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#314 Molecular Biology Running

Transformation, pUC19-GFP into DH5α

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transformation cloning DH5α pUC19 amp-selection
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This template captures heat-shock transformation of chemically competent E. coli DH5α with the pUC19-GFP cloning vector.

Goal: introduce the pUC19-GFP plasmid into DH5α for plasmid amplification and downstream sequencing verification, with ampicillin selection on LB agar.

Method overview: Competent DH5α cells are thawed on ice, 50 ng of plasmid DNA is added, cells are incubated on ice for 30 minutes, heat-shocked at 42°C for 45 seconds, returned to ice for 2 minutes, recovered in 950 µL of SOC at 37°C with shaking for 1 hour, then plated on LB + ampicillin (100 µg/mL) and incubated overnight at 37°C. Colonies are counted the next morning and selected colonies are picked for sequencing verification and glycerol stock preparation.

Expected: 50-500 colonies on the experimental plate (efficiency ~10⁶ CFU/µg with DH5α and high-copy vector), zero colonies on the no-DNA control plate.

Last saved: 34 seconds ago
11 fields loaded from Bacterial Transformation baseline (Cloning SOP v1.3)
Sample
Competent strain
select
DH5α, TOP10, BL21(DE3), Stbl3, JM109
Plasmid
text
pUC19-GFP
DNA input amount
number
50ng
Transformation
Ice incubation
number
30min
Heat shock temp
number
42°C
Heat shock duration
number
45s
Post-shock on ice
number
2min
Recovery & Plating
Recovery medium
select
SOC, LB
Recovery time
number
60min
Plating volume
number
100µL
Selection antibiotic
text
Amp 100 µg/mL
pUC19-GFP_map.pdf
212 KB
plate_count_photo.png
1.8 MB
colony_pick_log.csv
14 KB
01
Pre-warm SOC + LB+Amp plates at 37°C
0:15
02
Thaw competent DH5α aliquot on ice (~10 min)
0:10
03
Add 50 ng pUC19-GFP to 50 µL cells, flick to mix
No-DNA ctrl tube in parallel
0:02
04
Incubate on ice 30 minutes
0:30
05
Heat shock 42°C × 45 s in water bath, return to ice 2 min
Recorded at 10:14 by AM
0:03
06
Add 950 µL SOC, recover at 37°C with shaking
225 rpm
1:00
07
Plate 100 µL on LB+Amp 100 (and 100 µL on no-DNA ctrl)
Spread with beads
0:10
08
Invert plates, incubate 37°C overnight (16-18 h)
17:00
09
Count colonies, calculate transformation efficiency
237 cfu / plate
0:20
10
Pick 8 colonies into LB+Amp for o/n culture + sequencing
Awaiting Mon AM
0:15
A B C D E F G
1 Plate Condition DNA (ng) Plated (µL) Colonies CFU/µg Notes
2 1 +DNA (pUC19-GFP) 50 100 237 4.74×10⁶ Good lawn-free spread
3 2 +DNA, 1:10 dilute 50 10 26 5.20×10⁶ Confirms plate 1 count
4 3 no-DNA ctrl 0 100 0 0 Clean, contamination ruled out
5 4 no-Amp ctrl 50 100 lawn na Cells viable
DH5α chemically competent E. coli
18265017 · Lot 2521403
In stock
pUC19-GFP plasmid prep (60 ng/µL)
PLM-0048 · Prep 2026-04
In stock
Ampicillin sodium salt (100 mg/mL)
A9518 · Lot SLBP1247V
In stock
SOC medium
15544034 · Lot 2401821
In stock
LB agar + 100 µg/mL Amp plates
Lab-poured · Batch 04-08
Low
X-gal / IPTG (for blue/white screen)
R0941 · Lot 26
In stock
DH5α competent aliquots (50 µL)
-80 °C · Freezer A-3 · Drawer 2 · Box CC-DH5α-04
×42
pUC19-GFP plasmid stock (60 ng/µL)
-20 °C · Freezer B-1 · Rack 4 · Tube P-048
×1
Glycerol stocks (transformed clones)
-80 °C · Freezer A-3 · Drawer 4 · Box GS-2026-04
×8 pending
Visibility
Marin LabA. Marin
Can write
A. MarinDr. J. Park




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