Chris:LabNotes/FateMapping/Calendar/2014/2014-8-18: Difference between revisions
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>Cjwei (Created page with "=Target capture with padlock probes (designed 5/12) test with Rui's probes as control= ==Background== *So far, I have not gotten a good probe capture result yet (as the result...") |
>Cjwei No edit summary |
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12 0ng(NTC, CW) 500:1 8.25 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization) | 12 0ng(NTC, CW) 500:1 8.25 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization) | ||
13 0ng(NTC, RL) 1000:1 0.32 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization) | 13 0ng(NTC, RL) 1000:1 0.32 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization) | ||
*Dilute my probe mix to | *Dilute my probe mix to 1ng probe/ul (will dilute probes produced on 7/10, which was ~14ul, ~60ng/ul) | ||
**Probe concentration is ~60ng/ul -> 1/ | **Probe concentration is ~60ng/ul -> 1/60d -> 1ul probe + 59ul water (save this for later so will not need to dilute so many times) | ||
*Dilute Rui's probe mix to 0.1ng/ul | *Dilute Rui's probe mix to 0.1ng/ul | ||
**Probe concentration is ~1ng/ul -> 1/10d -> 2ul probe + 18ul water | **Probe concentration is ~1ng/ul -> 1/10d -> 2ul probe + 18ul water | ||
*Dilute target human gDNA concentration to 10ng/ul | *Dilute target human gDNA concentration to 10ng/ul | ||
**gDNA concentration is ~110ng/ul -> 1/11d -> | **gDNA concentration is ~110ng/ul -> 1/11d -> 4ul gDNA + 40ul water | ||
*Final volume of probe and target to add to each rxn | *Final volume of probe and target to add to each rxn | ||
rxn Target (ul) Probe (ul) Water (ul) -> to get to 20ul total volume | rxn Target (ul) Probe (ul) Water (ul) -> to get to 20ul total volume | ||
1 | 1 10 8.25 (CW) 1.75 | ||
4 | 2 10 3.30 (CW) 6.70 | ||
7 | 3 10 0.83 (CW) 9.17 | ||
8 | 4 2 3.20 (RL) 14.80 | ||
9 | 5 0 8.25 (CW) 11.75 | ||
6 0 3.30 (CW) 16.70 | |||
7 0 0.83 (CW) 19.17 | |||
8 0 3.20 (RL) 16.80 | |||
9 0 0 20.00 | |||
--------------Add after 20hr annealing----------------- | --------------Add after 20hr annealing----------------- | ||
10 0 8.25 (CW) 13.75 (want to get to 22ul total volume because need to mimic the extra 2ul of AmpLigase Buffer) | |||
11 0 3.20 (RL) 18.80 | |||
--------------Add after 4hr gap-filling/circularization--------- | --------------Add after 4hr gap-filling/circularization--------- | ||
12 0 8.25 (CW) 15.75 (want to get to 24ul total volume because need to mimic the extra 2ul SLN mix) | |||
13 0 3.20 (RL) 20.80 | |||
===Probe+Template+Buffer Mix=== | ===Probe+Template+Buffer Mix=== | ||
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*We are using HemloKlenTaq for the reaction (because AmpliTaq Stoffel was discontinued) | *We are using HemloKlenTaq for the reaction (because AmpliTaq Stoffel was discontinued) | ||
*Mastermix recipe | *Mastermix recipe | ||
Component Stock conc Final conc 1x(ul) MM Vol ( | Component Stock conc Final conc 1x(ul) MM Vol (13x) (ul) | ||
Hemo KlenTaq 100% 20% 0.4 | Hemo KlenTaq 100% 20% 0.4 5.2 | ||
AmpLigase 5U/ul 0.5U/ul 0.2 | AmpLigase 5U/ul 0.5U/ul 0.2 2.6 | ||
dNTP 1000uM 100uM 0.2 | dNTP 1000uM 100uM 0.2 2.6 (MDA dNTP = 25mM, so do 1/25d) | ||
10x AmpLigase Buff 10x 1x 0.2 | 10x AmpLigase Buff 10x 1x 0.2 2.6 | ||
H2O 1.0 | H2O 1.0 13 | ||
*Thermocycler (continued): Add 2ul SLN to each rxn -> '''Incubate 60C 4hr''' -> 94C 2min -> add 2ul ExoI/ExoIII mix (1:1) -> 37C 2hr -> 94C 5min -> Hold | *Thermocycler (continued): Add 2ul SLN to each rxn (1->11) -> '''Incubate 60C 4hr''' -> 94C 2min -> add 2ul ExoI/ExoIII mix (1:1) to each rxn (1->13) -> 37C 2hr -> 94C 5min -> Hold 10C | ||
**Note: Right before 4hr is up, prep the ExoI/ExoIII mix at 1:1 ratio | **Note: Right before 4hr is up, prep the ExoI/ExoIII mix at 1:1 ratio | ||
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6 = 37C 2:00:00 | 6 = 37C 2:00:00 | ||
7 = 95C 5:00 | 7 = 95C 5:00 | ||
8 = | 8 = 10C Forever |
Revision as of 18:07, 18 August 2014
Target capture with padlock probes (designed 5/12) test with Rui's probes as control
Background
- So far, I have not gotten a good probe capture result yet (as the result of capture is usually a small band while mine is currently still a smear on the gel after PCR)
- One of the suggestions given in the previous lab meeting was the increase the number of controls during each run of the experiments. Because of this, I'll be adding a new negative control to be added in after 20hr annealing but before Hemo KlenTaq gap filling and circularization. I'll also be adding in a reaction for Rui's probe as a positive control
- Note that for Rui's probes, I'll need to do a 60C annealing. Also, Rui uses 3.2ul of 0.1ng/ul (need to dilute 1/10 from the 1ng/ul aliquot that she gave me) probe for 20ng of gDNA. So, for my experiment, will need to add 16ul of 0.1ng/ul probe for 100ng gDNA. This amounts to a 1000:1 probe:target ratio.
