Difference between revisions of "Team:Newcastle/Measurement/Methods"

Line 69: Line 69:
 
         <div class="row about-desc" data-aos="fade-up">
 
         <div class="row about-desc" data-aos="fade-up">
 
             <div class="col-full">
 
             <div class="col-full">
 +
 +
<div class="row section-header has-bottom-sep" data-aos="fade-up">
 +
            <div class="col-full">
 +
                <h3 class="subhead">Plate Reader Set-up</h3>
 +
</div>
 +
<p>Culture absorbance and fluorescence were measured in 96 well plates using a Thermofisher Varioskan Lux plate reader (Thermofisher scientific) unless stated otherwise. Absorbance was measured at 600nm. GFP Fluorescence was measured at 525nm with excitation at 485nm. RFP fluorescence was measured at 635nm with excitation at 588nm. All readings took place at 25°C after a 5 second 300rpm shake step to homogenise the culture. Readings used a 12nm bandpass width and pathlength correction was disabled, as per the iGEM Interlab study guidelines. </p>
 +
</div>
 +
 +
        <div class="row services-list block-1-2 block-tab-full">
 +
 +
        <div class="row about-desc" data-aos="fade-up">
 +
            <div class="col-full">
 +
  
  

Revision as of 12:25, 17 October 2018

Alternative Roots

Alternative Roots

Materials and Methods

Scroll Down
Scroll Down

Materials and Methods used regarding Measurement, Automation and Reproducibility

Bacterial Strains.

Transformations with, and expression of, iGEM test devices and controls were carried out using chemically competent Escherichia coli DH5α. Competency was conferred using the MgCl-CaCl2 method (Sambrook and Russell 2001). Briefly, a single colony of DH5α was incubated in Leuria Bertoni (LB) broth overnight at 37°C with shaking at 220rpm. Overnight culture was diluted 1:100, further incubated until an optical density (OD600nm) of 0.3 – 0.6 was reached and then placed on ice for 30 minutes. Cells were centrifuged at 4000g for 5 minutes at 4°C, resuspended in 0.1M MgCl2 and incubated on ice for 30 minutes. The suspension was centrifuged again as before, resuspended in 0.1M CaCl2 and placed on ice for 30 minutes. Cells were spun down again, resuspended in 0.1M CaCl2 with 15% glycerol and frozen at -80°C.

Plate Reader Set-up

Culture absorbance and fluorescence were measured in 96 well plates using a Thermofisher Varioskan Lux plate reader (Thermofisher scientific) unless stated otherwise. Absorbance was measured at 600nm. GFP Fluorescence was measured at 525nm with excitation at 485nm. RFP fluorescence was measured at 635nm with excitation at 588nm. All readings took place at 25°C after a 5 second 300rpm shake step to homogenise the culture. Readings used a 12nm bandpass width and pathlength correction was disabled, as per the iGEM Interlab study guidelines.