SplintR + 1M Betaine | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 0 | 0 | 6 | 0 | 16.5 or 15.6 | 30 |
7 | SplintR + 5% DMSO | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 0 | 0 | 0 | 1.5 | 21 or 20.1 | 30 |
8 | Ampligase | 4.5 or 5.4 (0.9ul of each 1uM oligo) | 3 | 0 | 0 | 0 | 0 | 22.5 or 21.6 | 30 |
- Combine padlock probes and template in 1X Ligase buffer and possibly additives
- Add mineral oil on top
- Incubate at 95C for 3min
- Incubate at 55C for 18hr
- To sample 8 add 3ul Ampligase Mix and incubate at 55C for 1hr30min
- Ampligase Mix: 1ul Ampligase + 1ul 10X Ampligase Buffer + 8ul H2O
- Move samples 1-7 to 37C
- Move one tube at a time and add enzyme after holding tube between fingers for 5 sec
- Add 3ul SplintR Mix and incubate 15min
- SplintR Mix: 27ul SplintR + 4.5ul 10X SplintR Buffer + 13.5ul H2O
- Incubate at 94C for 5min
- Put all samples on ice and add 2ul Exo I/III mix
- Incubate at 37C for 1hr
- Incubate at 94C for 5min
- Purify 20ul with Zymo ssDNA purification kit, elute 20ul
- Dilute 5ul in 45ul H2O (10x dilution)
- qPCR all 16 samples with triplicates
Components | 1X Volume | 48X Volume |
Captured template | 1 | 0 |
10uM ISB_CA_AF | 0.4 | 19.2 |
10uM ISB_CA_AR.T2 | 0.4 | 19.2 |
2X KAPA SYBG MM | 12.5 | 600 |
H2O | 10.7 | 513.6 |
Total | 25 | 1,152 |
- Aliquot 24ul from 48X master mix and add 1ul captured template
Program 98C 1min -> (98C 10s -> 52C 20s -> 72C 20s)x26 -> 72C 3min
Results[edit]
raw data here
File:20170610 qPCR PPcapture SplintRformamide ScatterPlot.PNG
Conclusion[edit]
- Finally got a linear trend that makes sense for increasing formamide
- 5% formamide or 10% DMF is best