Small Phage
From 2013.igem.org
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{{TeamBYUProvo}} | {{TeamBYUProvo}} | ||
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+ | {| width="100%" | ||
+ | | colspan="3" | Small Phage (Add formatting) | ||
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+ | |- | ||
+ | | style="width: 20%; background-color: transparent;"| | ||
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+ | Overview | ||
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+ | Winter | ||
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+ | [[Team:BYU Provo/Notebook/SmallPhage/Springexp|Spring]] | ||
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+ | Summer | ||
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+ | Fall | ||
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+ | | style="width: 60%; background-color: transparent;"| | ||
+ | '''add overview''' | ||
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+ | Description of our purpose and approaches | ||
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+ | '''Pages that needs deleting''' | ||
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+ | [[Spring]] [[Winter]] | ||
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+ | '''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 | ||
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+ | | style="width: 20%; background-color: transparent;"| | ||
+ | '''add picture''' | ||
+ | |||
+ | |} | ||
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==March== | ==March== | ||
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===5/1/13=== | ===5/1/13=== | ||
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- Commencement of spring!!! | - Commencement of spring!!! | ||
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===5/2/13=== | ===5/2/13=== | ||
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- Designed primers for amplifying and sequencing phage capsid protein | - Designed primers for amplifying and sequencing phage capsid protein | ||
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===5/3/13=== | ===5/3/13=== | ||
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- Performed agar test, focusing primarily on ×8 | - Performed agar test, focusing primarily on ×8 | ||
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===5/4/13=== | ===5/4/13=== | ||
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- Performed dilution series using stock 5.3 (-1 through -11) | - Performed dilution series using stock 5.3 (-1 through -11) | ||
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===5/5/13=== | ===5/5/13=== | ||
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- Spot test using stock 5.3 and its dilution series (from 5.4) | - Spot test using stock 5.3 and its dilution series (from 5.4) | ||
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===5/6/13=== | ===5/6/13=== | ||
- | - Continued | + | - Continued [[5.3 T7 phage amplification/purification]] |
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- Performed liquid culture phage concentration test | - Performed liquid culture phage concentration test | ||
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: [[5.6 T7+ Liquid Culture Phage Concentration Test]] | : [[5.6 T7+ Liquid Culture Phage Concentration Test]] | ||
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+ | ===5/7/13=== | ||
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+ | - Started two 5mL of E coli BL21 overnight | ||
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+ | - Designed procedure for applying mutagen and selecting for T7 | ||
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+ | ===5/8/13=== | ||
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+ | - Went over procedure for applying mutagen and PCR with Dr. Grose | ||
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+ | - Performed spot tests under [[5.6 T7+ Liquid Culture Phage Concentration Test]] | ||
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+ | - Started two 5mL BL21 overnights | ||
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+ | - Learned how to create LB plates | ||
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+ | ===5/9/13=== | ||
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+ | - Practiced with ×6 and ×8 top agar | ||
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+ | : [[5.9 T7 selection method test #2]] | ||
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+ | - Started [[5.9 T7+ Liquid Culture Phage Concentration Test #2]] | ||
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+ | - Discussed plans and schedule for next week. | ||
===5/20/13=== | ===5/20/13=== | ||
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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=== | ||
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+ | XL | ||
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+ | - started two 5mL E coli BL21 overnight at around 7:00pm | ||
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+ | |||
+ | ===5/22/13=== | ||
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+ | - Continued with [[5.20 Mutagen Concentration Experiment|T7 Mutagen Concentration Test]] | ||
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+ | - 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