- Also will try a condition with lower probe:target ratio, as this may be a possibility for the high intensity of the non-specific band.
Procedure
Calculation of mass of probe required for each human gDNA input
- Can find calculation on my Google Doc at <https://docs.google.com/spreadsheets/d/10hhMyThBT2nAvxIodQq_1q0RQopnfMlNzSEZEexi0nE/edit?usp=sharing>
- For each of the tests, the following is the probe and target masses required:
rxn Target (ng) Probe:Target Probe (ng) 1 100ng 500:1 8.25 (my probe designed 5/12, on 100ng) 2 100ng 200:1 3.30 (my probe designed 5/12, on 100ng) 3 100ng 50:1 0.83 (my probe designed 5/12, on 100ng) 4 100ng 1000:1 0.32 (Rui's probe, on 20ng) 5 0ng(NTC, CW) 500:1 8.25 (This is NTC for 20hr probe annealing) 6 0ng(NTC, CW) 200:1 3.30 (This is NTC for 20hr probe annealing) 7 0ng(NTC, CW) 50:1 0.83 (This is NTC for 20hr probe annealing) 8 0ng(NTC, RL) 1000:1 0.32 (This is NTC for 20hr probe annealing) 9 0ng(NTC) ---- 0 (This is full NTC, no template and no probe) --------------------------------------------------------------------------------------------------------------------------------------------------- 10 0ng(NTC, CW) 500:1 8.25 (This is NTC for the 4hr gap-filling and circularization step, to be added AFTER annealing step) 11 0ng(NTC, RL) 1000:1 0.32 (This is NTC for the 4hr gap-filling and circularization step, to be added AFTER annealing step) --------------------------------------------------------------------------------------------------------------------------------------------------- 12 0ng(NTC, CW) 500:1 8.25 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization) 13 0ng(NTC, RL) 1000:1 0.32 (This is NTC for Exo digestion step, to be added AFTER gap-filling and circularization)
- Dilute my probe mix to 1ng probe/ul (will dilute probes produced on 7/10, which was ~14ul, ~60ng/ul)
- Probe concentration is ~60ng/ul -> 1/60d -> 1ul probe + 59ul water (save this for later so will not need to dilute so many times)
- Dilute Rui's probe mix to 0.1ng/ul
- Probe concentration is ~1ng/ul -> 1/10d -> 2ul probe + 18ul water
- Dilute target human gDNA concentration to 10ng/ul
- gDNA concentration is ~110ng/ul -> 1/11d -> 4ul gDNA + 40ul water
- Final volume of probe and target to add to each rxn
rxn Target (ul) Probe (ul) Water (ul) -> to get to 20ul total volume 1 10 8.25 (CW) 1.75 2 10 3.30 (CW) 6.70 3 10 0.83 (CW) 9.17 4 2 3.20 (RL) 14.80 5 0 8.25 (CW) 11.75 6 0 3.30 (CW) 16.70 7 0 0.83 (CW) 19.17 8 0 3.20 (RL) 16.80 9 0 0 20.00 --------------Add after 20hr annealing----------------- 10 0 8.25 (CW) 13.75 (want to get to 22ul total volume because need to mimic the extra 2ul of AmpLigase Buffer) 11 0 3.20 (RL) 18.80 --------------Add after 4hr gap-filling/circularization--------- 12 0 8.25 (CW) 15.75 (want to get to 24ul total volume because need to mimic the extra 2ul SLN mix) 13 0 3.20 (RL) 20.80
Probe+Template+Buffer Mix
- Add 2.00ul of 10x AmpLigase buffer to each reaction tube
- Overlay with 40ul mineral oil (can centrifuge in order for oil and solution to separate)
- Thermocycler: 95C 30sec -> cool down to 60C at 0.02C/sec -> Incubate 60C 20hr
Prep SLN mix solution
- We are using HemloKlenTaq for the reaction (because AmpliTaq Stoffel was discontinued)
- Mastermix recipe
Component Stock conc Final conc 1x(ul) MM Vol (13x) (ul) Hemo KlenTaq 100% 20% 0.4 5.2 AmpLigase 5U/ul 0.5U/ul 0.2 2.6 dNTP 1000uM 100uM 0.2 2.6 (MDA dNTP = 25mM, so do 1/25d) 10x AmpLigase Buff 10x 1x 0.2 2.6 H2O 1.0 13
- Thermocycler (continued): Add 2ul SLN to each rxn (1->11) -> Incubate 60C 4hr -> 94C 2min -> add 2ul ExoI/ExoIII mix (1:1) to each rxn (1->13) -> 37C 2hr -> 94C 5min -> Hold 10C
- Note: Right before 4hr is up, prep the ExoI/ExoIII mix at 1:1 ratio
Thermocycler Program (P-CAP on gradient PCR machine)
1 = 95C 0:30 2 = 94.8C 0:30 -0.2C per cycle 3 = Goto 2, 173 times 4 = 60C Forever (20hr -> add SLN -> 4hr) 5 = 94C 2:00 6 = 37C 2:00:00 7 = 95C 5:00 8 = 10C Forever