Team:GPHS Snohomish WA
From 2012hs.igem.org
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Protocol: | Protocol: | ||
- | 1 Make sure set-up is complete | + | 1 Make sure set-up is complete. |
- | 2 Add | + | 2 Add 200 microliters Cacl2 Solution to each tube. |
- | 3 | + | 3 Harvest NEBlO cells: |
Scrape off the plate for eact tube | Scrape off the plate for eact tube | ||
Resuspend all the tubes | Resuspend all the tubes | ||
- | 4 Add DNA to each tube | + | 4 Add DNA to each tube: |
- | + | 5 microliters of "RFP Control" to control tube | |
- | 2- | + | 2-5 microliters of other plasmids to labeled tubes |
- | 5 Incubate on ice for 5 | + | 5 Incubate on ice for 5 minutes. |
- | 6 Place in water bath for 90 seconds | + | 6 Place in hot water bath for 90 seconds. |
- | 7 Place tubes on ice for another minute | + | 7 Place tubes on ice for another minute. |
- | 8 Add | + | 8 Add 200 microliters of SOC media (pre-heated). |
- | 9 Label 3 plates, with appropiate drug | + | 9 Label 3 plates, with appropiate drug. |
- | 10 Add | + | 10 Add 200 microliters of transformed cells to plate, spread evenly. |
- | 11Put plates in incubator | + | 11Put plates in incubator. |
- | Our results were not what we were hoping because the growth of the cells did not occur. The cells | + | Our results were not what we were hoping because the growth of the cells did not occur. The cells were competent, but either they did not take in the plasmids or they did not survive the transfers between heat and cold. |
+ | 6/8/12 | ||
+ | We | ||
- | + | This first trial did not have our desired results. | |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | This first trial did not have our desired results | + | |
===Results/Conclusions=== | ===Results/Conclusions=== |
Revision as of 19:42, 15 June 2012
You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing. | |
Tell us more about your project. Give us background. Use this as the abstract of your project. Be descriptive but concise (1-2 paragraphs) | |
Team GPHS_Snohomish_WA |
Official Team Profile |
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Contents |
Arsenic Avengers
- Our team is located at Glacier Peak High School in Snohomish, WA.
- We have eight members.
- Our mentors are Eric Lagally, Ms. Caraballo,and Nick Chavkin (UW bioengineering).
Project Introduction
This semester was focused on introducing ourselves to the competition of iGEM, as well as determining our project. [http://en.wikipedia.org/wiki/Glacier_Peak_High_School The Grizzles] have come to the conclusion to utilize the genes in E. coli that detect and flush out arsenic to determine levels of the element in the waters of Puget Sound. If arsenic is present, we have planned to insert a reporter gene that, when synthesized, will turn the E. coli dark green. To make this vision a reality, we are using an arsR promoter, a dark green E. chromi reporter from the 2009 Cambridge team's project.
Arsenic Information
Arsenic is a chemical element (As) and the atomic number for Arsenic is 33. Arsenic contamination of groundwater is a problem is a problem that affects millions of the people across the world. The word Arsenic was borrowed from the Syriac word ܠܐ ܙܐܦܢܝܐ , meaning "yellow orpiment". It is also related to the Greek word arsenikon. During the Bronze Age arsenic was often included in bronze, which made alloy harder. Albert the Great is believed to have been the first person to isolate Arsenic. In the Victorian Era "arsenic" mixed with vinegar and chalk was eaten by women to "improve" their complexion. Arsenic was also rubbed onto the arms, legs and faces of women. In 1858, the accidental use of arsenic by a food staff led to the Bradford sweet poisoning, killing about 20 people.
[http://www.consumerreports.org/cro/consumer-reports-magazine-january-2012/arsenic-in-your-juice/index.htm Link to video about Arsenic in Apple Juice] File:Map.gif
Notebook
6/1-3/12
We attempted to transform E. Coli with test plasmids provided in our kit. Protocol:
1 Make sure set-up is complete.
2 Add 200 microliters Cacl2 Solution to each tube.
3 Harvest NEBlO cells: Scrape off the plate for eact tube Resuspend all the tubes
4 Add DNA to each tube: 5 microliters of "RFP Control" to control tube 2-5 microliters of other plasmids to labeled tubes
5 Incubate on ice for 5 minutes.
6 Place in hot water bath for 90 seconds.
7 Place tubes on ice for another minute.
8 Add 200 microliters of SOC media (pre-heated).
9 Label 3 plates, with appropiate drug.
10 Add 200 microliters of transformed cells to plate, spread evenly.
11Put plates in incubator.
Our results were not what we were hoping because the growth of the cells did not occur. The cells were competent, but either they did not take in the plasmids or they did not survive the transfers between heat and cold.
6/8/12
We
This first trial did not have our desired results.
Results/Conclusions
What did you achieve over the course of your semester?
Safety
What safety precautions did your team take? Did you take a safety training course? Were you supervised at all times in the lab?
Attributions
Who worked on what?
Human Practices
According to Department of Ecology: State of Washington"Organic and and inorganic arsenic were analyzed in eight fish and shellfish species to determine the appropriateness of placing five Puget Sound waterbodies on the 1998 303(d) list for exceeding EPA human health criteria in edible tissue. The waterbodies in question were Dyes Inlet, Port Washington Narrows, Sinclair Inlet, Port Orchard, and Eagle Harbor. The listings were based on total arsenic data. Results showed the listing criterion of 0.006 ug/g inorganic arsenic was exceeded in all clam samples analyzed. However, this appears to be due to natural conditions in Puget Sound. All crab and fish samples were at or below the listing criterion. It is therefore recommended that these waterbodies be taken off the 303(d) list for arsenic exceedances in edible tissue (12 listings in all)."
Fun!
Our teams favorite snacks consisted of candy, trail mix, and Pirate's Booty. Our team came up with many silly names including, but not limited to, "Dazzle Butters", "Avenging the Ginger", and "Team E.P.I.C". The name "Dazzle Butter" came out of no where and was love instantly. "Avenging the Ginger" is inspired by our redheaded team memeber, who despises this name. "Team E.P.I.C" was supposed to be a acronym for something that related to our team and iGEM, but after about 4 attempts that ended with silly disses toward Cambridge, we gave up and moved on to "Arsenic Avengers", inspired by the new movie- [http://www.imdb.com/title/tt0848228/ The Avengers ]<forum_subtle />