Team:Stanford/Notebook/Lab Work/Week 4
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===Kairna's Notebook=== | ===Kairna's Notebook=== | ||
- | Goal: Left Laura to gel extract previous PCR product as I worked on the new PCR product. Today, | + | Goal: Left Laura to gel extract previous PCR product as I worked on the new PCR product. Today, must make and run a diagnostic gel, PCR clean up, then digest RSID 1 and RSID 2. <br/><br/> |
'''Make TAE''' <br/> | '''Make TAE''' <br/> | ||
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*1 g agarose + 50 mL TAE | *1 g agarose + 50 mL TAE | ||
*10 uL EtBr <br/> | *10 uL EtBr <br/> | ||
- | |||
Also, made Chris an 0.8% agarose gel (to repay him for yesterday). <br/><br/> | Also, made Chris an 0.8% agarose gel (to repay him for yesterday). <br/><br/> | ||
+ | |||
+ | |||
Revision as of 20:22, 22 July 2010
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7/19 Monday
Laura's Notebook
set up the following ligations from the gel extractions done by me, Karina, and Francisco on Friday, 7/14/10)
- Francisco ran and imaged diagnostic gel on Friday
Ligation Recipe | |
---|---|
dH2O | none |
vector (with terminators attached) | 5.0 uL |
insert (RFP or GFP) | 12.0 uL |
10X buffer | 2.0 uL |
T4 ligase | 1.0 uL |
- normally run for 10 minutes at room temperature, overnight this time (started at 11:30 am)
Nanodrop data (deemed unreliable based on 260/230, possibly due do residual EtBr contamination)
part | 260/280 | 260/230 | ng/uL |
vector/terminator | 1.77 | 0.03 | 19.1 |
RFP | 1.86 | 0.02 | 16.2 |
GFP | 1.83 | 0.02 | 14.8 |
Karina's Notebook
Goal: Laura will ligate GFP and RFP and ligate them to terminators. We received our RSID + RBS oligos in the mail, so I will work on the PCR. I first need to make freezer stock and working stock of oligos. Won't start PCR until after lunch because we'll leave them overnight with Chris' PCR reactions.
Make Tris-HCl
Need .01 L of 10mM Tris-HCl solution. So, add 15.76 mg Tris-HCl to 10 mL H20.
- Hard to weigh out 15.8 mg, so instead got to 18.3 mg.
- Determined that need to add this to 11.6 mL H20
Make Freezer Stock of Oligos
Want 100 uM solution of Tris-HCl solution
- Amount of Tris-HCl to add depends on how much of the oligo's we received.
amount (nmol) | mass (mg) | amount of Tris to add (uL) | |
RSID 1 + RBS Forward | 70.2 | 1.82 | 702 |
RSID 1 + RBS Reverse | 76.7 | 1.85 | 767 |
RSID 2 + RBS Forward | 81.1 | 2.22 | 811 |
RSID 2 + RBS Reverse | 83.5 | 2.09 | 835 |
Make Working Stock
Want a 10uM working stock solution
- 900 uL water + 100 uL Freezer Stock Solution
PCR Assembly
PCR Protocol calls for:
1.25 uL reverse primer
1.25 uL forward primer
DNA Template
50 uL PCR supermix
- For PCR Assembly, do not need DNA template. Also, add 4 times as much of each primer for PCR assembly.
Revised Recipe
5 uL Forward Primer
5 uL Reverse Primer
40 uL PCR Supermix
- we'll be using awesome PCR supermix- KEEP ON ICE
- Ran PCR with Chris, left running overnight
7/20 Tuesday
Laura's Notebook
helped Alex with preparation of competent cells
- see protocol: [http://openwetware.org/wiki/Stanford/BIOE44:Module_1:Day3 Preparing Electrocompetent Cells]
ran diagnostic gel for PCR-assembled DNA (Karina set up PCR rxns yesterday)
- order on gel:
- 100 bp ladder
- RSID1/RBS
- RSID2/RBS
Karina's Notebook
Goals: Run gel of PCR Assembly Product, gel extraction, digest, then run PCR clean up.
Make Gel
- Chris made me an 0.8% agarose gel
Load Gel
- added 10 uL loading dye directly into PCR tubes
- loaded 40 uL of each sample into wells
Gel Results
[insert picture here]
Analysis/Observations
Gel looked a little streaky to me, but we really only need the brightest bands (as circled). For next time:
- use 100 bp ladder (instead of 1 kb)
- Don't even bother with gel extraction after running a PCR. It is highly inefficient and a lot of DNA will be lost. Instead, run a a diagnostic gel to check that PCR assembly worked but then proceed to run a PCR cleanup and then digest.
Extraction
Extracted 1A, 1B, 2B, and 2C from the gel.
sample | tube mass (g) | mass w/getl (g) | gel mass (g) | volume of QG to add (uL) |
1A | 1.01 | 1.25 | .24 | 720 |
1B | 1.01 | 1.28 | .27 | 810 |
2B | 1.01 | 1.24 | .23 | 690 |
2C | 1.01 | 1.24 | .23 | 690 |
- extracted and incubated each of the samples separately. To combine, loaded 1A and 1B into one spin column and 2B and 2C into another. Loaded up to 800 uL, spun down, loaded, then spun again. Then continued to follow [http://molecool.wustl.edu/krolllab/Kroll_Lab_Protocols/Molecular%20Biology%20protocols/Cloning%20protocols%20folder/Gel%20extraction-Qiagen.pdf procedure].
PCR Assembly
Set up another PCR assembly of RSID 1 and RSID 2 so that we have samples that have not been gel extracted. Will let run overnight.
7/21 Wednesday
Laura's Notebook
today's digestions:
- RSID1, RSID2 (gel extracted from first PCR done by Karina)- digest with XbaI, PstI
- run overnight; started at 11:30am
- promoters within backbones (I0500-from Greg's box, and F2620-from Chris' box)- digest with SpeI, then PstI
- SpeI digest run for 3 hours, then heat killed 20 min. at 80oC, then PstI added overnight (to reduce enzyme competition for sites on the DNA, since recognition sequences are very close to each other)
Recipe:
component | amount (uL) |
DNA | 12.0 |
H2O | 26.0 |
10X NEB buffer #2 | 5.0 |
10 X BSA | 5.0 |
each enzyme | 1.0 (2.0 total) |
Kairna's Notebook
Goal: Left Laura to gel extract previous PCR product as I worked on the new PCR product. Today, must make and run a diagnostic gel, PCR clean up, then digest RSID 1 and RSID 2.
Make TAE
Need a 1 L solution; we have 50x TAE stock
- 20 mL 50x TAE + 980 mL H20
Make Gel
Want a 2% agarose gel because oligos are short (~220 bp).
- 1 g agarose + 50 mL TAE
- 10 uL EtBr
Also, made Chris an 0.8% agarose gel (to repay him for yesterday).