Difference between revisions of "Team:Manchester/Safety"

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Safety is absolutely paramount in the scientific research area.  In conducting scientific experiments, researchers should always comply to the safety measurements outlined in the Health and Safety at Work Act 1974, c.37 [1], not only to protect themselves, but also the members of the public and environment from any potential harm.
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Safety is absolutely paramount in the scientific research area.  In conducting scientific experiments, researchers should always comply to the safety measurements outlined in the Health and Safety at Work Act 1974, c.37 <sup>[1]</sup>, not only to protect themselves, but also the members of the public and environment from any potential harm.
 
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Scroll to check out the safety measurements we took!   
 
Scroll to check out the safety measurements we took!   
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   <li>Hazard statements: H302, H330, H341</li>
 
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   <li>Risks: Harmful if swallowed and inhaled, highly mutagenic and may be carcinogenic [3].</li>
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   <li>Risks: Harmful if swallowed and inhaled, highly mutagenic and may be carcinogenic <sup>[3]</sup>.</li>
 
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<p>Similar to EtBr, SYBR Safe enables the visualization of nucleic acid bands using agarose gels.  In comparison, SYBR Safe has been identified to be 4 to 5 times less mutagenic than EtBr [4].  Thus, we substituted EtBr with SYBR Safe for most of our nucleic acid staining procedures.
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<p>Similar to EtBr, SYBR Safe enables the visualization of nucleic acid bands using agarose gels.  In comparison, SYBR Safe has been identified to be 4 to 5 times less mutagenic than EtBr <sup>[4]</sup>.  Thus, we substituted EtBr with SYBR Safe for most of our nucleic acid staining procedures.
 
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<p>GOx catalyzes the oxidation of glucose to hydrogen peroxide (H2O2) and D-glucono-δ-lactone. GOx is used in our pilot experiment [link to pilot experiment data] to justify our proof of concept before we kick start our actual project [link to mechanism 1 page] with alcohol oxidase (AOx).
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<p>GOx catalyzes the oxidation of glucose to hydrogen peroxide (H2O2) and D-glucono-δ-lactone. GOx is used in our <a src="">pilot experiment </a> to justify our proof of concept before we kick start our <a src="">actual project </a> with alcohol oxidase (AOx).
 
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HRP catalyzes the redox reaction and amplify the signals of chromogenic (eg: ABTS) and chemiluminescence (eg: luminol) substrates.  The reaction is fast and visible, as shown in our pilot study [link to pilot study].
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HRP catalyzes the redox reaction and amplify the signals of chromogenic (eg: ABTS) and chemiluminescence (eg: luminol) substrates.  The reaction is fast and visible, as shown in our <a src="">pilot study </a>.
 
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Revision as of 18:22, 19 September 2016

Manchester iGEM 2016
safety summary

Safety is absolutely paramount in the scientific research area. In conducting scientific experiments, researchers should always comply to the safety measurements outlined in the Health and Safety at Work Act 1974, c.37 [1], not only to protect themselves, but also the members of the public and environment from any potential harm.

Scroll to check out the safety measurements we took!

safe project design
choose a non-pathogenic chassis
safety table
choose a non-pathogenic chassis

Ethidium Bromide (EtBr)

  • Hazard statements: H302, H330, H341

  • Risks: Harmful if swallowed and inhaled, highly mutagenic and may be carcinogenic [3].

EtBr is commonly used in laboratories to identify the band sizes of DNA samples under ultraviolet light after being loaded onto agarose gels.

Usage of EtBr has been reduced in our lab by using SYBR Safe as a substitute to minimize the risks as stated above.

SYBR Safe

  • Hazard statements: H227

  • Risks: Flammable, may cause mild eye and skin irritation

Similar to EtBr, SYBR Safe enables the visualization of nucleic acid bands using agarose gels. In comparison, SYBR Safe has been identified to be 4 to 5 times less mutagenic than EtBr [4]. Thus, we substituted EtBr with SYBR Safe for most of our nucleic acid staining procedures.

ABTS

(2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid))

  • Hazards statements: H315, H319, H335

  • Risks: May cause skin, eye and respiratory irritation.

ABTS is widely used to detect the binding activity of molecules in presence of a peroxidase enzyme (eg: HRP).

The possibility of causing skin irritation when in direct contact with ABTS indicates that ABTS may not be the best candidate for our actual AlcoPatch. For future experiments, ABTS should be substituted with other safer redox indicators.

Glucose Oxidase (GOx)

  • Hazards statements: H334

  • Risks: May cause skin and respiratory irritation.
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GOx catalyzes the oxidation of glucose to hydrogen peroxide (H2O2) and D-glucono-δ-lactone. GOx is used in our pilot experiment to justify our proof of concept before we kick start our actual project with alcohol oxidase (AOx).

Horseradish Peroxidase (HRP)

  • Hazards statements: H334, H317

  • Risks: May cause skin and respiratory irritation.


HRP catalyzes the redox reaction and amplify the signals of chromogenic (eg: ABTS) and chemiluminescence (eg: luminol) substrates. The reaction is fast and visible, as shown in our pilot study .

Future Plans

  • Design a kill switch system to minimize that the risk of releasing live E.coli organisms to the environment.

  • Explore other redox indicators as alternatives for ABTS.