Matt:LabNotes/2015-7-6: Difference between revisions
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>Mzcai (Created page with "=Test Mouse Embryo Pre-Processing Protocol for DARTFISH= * First Try failed due to white particles after RT **Used Embryoe #3 and #4 **Try one mor...") |
>Mzcai m (→Procedure) |
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===Procedure=== | ===Procedure=== | ||
#Make PBT: 1X PBS + 0.1% Triton X-100 | #Make PBT: 1X PBS + 0.1% Triton X-100 | ||
#Rehydrate embryo #7 in | #Rehydrate embryo #7 in 2ml original tube | ||
#*75% MeOH in PBT for 10min rotating | #*75% MeOH in PBT for 10min rotating | ||
#*50% MeOH in PBT for 10min rotating | #*50% MeOH in PBT for 10min rotating | ||
#**Embryo may have split in two? Maybe TX-100 concentration was too high in the 50% MeOH solution and needs to be remade | #**Embryo may have split in two? Maybe TX-100 concentration was too high in the 50% MeOH solution and needs to be remade | ||
#*25% MeOH in PBT for 10min rotating | #*25% MeOH in PBT for 10min rotating | ||
#*PBT for 10min rotating twice and add PBT to a second empty tube | #*PBT for 10min rotating twice and add PBT to a second empty 2ml centrifuge tube | ||
#Wash with 1X PBS three times for both tubes | #Wash with 1X PBS three times for both tubes | ||
#Make RT Mix (2X volume) '''on ice''' | #Make RT Mix (2X volume) '''on ice''' |
Revision as of 23:28, 6 July 2015
Test Mouse Embryo Pre-Processing Protocol for DARTFISH
- First Try failed due to white particles after RT
- Used Embryoe #3 and #4
- Try one more time with a control (no embryo) to see if white particles are degraded embryo or precipitate
ISH Protocol
- Protocol.pdf
- Fixed, dehydrated in methanol, and stored in -20C
- Rehydrated and permeabilized with ProK for ISH
Fixed samples
- File:MERT 2015-05-14 E7.5 FISSEQ.JPG
- Got 7 embryos each in a 2ml tube and stored in -20C
FISSEQ
- To save padlock probes will test fixation/permeabilization sample conditions with FISSEQ
- Will use universal probe for all rolonies (FISSEQ_Adpt Cy3?) to check
- To image, sandwich embryo between glass slide and coverslip
Procedure
- Make PBT: 1X PBS + 0.1% Triton X-100
- Rehydrate embryo #7 in 2ml original tube
- 75% MeOH in PBT for 10min rotating
- 50% MeOH in PBT for 10min rotating
- Embryo may have split in two? Maybe TX-100 concentration was too high in the 50% MeOH solution and needs to be remade
- 25% MeOH in PBT for 10min rotating
- PBT for 10min rotating twice and add PBT to a second empty 2ml centrifuge tube
- Wash with 1X PBS three times for both tubes
- Make RT Mix (2X volume) on ice
- H2O - 314ul
- M-MuLV RT Buffer 10X - 40ul
- dNTP 25mM- 4ul
- aa-dUTP 2mM- 8ul
- FISSEQ_RT primer (nonamer) 100uM - 10ul
- RNase Inhibitor 40U/ul- 4ul
- M-MuLV RTase 100U/ul- 20ul
- Add 200ul RT Mix to embryo tube and empty tube and incubate for 10min at 4C and then incubate overnight at 37C