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Team:Leicester/Attributions
From 2012.igem.org
(Difference between revisions)
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<dt><h2>Christopher Morton</h2></dt> | <dt><h2>Christopher Morton</h2></dt> | ||
<dt>10th July: Plated out several of the CSE kits. </dt> | <dt>10th July: Plated out several of the CSE kits. </dt> | ||
| - | <dt>12th July: Photographed all of the CSE kits for recording the bacterial growth. | + | <dt>12th July: Photographed all of the CSE kits for recording the bacterial growth. Helped with the testing of acetone on polystyrene. Made the 1st plate of dissolved polystrene embedded in the Luria agar as a test to see if the method worked. Made up dilutions of acetone and used methanol to see their effects on polystyrene. </dt> |
| - | + | ||
| - | + | ||
| - | + | ||
<dt>13th July: Learnt how to use the grinder in an attempt to grind the polystyrene. </dt> | <dt>13th July: Learnt how to use the grinder in an attempt to grind the polystyrene. </dt> | ||
| - | <dt>16th July: Prepared the minimal media. | + | <dt>16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down. </dt> |
| - | + | ||
| - | + | ||
<dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''. </dt> | <dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''. </dt> | ||
| - | <dt>19th July: Shaved EPS to try and recreate our suspension. | + | <dt>19th July: Shaved EPS to try and recreate our suspension. Plated up some more by sprinkling the polystyrene "sugar" on top of the agar.</dt> |
| - | + | ||
<dt>23rd July: Went around town looking on the sponsorship drive. </dt> | <dt>23rd July: Went around town looking on the sponsorship drive. </dt> | ||
| - | <dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. | + | <dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. Helped to produce the corning tubes for the liquid suspension of ''Pseudomonas sp''. </dt> |
| - | + | ||
<dt>1st August: Produced the 15ml corning tubes for the suspension of ''Pseudomonas sp'' in rich media. </dt> | <dt>1st August: Produced the 15ml corning tubes for the suspension of ''Pseudomonas sp'' in rich media. </dt> | ||
<dt>3rd August: Made the buffers B1 and B2 for the DNA extraction. </dt> | <dt>3rd August: Made the buffers B1 and B2 for the DNA extraction. </dt> | ||
| - | <dt>6th August - 9th August: Genomic DNA Extraction with QIAGEN Maxi prep, Take one and two </dt> | + | <dt>6th August - 9th August: Genomic DNA Extraction with QIAGEN Maxi prep, Take one and two.</dt> |
<dt>10th August: Videod a lot of the Rockethub video, to almost have the video complete. </dt> | <dt>10th August: Videod a lot of the Rockethub video, to almost have the video complete. </dt> | ||
| - | <dt>13th August: Worked on the Rockethub site, making it ready to be published. | + | <dt>13th August: Worked on the Rockethub site, making it ready to be published. Prepared overnight cultures for the next Genomic tip.</dt> |
| - | + | ||
<dt>14th August: Worked on the second Genomic extraction, prepared the samples for the gel, worked out how to adapt the tips to allow for pressure to be applied. </dt> | <dt>14th August: Worked on the second Genomic extraction, prepared the samples for the gel, worked out how to adapt the tips to allow for pressure to be applied. </dt> | ||
<dt>15rd August: loaded, ran and photographed the gel. started the preperatation for the next tip, made the gel for tomorrow </dt> | <dt>15rd August: loaded, ran and photographed the gel. started the preperatation for the next tip, made the gel for tomorrow </dt> | ||
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<dt><h2>Anthony Cox</h2></dt> | <dt><h2>Anthony Cox</h2></dt> | ||
<dt>10th July: Plated out several of the CSE kits. </dt> | <dt>10th July: Plated out several of the CSE kits. </dt> | ||
| - | <dt>13th July: Used the mortar and pestle to try and grind the polystyrene. | + | <dt>13th July: Used the mortar and pestle to try and grind the polystyrene. Learnt how to use the grinder in an attempt to grind the polystyrene. </dt> |
| - | + | <dt>16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down. </dt> | |
| - | <dt>16th July: Prepared the minimal media. | + | |
| - | + | ||
| - | + | ||
<dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''. </dt> | <dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''. </dt> | ||
<dt>19th July: Plated up some more by sprinkling the polystyrene "sugar" on top of the agar. </dt> | <dt>19th July: Plated up some more by sprinkling the polystyrene "sugar" on top of the agar. </dt> | ||
| Line 88: | Line 77: | ||
<dl> | <dl> | ||
<dt><h2>Philip Higgs</h2></dt> | <dt><h2>Philip Higgs</h2></dt> | ||
| - | <dt>12th July: Photographed all of the CSE kits for recording the bacterial growth. | + | <dt>12th July: Photographed all of the CSE kits for recording the bacterial growth. Helped with the testing of acetone on polystyrene. Made the 1st plate of dissolved polystrene embedded in the Luria agar as a test to see if the method worked. Made up dilutions of acetone and used methanol to see their effects on polystyrene.</dt> |
| - | + | <dt>13th July: Used the mortar and pestle to try and grind the polystyrene. Learnt how to use the grinder in an attempt to grind the polystyrene. </dt> | |
| - | + | <dt>16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down. </dt> | |
| - | + | ||
| - | <dt>13th July: Used the mortar and pestle to try and grind the polystyrene. | + | |
