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Team:Shenzhen BGIC ATCG/safety
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| + | <h1>Basic Safety Questions for iGEM 2013</h1><p class="s3">a. Please describe the chassis organism(s) you will be using for this project. If you will be using more than one chassis organism, provide information on each of them:</p><table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td/><td><p class="s4">Species</p></td><td><p class="s4">Strain no/name</p></td><td><p class="s4">Risk</p><p class="s4">Group</p></td><td><p class="s4">Risk group source link</p></td><td><p class="s4">Disease risk to humans? If so, which disease?</p></td></tr><tr><td><p class="s4">Ex</p></td><td><p class="s5">E. coli <span class="s4">(K 12)</span></p></td><td><p class="s4">NEB 10 Beta</p></td><td><p class="s4">1</p></td><td><p class="s4">www.absa.org/riskgroups/bacteria search.php?genus=&species=coli</p></td><td><p class="s4">Yes. May cause irritation to skin, eyes, and respiratory tract, may affect kidneys.</p></td></tr><tr><td><p class="s4">1</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">2</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">3</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">4</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">5</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">6</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">7</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">8</p></td><td/><td/><td/><td/><td/></tr></table><p>*For additional organisms, please include a spreadsheet in your submission.<br/>2. Highest Risk Group Listed:<br/>1 Greater than 1<br/>If you answered 1+, please also complete the iGEM Biosafety form part 2 for any organisms in this category.<br/>3. List and describe <i>all </i>new or modified coding regions you will be using in your project. (If you use parts from the 2013 iGEM Distribution without modifying them, you do not need to list those parts.)</p><table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td/><td><p class="s4">Part number.</p></td><td><p class="s4">Where did you get the physical DNA for this part (which lab, synthesis company, etc)</p></td><td><p class="s4">What species does this part originally come from?</p></td><td><p class="s4">What is the Risk Group of the species?</p></td><td><p class="s4">What is the function of this part, in its parent species?</p></td></tr><tr><td><p class="s4">Ex</p></td><td><p class="s4">BBa_C0040</p></td><td><p class="s4">Synthesized, Blue</p><p class="s4">Heron</p></td><td><p class="s4">Acinetobacter baumannii</p></td><td><p class="s4">2</p></td><td><p class="s4">Confers tetracycline resistance</p></td></tr></table><table border="1" cellspacing="0" style="border-collapse:collapse"><tr><td><p class="s4">1</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">2</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">3</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">4</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">5</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">6</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">7</p></td><td/><td/><td/><td/><td/></tr><tr><td><p class="s4">8</p></td><td/><td/><td/><td/><td/></tr></table><p>*For additional coding regions, please include a spreadsheet in your submission.<br/><br/>4. Do the biological materials used in your lab work pose any of the following risks? Please describe. a. Risks to the safety and health of team members or others working in the lab?<br/>b. Risks to the safety and health of the general public, if released by design or by accident?<br/><br/>c. Risks to the environment, if released by design or by accident?<br/><br/>d. Risks to security through malicious misuse by individuals, groups, or countries?<br/><br/>5. If your project moved from a small-scale lab study to become widely used as a commercial/industrial product, what new risks might arise? (Consider the different categories of risks that are listed in parts a-d of the previous question.) Also, what risks might arise if the knowledge you generate or the methods you develop became widely available? (Note: This is meant to be a somewhat open-ended discussion question.)<br/><br/>6. Does your project include any design features to address safety risks? (For example: kill switches, auxotrophic chassis, etc.) Note that including such features is not mandatory to participate in iGEM, but many groups choose to include them.<br/><br/>7. What safety training have you received (or plan to receive in the future)? Provide a brief description, and a link to your institution’s safety training requirements, if available.<br/><br/>8. Under what biosafety provisions will / do you work?<br/>a. Please provide a link to your institution biosafety guidelines.<br/><br/>b. Does your institution have an Institutional Biosafety Committee, or an equivalent group? If yes, have you discussed your project with them? Describe any concerns they raised with your project, and any changes you made to your project plan based on their review.<br/><br/>c. Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.<br/><br/>d. According to the <span class="s9">WHO Biosafety Manual</span>, what is the BioSafety Level rating of your lab? (Check the summary table on page 3, and the fuller description that starts on page 9.) If your lab does not fit neatly into category 1, 2, 3, or 4, please describe its safety features [see 2013.igem.org/Safety for help].<br/><br/>e. What is the Risk Group of your chassis organism(s), as you stated in question 1? If it does not match the BSL rating of your laboratory, please explain what additional safety measures you are taking.<br/><span></span><br/><br/><br/>Faculty Advisor Name: Faculty Advisor Signature:</p> | ||
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Revision as of 16:38, 26 September 2013
Playing with my eyes
aren't you?
