Matt:LabNotes/2014-2-21: Difference between revisions
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*In wells: F7 and F8 | *In wells: F7 and F8 | ||
*Check with 1uM dcProbe2RevComp-Cy3 (ATTO488) dye-probe | *Check with 1uM dcProbe2RevComp-Cy3 (ATTO488) dye-probe | ||
====Result==== | |||
*No signal -> Dye doesn't have non-specific binding to primary rolonies | |||
===Checking MALAT1, RAB7A, and ACTB Targets in RandomHex Primary Rolonies=== | ===Checking MALAT1, RAB7A, and ACTB Targets in RandomHex Primary Rolonies=== |
Latest revision as of 04:41, 28 February 2014
Screening 32 wells for Ampligase Positive Control Test[edit]
- Using 32 wells of 96-well plate Matt:LabNotes/2014-1-24
- Used microscope to check cell density and morphology in each well to pick the best wells for this experiment
- Color coded each well based on quality of cells
- Designated 2 or 4 wells for each sample group
- All wells will have 0.5 U Ampligase/ul except for 2 Fixed Template wells
Mark & Find Pos -> Well[edit]
- E6 : Pos 1
- F6 : Pos 2
- F7 : Pos 3
- F8 : Pos 4
- F9 : Pos 5
- F10 : Pos 6
- C7 : Pos 7
- C8 : Pos 8
- C9 : Pos 9
- C10 : Pos 10
- D7 : Pos 11
- E7 : Pos 12
Checking MALAT1 Targets in 1000nt RT_RAB7A[edit]
- In wells: F9 and F10
- Check with 1uM MALAT1_1stRolonyFISH (Cy3) dye-probe
Checking for non-specific binding of dcProbe2RevComp-Cy3[edit]
- In wells: F7 and F8
- Check with 1uM dcProbe2RevComp-Cy3 (ATTO488) dye-probe
Result[edit]
- No signal -> Dye doesn't have non-specific binding to primary rolonies
Checking MALAT1, RAB7A, and ACTB Targets in RandomHex Primary Rolonies[edit]
- In wells: E6 and F6
- Check with 1uM:
- MALAT1_1stRolonyFISH (Cy3) dye-probe
- RAB7A_1stRolonyFISH (ATTO550) dye-probe
- ACTB_1stRolonyFISH (ATTO488) dye-probe