| - | + | ||
| - | <dt>16th July: Prepared the minimal media. | + | |
| - | + | ||
| - | + | ||
<dt>19th July: Spent almost the whole day researching methods of transport to Amsterdam and hotels for the stay at the Jamboree to find the best deal both pricewise and comfort. </dt> | <dt>19th July: Spent almost the whole day researching methods of transport to Amsterdam and hotels for the stay at the Jamboree to find the best deal both pricewise and comfort. </dt> | ||
<dt>20th July: Produced the nutrient broth for the liquid suspension plates. </dt> | <dt>20th July: Produced the nutrient broth for the liquid suspension plates. </dt> | ||
<dt>23rd July: Went around town looking on the sponsorship drive.</dt> | <dt>23rd July: Went around town looking on the sponsorship drive.</dt> | ||
| - | <dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. | + | <dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. Helped to produce the corning tubes for the liquid suspension of ''Pseudomonas sp''. </dt> |
| - | + | <dt>1st August: Sorted out all the information needed to pick the correct DNA extraction kit. Produced the 15ml corning tubes for the suspension of ''Pseudomonas sp'' in rich media. </dt> | |
| - | <dt>1st August: Sorted out all the information needed to pick the correct DNA extraction kit. | + | |
| - | + | ||
<dt>2nd August: Innoculated tshe 15ml corning tube with ''E. coli'' for the DNA extraction test. </dt> | <dt>2nd August: Innoculated tshe 15ml corning tube with ''E. coli'' for the DNA extraction test. </dt> | ||
<dt>3rd August: Did the CFU colonies and dilutions test with ''E. coli''. </dt> | <dt>3rd August: Did the CFU colonies and dilutions test with ''E. coli''. </dt> | ||
| - | <dt>6th August: Altered the protocol for the dilutions experiment. | + | <dt>6th August: Altered the protocol for the dilutions experiment. Used the spectrophotometer to give the DNA digest the starting value. Innoculated the 3ml of luria broth for the final ''E. coli'' test. </dt> |
| - | + | ||
| - | + | ||
<dt>7th August: Worked for the whole day doing spectrophotometry to finally get the experiment right with a good protocol. </dt> | <dt>7th August: Worked for the whole day doing spectrophotometry to finally get the experiment right with a good protocol. </dt> | ||
<dt>8th August: Repeated the CFU colonies and dilutions test with ''E. coli''. </dt> | <dt>8th August: Repeated the CFU colonies and dilutions test with ''E. coli''. </dt> | ||
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<dt><h2>William Harrison</h2></dt> | <dt><h2>William Harrison</h2></dt> | ||
<dt>10th July: Wrote the wiki entries for all of the plating and details.</dt> | <dt>10th July: Wrote the wiki entries for all of the plating and details.</dt> | ||
| - | <dt>16th July: Prepared the minimal media. | + | <dt>16th July: Prepared the minimal media. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down. </dt> |
| - | + | ||
<dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''.</dt> | <dt>18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''.</dt> | ||
| - | <dt>19th July: Shaved EPS to try and recreate our suspension. | + | <dt>19th July: Shaved EPS to try and recreate our suspension. Plated up some more by sprinkling the polystyrene "sugar" on top of the agar. </dt> |
| - | + | ||
<dt>20th July: Produced the nutrient broth for the liquid suspension plates. </dt> | <dt>20th July: Produced the nutrient broth for the liquid suspension plates. </dt> | ||
| - | <dt>23rd July: Filled out the COSHH form. | + | <dt>23rd July: Filled out the COSHH form. Went around town looking on the sponsorship drive.</dt> |
| - | + | <dt>24th July: Filled out new COSHH form. Called the potential sponsors found on the 23rd.</dt> | |
| - | <dt>24th July: Filled out new COSHH form. | + | |
| - | + | ||
<dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. </dt> | <dt>31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. </dt> | ||
<dt>2nd August: Found all the ingredients needed for the experiments on the 3rd. </dt> | <dt>2nd August: Found all the ingredients needed for the experiments on the 3rd. </dt> | ||
| Line 143: | Line 118: | ||
<dt>9th July: Determined the protocol for plating out all the CSE kits coming back.</dt> | <dt>9th July: Determined the protocol for plating out all the CSE kits coming back.</dt> | ||
<dt>10th July: Plated out several of the CSE kits. </dt> | <dt>10th July: Plated out several of the CSE kits. </dt> | ||
| - | <dt>12th July: Helped with the testing of acetone on polystyrene. | + | <dt>12th July: Helped with the testing of acetone on polystyrene. Made up dilutions of acetone and used methanol to see their effects on polystyrene.</dt> |
| - | + | ||
<dt>19th July: Made the method and tested it worked to sprinkle the polystyrene "sugar" on top of the agar.</dt> | <dt>19th July: Made the method and tested it worked to sprinkle the polystyrene "sugar" on top of the agar.</dt> | ||
<dt>3rd August: Made the buffers B1 and B2 for the DNA extraction. </dt> | <dt>3rd August: Made the buffers B1 and B2 for the DNA extraction. </dt> | ||
Revision as of 10:53, 3 September 2012
Attributions
Each team must clearly attribute work done by the team on this page. They must distinguish work done by the team from work done by others, including the host labs, advisors, instructors, graduate students, and postgraduate masters students.
