Matt:LabNotes/2016-4-23: Difference between revisions
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>Mzcai (Created page with "=Test Diffusion of PA Gel Formulations= *Using PKP2 Beads as targets *PKP2_controlPP ==Dilute PKP2_controlPP== *Resuspended to 10uM with 450ul H2O...") |
>Mzcai m (→Protocol) |
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#Add mix to sample and incubate for 30min at 37C | #Add mix to sample and incubate for 30min at 37C | ||
#Move sample to 60C and oven slowly decreases to 55C and held for ~24hr | #Move sample to 60C and oven slowly decreases to 55C and held for ~24hr | ||
===Day 2=== | ===Day 2=== | ||
#Wash with 1X PBS once | #Wash with 1X PBS once | ||
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| Total||200 | | Total||200 | ||
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===Day 3=== | ===Day 3=== | ||
*Dish1 showed signs of leaking but the gel was not dried out and there was still some liquid on top | *Dish1 showed signs of leaking but the gel was not dried out and there was still some liquid on top |
Revision as of 19:17, 24 April 2016
Test Diffusion of PA Gel Formulations
- Using PKP2 Beads as targets
- PKP2_controlPP
Dilute PKP2_controlPP
- Resuspended to 10uM with 450ul H2O
- Serial dilute to 10nM
- 10:1 dilution 3 times
Experiment Plan
- Goal: Test whether padlock probes and polymerases can diffuse through ~100um? polyacrylamide hydrogel to generate rolonies
- Dish1: Positive control: mix beads into hydrogel solution before polymerization
- This way some beads will be close to the surface, minimizing distance molecules need to diffuse
- Can't do it without hydrogel matrix because the beads and rolonies need some sort of substrate
- Dish2: 5% Polyacrylamide Gel (199:1 Acrylamide:Bis-acrylamide)
- Beads are underneath gel, being held in place by magnets
- Do padlock probe capture and then RCA to generate rolonies in hydrogel matrix
Protocol
Day 1
- Gels are sitting in 1X PBS at 4C
- Prepare Ampligase mix on ice
- Preheat H2O + Padlock probes to 85C and then snap cool before adding Ampligase buffer and enzyme
Component | Volume |
DEPC-H2O | 70 |
Ampligase Buffer | 10 |
PKP2_controlPP 10nM | 10 |
Ampligase | 10 |
Total | 100 |
- Add mix to sample and incubate for 30min at 37C
- Move sample to 60C and oven slowly decreases to 55C and held for ~24hr
Day 2
- Wash with 1X PBS once
- Add 1uM FISSEQ_ppRCA (1ul 200uM FISSEQ_ppRCA + 199ul 2X SSC + 30% formamide) and incubate 1hr at 55C
- Preheated to 70C before adding
- Wash with 2X SSC once, 1X SSC once, and 1X PBS once
- Add RCA mix and incubate 15hr at 30C
Component | Volume |
H2O | 174 |
10X Phi29 Buffer | 20 |
25mM dNTP | 2 |
4mM aa-dUTP | 2 |
Phi 29 (low conc) | 2 |
Total | 200 |