Small Phage
From 2013.igem.org
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Overview | Overview | ||
- | + | Winter | |
- | + | [[Team:BYU Provo/Notebook/SmallPhage/Springexp|Spring]] | |
- | + | Summer | |
- | + | Fall | |
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+ | '''add overview''' | ||
- | + | Description of our purpose and approaches | |
- | + | '''Pages that needs deleting''' | |
- | + | [[Spring]] [[Winter]] | |
- | ''' | + | |
+ | '''Things to figure out''' | ||
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+ | How to format table? | ||
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+ | How to format text besides default? | ||
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+ | Domain/URL? | ||
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+ | text alignment in table | ||
| style="width: 20%; background-color: transparent;"| | | style="width: 20%; background-color: transparent;"| | ||
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- We performed T7 Minor Capsid Protein PCR | - We performed T7 Minor Capsid Protein PCR | ||
: [[5.20 T7 Minor Capsid Protein PCR]] | : [[5.20 T7 Minor Capsid Protein PCR]] | ||
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+ | ===5/21/13=== | ||
+ | |||
+ | XL | ||
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+ | - started two 5mL E coli BL21 overnight at around 7:00pm | ||
+ | |||
+ | |||
+ | ===5/22/13=== | ||
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+ | - Continued with [[5.20 Mutagen Concentration Experiment|T7 Mutagen Concentration Test]] | ||
+ | |||
+ | - Continued with [[5.20 T7 Minor Capsid Protein PCR|T7 Minor Capsid Protein PCR ]] by running an agarose gel to confirm that we got the desired PCR product. | ||
==June== | ==June== |
Latest revision as of 15:06, 24 May 2013
Small Phage (Add formatting) | ||
Overview Winter Summer Fall |
add overview Description of our purpose and approaches Pages that needs deleting Things to figure out How to format table? How to format text besides default? Domain/URL? text alignment in table |
add picture |
Contents |
March
April
May
5/1/13
- Commencement of spring!!!
- Discussed goals and outlined plans for spring term
5/2/13
- Designed primers for amplifying and sequencing phage capsid protein
- Wrote emails inquiring mutagen (NG) and plasmid for in vitro assembly
5/3/13
- Performed agar test, focusing primarily on ×8
- Processed phage amplification
5/4/13
- Performed dilution series using stock 5.3 (-1 through -11)
- Started two 5mL overnights of BL21
5/5/13
- Spot test using stock 5.3 and its dilution series (from 5.4)
- Started liquid culture for purification team (at around noon)
- 1mL of BL21 overnight + 4mL of LB + 100μL -2 phage (received stock)
- Started 5.5 amplification from a plaque test
5/6/13
- Continued 5.3 T7 phage amplification/purification
- Performed liquid culture phage concentration test
5/7/13
- Started two 5mL of E coli BL21 overnight
- Designed procedure for applying mutagen and selecting for T7
5/8/13
- Went over procedure for applying mutagen and PCR with Dr. Grose
- Performed spot tests under 5.6 T7+ Liquid Culture Phage Concentration Test
- Started two 5mL BL21 overnights
- Learned how to create LB plates
5/9/13
- Practiced with ×6 and ×8 top agar
- Started 5.9 T7+ Liquid Culture Phage Concentration Test #2
- Discussed plans and schedule for next week.
5/20/13
LP, XL
- We performed T7 Mutagen Concentration Test
- We performed T7 Minor Capsid Protein PCR
5/21/13
XL
- started two 5mL E coli BL21 overnight at around 7:00pm
5/22/13
- Continued with T7 Mutagen Concentration Test
- Continued with T7 Minor Capsid Protein PCR by running an agarose gel to confirm that we got the desired PCR product.
June
July
August
September