Christopher Morton
- 10th July: Plated out several of the CSE kits.
- 12th July: Photographed all of the CSE kits for recording the bacterial growth. Helped with the testing of acetone on polystyrene. Made the 1st plate of dissolved polystrene embedded in the Luria agar as a test to see if the method worked. Made up dilutions of acetone and used methanol to see their effects on polystyrene.
- 13th July: Learnt how to use the grinder in an attempt to grind the polystyrene.
- 16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down.
- 18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''.
- 19th July: Shaved EPS to try and recreate our suspension. Plated up some more by sprinkling the polystyrene "sugar" on top of the agar.
- 23rd July: Went around town looking on the sponsorship drive.
- 31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. Helped to produce the corning tubes for the liquid suspension of ''Pseudomonas sp''.
- 1st August: Produced the 15ml corning tubes for the suspension of ''Pseudomonas sp'' in rich media.
- 3rd August: Made the buffers B1 and B2 for the DNA extraction.
- 6th August - 9th August: Genomic DNA Extraction with QIAGEN Maxi prep, Take one and two.
- 10th August: Videod a lot of the Rockethub video, to almost have the video complete.
- 13th August: Worked on the Rockethub site, making it ready to be published. Prepared overnight cultures for the next Genomic tip.
- 14th August: Worked on the second Genomic extraction, prepared the samples for the gel, worked out how to adapt the tips to allow for pressure to be applied.
- 15rd August: loaded, ran and photographed the gel. started the preperatation for the next tip, made the gel for tomorrow
Anthony Cox
- 10th July: Plated out several of the CSE kits.
- 13th July: Used the mortar and pestle to try and grind the polystyrene. Learnt how to use the grinder in an attempt to grind the polystyrene.
- 16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down.
- 18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''.
- 19th July: Plated up some more by sprinkling the polystyrene "sugar" on top of the agar.
- 1st August: Made the protocol for the DNA hybridization.
- 2nd August: Made the protocol for the DNA extraction test, as well as the growth curves by diluting a broth.
- 3rd August: Did the CFU colonies and dilutions test with ''E. coli''.
- 6th August: Altered the protocol for the dilutions experiment.
- 7th August: Worked for the whole day doing spectrophotometry to finally get the experiment right with a good protocol.
- 8th August: Repeated the CFU colonies and dilutions test with ''E. coli''.
- 9th August: Counted colonies from the successful test, and then produced a growth curve for future reference.
- 14th August: Ran the doubling experiment for ''Pseudomonas'' to give a basic time to work with in the dilutions experiment.
Philip Higgs
- 12th July: Photographed all of the CSE kits for recording the bacterial growth. Helped with the testing of acetone on polystyrene. Made the 1st plate of dissolved polystrene embedded in the Luria agar as a test to see if the method worked. Made up dilutions of acetone and used methanol to see their effects on polystyrene.
- 13th July: Used the mortar and pestle to try and grind the polystyrene. Learnt how to use the grinder in an attempt to grind the polystyrene.
- 16th July: Prepared the minimal media. Worked with the frozen polystyrene (-80oC) in an attempt to grind it down. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down.
- 19th July: Spent almost the whole day researching methods of transport to Amsterdam and hotels for the stay at the Jamboree to find the best deal both pricewise and comfort.
- 20th July: Produced the nutrient broth for the liquid suspension plates.