Hi I am Dr. Mage!
A "budding" yeast cell!
Q & A
a. Please describe the chassis organism(s) you will be using for this project. If you will be using more than one chassis organism, provide information on each of them:
3 . List and describe all new or modified coding regions you will be using in your project. (If you use parts from the 2013 iGEM Distribution without modifying them, you do not need to list those parts.)
4 . Do the biological materials used in your lab work pose any of the following risks? Please describe.
5 . If your project moved from a small- scale lab study to become widely used as a commercial/industrial product, what new risks might arise? (Consider the different categories of risks that are listed in parts a - d of the previous question.) Also, what risks might arise if the knowledge you generate or the met hods you develop became widely available? (Note: This is meant to be a somewhat open - ended discussion question.)
6 . Does your project include any design features to address safety risks? (For example: kill switches, auxotrophic chassis, etc.) Note that including such features is not mandatory to participate in iGEM, but many groups choose to include them.
7 . What safety training have you received (or plan to receive in the future)? Provide a brief description, and a link to your institution’s safety training requirements, if available.
8.Under what biosafety provisions will / do you work?
Basic Safety Questions for iGEM 2013
a. Please describe the chassis organism(s) you will be using for this project. If you will be using more than one chassis organism, provide information on each of them:
Species | Strain no/name | Risk Group | Risk group source link | Disease risk to humans? If so, which disease? | |
Ex | E. coli (K 12) | NEB 10 Beta | 1 | www.absa.org/riskgroups/bacteria search.php?genus=&species=coli | Yes. May cause irritation to skin, eyes, and respiratory tract, may affect kidneys. |
1 | |||||
2 | |||||
3 | |||||
4 | |||||
5 | |||||
6 | |||||
7 | |||||
8 |
*For additional organisms, please include a spreadsheet in your submission.
2. Highest Risk Group Listed:
1 Greater than 1
If you answered 1+, please also complete the iGEM Biosafety form part 2 for any organisms in this category.
3. List and describe all new or modified coding regions you will be using in your project. (If you use parts from the 2013 iGEM Distribution without modifying them, you do not need to list those parts.)
Part number. | Where did you get the physical DNA for this part (which lab, synthesis company, etc) | What species does this part originally come from? | What is the Risk Group of the species? | What is the function of this part, in its parent species? | |
Ex | BBa_C0040 | Synthesized, Blue Heron | Acinetobacter baumannii | 2 | Confers tetracycline resistance |
1 | |||||
2 | |||||
3 | |||||
4 | |||||
5 | |||||
6 | |||||
7 | |||||
8 |
*For additional coding regions, please include a spreadsheet in your submission.
4. Do the biological materials used in your lab work pose any of the following risks? Please describe. a. Risks to the safety and health of team members or others working in the lab?
b. Risks to the safety and health of the general public, if released by design or by accident?
c. Risks to the environment, if released by design or by accident?
d. Risks to security through malicious misuse by individuals, groups, or countries?
5. If your project moved from a small-scale lab study to become widely used as a commercial/industrial product, what new risks might arise? (Consider the different categories of risks that are listed in parts a-d of the previous question.) Also, what risks might arise if the knowledge you generate or the methods you develop became widely available? (Note: This is meant to be a somewhat open-ended discussion question.)
6. Does your project include any design features to address safety risks? (For example: kill switches, auxotrophic chassis, etc.) Note that including such features is not mandatory to participate in iGEM, but many groups choose to include them.
7. What safety training have you received (or plan to receive in the future)? Provide a brief description, and a link to your institution’s safety training requirements, if available.
8. Under what biosafety provisions will / do you work?
a. Please provide a link to your institution biosafety guidelines.
b. Does your institution have an Institutional Biosafety Committee, or an equivalent group? If yes, have you discussed your project with them? Describe any concerns they raised with your project, and any changes you made to your project plan based on their review.
c. Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.
d. According to the WHO Biosafety Manual, what is the BioSafety Level rating of your lab? (Check the summary table on page 3, and the fuller description that starts on page 9.) If your lab does not fit neatly into category 1, 2, 3, or 4, please describe its safety features [see 2013.igem.org/Safety for help].
e. What is the Risk Group of your chassis organism(s), as you stated in question 1? If it does not match the BSL rating of your laboratory, please explain what additional safety measures you are taking.
Faculty Advisor Name: Faculty Advisor Signature:
