Screening Colonies from 3/15 Electroporation for DiNV Presence Plate 10
- Made 2 new LB plates with chloramphenicol
- Made a solution of 45ul 100% ethanol and 45ul of stock chlor
- Spread 20ul of the chlor solution on 2 new LB plates
- Let the plates dry a little in the bacteria hood
- These plates had grids on them with numbers to keep track of the colonies (see below)
- Prepared a 96 well plate with strip caps with 5ul of molecular grade water in each well
- For each colony in plate 1 from the fridge:
- I picked it up with an autoclaved p2 tip
- I dabbed it lightly on the appropriate square in the gridded plate
- I swirled it for a few seconds in the appropriate well in the 96 well plate
- This took about and hour to 2 hours
- There were not very many colonies on this plate so I re-picked some colonies from plate 1A and 1B - starting on column 7 of the 96 well plate
The gridded plates were numbered like this:
Plate 10A:
1 | 2 | 3 | 4 | 5 |
---|---|---|---|---|
6 | 7 | 8 | 9 | 10 |
11 | 12 | 13 | 14 | 15 |
16 | 17 | 18 | 19 | 20 |
21 | 22 | 23 | 24 | 25 |
Plate 10B:
26 | 27 | 28 | 29 | 30 |
---|---|---|---|---|
31 | 32 | 33 | 34 | 35 |
36 | 37 | 38 | 39 | 40 |
41 | 42 | 43 | 44 | 45 |
46 | 47 | 48 | 49 | 50 |
And the 96 well plate:
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
A | 1 | 9 | 17 | 25 | 33 | 41 | 1 | 9 | 17 | 25 | 33 | 41 |
B | 2 | 10 | 18 | 26 | 34 | 42 | 2 | 10 | 18 | 26 | 34 | 42 |
C | 3 | 11 | 19 | 27 | 35 | 43 | 3 | 11 | 19 | 27 | 35 | 43 |
D | 4 | 12 | 20 | 28 | 36 | 44 | 4 | 12 | 20 | 28 | 36 | 44 |
E | 5 | 13 | 21 | 29 | 37 | 45 | 5 | 13 | 21 | 29 | 37 | 45 |
F | 6 | 14 | 22 | 30 | 38 | 46 | 6 | 14 | 22 | 30 | 38 | 46 |
G | 7 | 15 | 23 | 31 | 39 | 47 | 7 | 15 | 23 | 31 | 39 | X |
H | 8 | 16 | 24 | 32 | 40 | 48 | 8 | 16 | 24 | 32 | 40 | X |
PCRs
- Then, the solution in the 96 well plate was used for colony PCR
- The general PCR protocol was used, however 1ul of the bacteria-water solution was used instead of DNA
- I used lef 4 as the primer to amplify DiNV DNA because it had not shown any off-target amplification before
- 16S is a control for bacteria presence in the sample
- PCR mixes:
reagent | lef 4 | 16S |
---|---|---|
GoTaq | 500ul | 500ul |
F primer | 25ul | 25ul |
R primer | 25ul | 25ul |
molec grade water | 350ul | 350ul |
Reactions were run for 30 cycles. Primer information can be found here.
The gels from this plate can be found here. No colony was positive for DiNV.