- 23rd July: Went around town looking on the sponsorship drive.
- 31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates. Helped to produce the corning tubes for the liquid suspension of ''Pseudomonas sp''.
- 1st August: Sorted out all the information needed to pick the correct DNA extraction kit. Produced the 15ml corning tubes for the suspension of ''Pseudomonas sp'' in rich media.
- 2nd August: Innoculated tshe 15ml corning tube with ''E. coli'' for the DNA extraction test.
- 3rd August: Did the CFU colonies and dilutions test with ''E. coli''.
- 6th August: Altered the protocol for the dilutions experiment. Used the spectrophotometer to give the DNA digest the starting value. Innoculated the 3ml of luria broth for the final ''E. coli'' test.
- 7th August: Worked for the whole day doing spectrophotometry to finally get the experiment right with a good protocol.
- 8th August: Repeated the CFU colonies and dilutions test with ''E. coli''.
- 9th August: Counted colonies from the successful test.
- 10th August: Videod a lot of the Rockethub video, to almost have the video complete.
- 13th August: Plated out all the CSE kits onto 5% polystyrene on minimal agar.
- 14th August: Ran the doubling experiment for ''Pseudomonas'' to give a basic time to work with in the dilutions experiment.
William Harrison
- 10th July: Wrote the wiki entries for all of the plating and details.
- 16th July: Prepared the minimal media. Worked with the liquid nitrogen in a further attempt to grind the polystyrene down.
- 18th July: Finished making the control, 5% and 10% polystyrene agar plates and took them to the other lab to be plated with ''Pseudomonas''.
- 19th July: Shaved EPS to try and recreate our suspension. Plated up some more by sprinkling the polystyrene "sugar" on top of the agar.
- 20th July: Produced the nutrient broth for the liquid suspension plates.
- 23rd July: Filled out the COSHH form. Went around town looking on the sponsorship drive.
- 24th July: Filled out new COSHH form. Called the potential sponsors found on the 23rd.
- 31st July: Helped to produce the minimal media plates for the ''E. coli'' and ''Pseudomonas. sp'' as control plates.
- 2nd August: Found all the ingredients needed for the experiments on the 3rd.
- 3rd August: Worked around with other labs to find all the ingredients for the buffers B1 and B2 for the DNA extraction test.
- 6th August - 10th August: Genomic DNA Extraction with QIAGEN Maxi prep, Take one and two
- 14th August: Worked on the second Genomic extraction, prepared the samples for the gel, prepared the agarose and made the gel ready
- 15rd August: Nano drop spectrophotometry, started the preparation for the next tip
Luke Thompson
- 9th July: Determined the protocol for plating out all the CSE kits coming back.
- 10th July: Plated out several of the CSE kits.
- 12th July: Helped with the testing of acetone on polystyrene. Made up dilutions of acetone and used methanol to see their effects on polystyrene.
- 19th July: Made the method and tested it worked to sprinkle the polystyrene "sugar" on top of the agar.
- 3rd August: Made the buffers B1 and B2 for the DNA extraction.
- 6th August - 10th August Genomic DNA Extraction with QIAGEN Maxi prep, Take one and two
Emily Halsey
- 12th July: Photographed all of the CSE kits for recording the bacterial growth.
Nathan Hanna
- 16th July: Wrote and edited the Rockethub script.
- 17th-31st July: Did all the editing/stitching together of the Rockethub video, as it was produced.
- 1st August: Tested the cooling for our hybridization in the DNA extraction and isolation processes.
- 3rd August: Did the CFU colonies and dilutions test with ''E. coli''.
- 10th August: Videod a lot of the Rockethub video, to almost have the video complete.
- 14th August: Ran the doubling experiment for ''Pseudomonas'' to give a basic time to work with in the dilutions experiment.
- 20th August: Corrected the entire wiki, spelling errors, grammatical errors and punctuation errors.
Reema Naran
- 10th July: Plated out several of the CSE kits.
Mohammed Idres
- 10th July: Plated out several of the CSE kits.
Dr Badge
- 14th August: Worked on the second Genomic extraction, prepared the samples for the gel, worked out how to adapt the tips to allow for pressure to be applied.
Dr Dalgleish
Dr Ketley
Dr Bayliss
Sue Hardy (Lab technician)
- 29th July: Plated up some ''E. coli'' for the team to use.
- 5th August: Produced the overnight cultures of ''E. coli'' for the team to use.
Alex (researcher)
Carlo (researcher)
- 16th July: Brought the team liquid nitrogen and showed us how to use it safely.
Pseudomonas researcher - Jaspreet Sahota
- 18th July: Plated out the control, 5% and 10% polystyrene plates with 5 strains of ''Pseudomonas''.
