The goal of the interlab study is to explore a major question: How close can the numbers be when fluorescence is measured all around the world? So we measure GFP fluorescence in our lab with plate reader (Tecan Infinite M200pro). This year, three devices and one positive control and one negative control were provided by the Registry. The results show increased fluorescence in the stronger promoter expected.

After the experiment, five required devices were created:
Positive control: I20270 in pSB1C3;
Negative control: R0040 in pSB1C3;
Test Device 1: J23101.BCD2.E0040.B0015 in pSB1C3;
Test Device 2: J23106.BCD2.E0040.B0015 in pSB1C3;
Test Device 3: J23117.BCD2.E0040.B0015 in pSB1C3;
Test Device 4: J23101+I13504 in pSB1C3;
Test Device 5: J23106+I13504 in pSB1C3;
Test Device 6: J23117+I13504 in pSB1C3.

I. Materials

• Competent cells ( Escherichia coli strain DH5α)
• LB (Luria Bertani) media
• Chloramphenicol (stock concentration 25 mg/mL dissolved in EtOH - working stock 25 ug/mL)
• 50 ml Falcon tube (or equivalent, preferably amber or covered in foil to block light)
• Incubator at 37°C
• 1.5 ml eppendorf tubes for sample storage
• Ice bucket with ice
• Pipettes

II. Cell measurement protocol

1. Transform 8 plasmids into DH5α competent cells, grown in incubator for 12 hrs at 37℃.
2. Pick 2 colonies from each of plate and inoculate it on 10mL LB medium and Chloramphenicol. Grow the cells for 16hrs at 37°C and 220rpm.
3. Cell growth, sampling, and assay.
4. Obtain initial OD 600 measurement of overnight cultures. Then dilute each sample to an OD of 0.02.
5. Incubate the cultures at 37°C and 220rpm. Take 100µL (1% of total volume) samples of the cultures at 0, 2, 4 and 6 hours of incubation.
6. At the end of sampling point measure these samples (OD and Fl measurement).
7. Measurements of absorbance and fluorescence:
(1) OD 600
Device: Plate Reader（Tecan Infinite M200pro） Wavelengths: 600 nm absorption.
(2) Fluorescence
Device: Plate Reader（Tecan Infinite M200pro）, 96-well plates. Wavelengths: 485 nm excitation, 530 nm emission.

I. OD 600 Reference point

Table 1. Absorbance at 600nm for LUDOX and H2O

II. Fluorescein standard curve

Table 2. Fluorescence measurements for fluorescein stock solution at decreasing concentration



Table 3. The Fluorescein Standard Curve in plate reader with 485nm excitation, 530nm emission



Fluorescein Standard Curve (log scale)

III. Cell Measurements

Click to view detailed charts.
1. OD600–Background
2. Fluorescence Background (485nm excitation, 530nm emission)
3. FI/ABS600
4. Summary Statistics
(1) Arithmetic Mean of FI/ABS600
(2) Arithmetic Standard Deviation of FI/ABS600
(3) Geometric Mean of FI/ABS600
(4) Geometric Standard Deviation of FI/ABS600

Q: Who did the actual work to acquire these measurements?
A: Yulong Han and Yang Liang.

Q: What other people should be credited for these measurements?
A: Yousi Fu.

Q: On what dates were the protocols run and the measurements taken?
A: Required devices were transformed on 14th August, 2017. All samples were measured on 15th August, 2017.

[1] Anderson, C., Berkley iGEM Team., Anderson Promoter Collection. Registry of Standard Biological Parts, 2006
[2] http://parts.igem.org/Promoters/Catalog/Anderson[Accessed 2014.09.19]
[3] https://2016.igem.org/Team:XMU-China/Interlab
[4] https://2015.igem.org/Team:Amoy/Interlab