Difference between revisions of "Team:BostonU/Safety"
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<p style = "font-size:150%; padding:5px 150px 10px 150px; color:#0071A7;">All cloning in Top10 Chemically Competent E. coli on the benches of the BSL 1 area of the laboratory. All scientists wore pants, closed toed shoes, lab coats, and gloves. Our samples were either stored in parafilmed plates, in -80 centigrade stasis, or were bleached. All chemicals used during the cloning process (i.e. miniprep waste and ethidium bromide gels) were disposed of in appropriately labeled waste containers located around the lab.</p> | <p style = "font-size:150%; padding:5px 150px 10px 150px; color:#0071A7;">All cloning in Top10 Chemically Competent E. coli on the benches of the BSL 1 area of the laboratory. All scientists wore pants, closed toed shoes, lab coats, and gloves. Our samples were either stored in parafilmed plates, in -80 centigrade stasis, or were bleached. All chemicals used during the cloning process (i.e. miniprep waste and ethidium bromide gels) were disposed of in appropriately labeled waste containers located around the lab.</p> | ||
| − | <p style = "font-size:150%; padding:5px 150px 10px 150px; color:#0071A7;">Work with BSL2 materials centered around HEK293FT cells. While HEK cells are generally a BSL 1 cell line, the addition of a SV40 virus into our cells increased the biological safety concern. SV40 poses a cancer risk to scientists who choose to work with it. The same attire required for BSL 1 was worn in the BSL 2 Tissue | + | <p style = "font-size:150%; padding:5px 150px 10px 150px; color:#0071A7;">Work with BSL2 materials centered around HEK293FT cells. While HEK cells are generally a BSL 1 cell line, the addition of a SV40 virus into our cells increased the biological safety concern. SV40 poses a cancer risk to scientists who choose to work with it. The same attire required for BSL 1 was worn in the BSL 2 Tissue Culture room, with new gloves being changed every time students stepped out of each lab space. Students were also required to wear state certified eye protection. In addition to bleaching all samples upon the completion of experiments, all work was conducted within biological hoods with media traps. Every surface within those hoods was sterilized both preceding and at the conclusion of work with 70% ethanol.</p><br><br><br><br><br><br> |
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Revision as of 02:22, 16 October 2016
The greatest safety concerns that arose during our project surrounded the chassis used for both cloning and assaying our systems. Specifically, our chasses encompassed two distinct biological safety levels: BSL 1 and BSL2. Each level required different safety protocols as well training, which students received from both the RIMS program at Boston University and their Mentors.
All cloning in Top10 Chemically Competent E. coli on the benches of the BSL 1 area of the laboratory. All scientists wore pants, closed toed shoes, lab coats, and gloves. Our samples were either stored in parafilmed plates, in -80 centigrade stasis, or were bleached. All chemicals used during the cloning process (i.e. miniprep waste and ethidium bromide gels) were disposed of in appropriately labeled waste containers located around the lab.
Work with BSL2 materials centered around HEK293FT cells. While HEK cells are generally a BSL 1 cell line, the addition of a SV40 virus into our cells increased the biological safety concern. SV40 poses a cancer risk to scientists who choose to work with it. The same attire required for BSL 1 was worn in the BSL 2 Tissue Culture room, with new gloves being changed every time students stepped out of each lab space. Students were also required to wear state certified eye protection. In addition to bleaching all samples upon the completion of experiments, all work was conducted within biological hoods with media traps. Every surface within those hoods was sterilized both preceding and at the conclusion of work with 70% ethanol.
