Difference between revisions of "Team:UNITN-Trento/Test"

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<h2><strong> Safety </strong></h2>
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<h2><strong>Notebook</strong></h2>
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<p> Work hard, work safe </p>
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<p>Check out our experiments by selecting one of the sections we have worked in!</p>
 
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<p>We have reviewed our organisms and parts against the <a class="i_linker" href="https://2015.igem.org/Safety/WhiteList" target="_blank">White List</a>. All the parts and bacterial strains that we used are in the <span class="i_enph">Risk Group 1</span></p>
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<p>We have submitted to iGEM headquarters <span class="i_enph">“About Our Lab”</span> and <span class="i_enph">“About Our Project”</span> questionnaires by the June 26<sup>th</sup> deadline</p>
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<p>We have submitted to iGEM headquarters the <span class="i_enph">“Final Safety Form”</span> by the August 28<sup>th</sup> deadline</p>
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<p>We, the UNITN iGEM Team want to follow high standards of safe and responsible biological engineering. Before entering the lab we attended mandatory on-line courses regarding lab safety with final tests. In particular we focused on the following topics:</p>
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<p>We also attended the “Health and safety at the workplace” course, which is mandatory for all students and workers at the University of Trento.</p>
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<p class="question">What happens when it's all used up? Will it be sterilized, discarded, or recycled?</p>
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<p>All the parts we used throughout the project are NOT toxic or dangerous for  humans or the environment. We neither worked with proteins toxic themselves, nor we used enzymes that synthesize toxic molecules. In addition to basic parts from the registry (i.e. RBS, promoters, β-carotene, etc), we also used two genes from the SAR86 uncultured bacteria. These genes are proteorhodopsin, which was extracted from the Registry (BBa_K773002) and blh (15,15’-β-carotene dioxygenase), which was synthesized by Genescript. There is no associated risk level with the uncultured bacteria SAR86, however we are using only DNA sequences that encodes for genes, which carry distinct functions that are no harmful to humans, or the environment. We have clarified this issue with iGEM Safety Office.</p>
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<p>We did <span class="i_enph">NOT</span> use any virulence factors in our organisms.</p>
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<p>All the bacterial strains used are from Risk Group 1. We used the following strains:</p>
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<li> K12 - NEB 10-beta E. coli</li>
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<li> K12 - JM109 E. coli</li>
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<li> BL21 - NEB Express E. coli</li>
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<p>Last but non least we adopted the appropriate PPE during the lab work.  We always used lab coats, nitrile gloves and goggles.  We safely operated with biological material under the laminar flow cabinet BioAir SAFEMATE Series Class II 1.8.</p>
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<p>We used chemicals that are associated with hazard (ethidium bromide, azide,  organic solvents) under the chemical hood Fume Hood MOD. ASEM® 120EN New - Class 0.</p>
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<p>We carefully revised all the Material Safety Datasheet of each compound that was  used prior to start an experiment.</p> 
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Revision as of 14:07, 21 August 2015

Notebook

Check out our experiments by selecting one of the sections we have worked in!

  • Introduction

  • Experimental
    Design

  • Protocols

  • Final Discussion