Difference between revisions of "Team:UCLA/InterLab"
(Created page with "{{UCLA}} {{UCLA:Suffix}}") |
|||
| Line 2: | Line 2: | ||
{{UCLA:Suffix}} | {{UCLA:Suffix}} | ||
| + | |||
| + | <html> | ||
| + | |||
| + | <H1> 2016 Interlab Study </H1> | ||
| + | <h2><strong>Introduction</strong></h2> | ||
| + | The 2016 UCLA iGEM Team is proud to participate in the Third International InterLab Measurement Study in synthetic biology. As members of the synthetic biology community, we are committed to providing robust data for the development of novel characterization methods in the rapidly growing biological design fields of synthetic biology. The purpose of the 2016 InterLab study is to examine the precision and accuracy of fluorescence data and information processing from active iGEM teams participating around the world. By collecting fluorescence data from multiple teams in absolute units, variability in measurement and consistency of data collected from instrumentation following a uniform procedure can be determined within a high degree of accuracy. This notebook will record all protocols, daily experiments, relevant images, as well as the raw data and graphs used in the Interlab Submission Form. | ||
| + | |||
| + | <h3><strong>Protocols</strong></h3> | ||
| + | The main protocol applied for the 2016 Interlab Study was provided by iGEM Headquarters. The specific transformation protocol used was for New England Biolabs C2989K (E. coli K strain) and can be found <a href="://www.neb.com/protocols/1/01/01/electroporation-protocol-c2989"> here | ||
Revision as of 19:51, 7 October 2016
