Team:BIT/interlab.html

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<h3>Summary</h3>
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<p>BBa_J23101+BBa_E0240</p>  
<p>BBa_J23101+BBa_E0240</p>  
<p>BBa_J23115+BBa_E0240</p>  
<p>BBa_J23115+BBa_E0240</p>  
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<p>Dh5a(全式金) Ecoli cell</p>
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<p>Dh5a Ecoli cell</p>
<p>Atibiotics(Sigma)</p>
<p>Atibiotics(Sigma)</p>
<p>LB culture medium</p>
<p>LB culture medium</p>

Revision as of 22:04, 17 October 2014

<!DOCTYPE html> radiation measurement

Summary

The Interlab study aims at collecting the data of three specific GFP (BBa_I20260, BBa_J23101+BBa_E0240 and BBa_J23115+BBa_E0240)expression devices measured by iGEM teams all over the world, thus to promote the business of standardized measurement. Our team are in the Measurement Track of iGEM this year, and we are involved in Interlab study according to the Measurement requirements.

Our interlab work was carried out With the DH5a as an expression host, and the Thermo Scientific Varioskan Flash spectral scanning as the equipment. We transfer the three devices into E.coli cells separately. And we measure the fluorescence data and optical density data with spectral scanning machine every 1 hour during a 8 hours cultivation. And we also apply the dilution operation to the sample considering the OD interference.

Methods

We use endonuclease (EcoRI and PstI, XbaI and PstI) and T4 DNA ligase(NEB) to construct them. Finally, the ligation product was introduced into the pSB1C3. All constructs used were transformed into DH5α cells.

The cultivation of our bacteria was performed in tubes filled with 5 mL LB medium. The cultures were kept at 37 °C and 150 rpm in shaker. Antibiotics were added to each media (kanamycin 58 µg/mL for I20260, chloramphenicol 170 µg/mL for B0015, J23101.E0240 and J23115.E0240).

We incubate the bacteria in a constant temperature for 12 hours , then we put 50μL cultivated mass in tubes per hour, each group keeps three parallel samples. After obtaining eight or more gradients, we transfer the culture liquid 150μL per tube into a 96-wells plate to do the measurement.

Measurement of fluorescence and OD were performed using the Thermo Scientific Varioskan Flash with the 'Thermo Scientific SkanIt' software and with the 96-Well Multiwell Plates(Corning).

And the measurement software we used is listed below: cited from http://www.thermo.com.cn/Resources/200802/productPDF_30632.pdf

Material&equipment

BBa_I20260

BBa_J23101+BBa_E0240

BBa_J23115+BBa_E0240

Dh5a Ecoli cell

Atibiotics(Sigma)

LB culture medium

Corning 96-Well Multiwell Plates

Thermo Scientific Varioskan Flash

* We use these parts of BioBricks, I20260, J23101+E0240 and J23115+E0240. The I20260 is settled in a pSB3K3 with an insert set, which consists of the combination of the promoter J23101, the RBS B0032, the GFP coding sequence E0040 and the terminator B0015. The second part has the same insert as I20260, but uses pSB1C3 as a carrier. There is only one difference between the latter two that J23115+E0240 using another promoter called J23115.

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