SBB10Ntbk-AmyKristofferson

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BioE140L 2010 Homepage
My Project Page

Contents

3/20/10: Success!

  • My sequencing results are perfect. The part sbb22 was a success!

3/17/10: Submitted sbb22 for Sequencing

  • I logged my samples into clotho and loaded sbb22-1 and sbb22-2 for sequencing.

3/15/10

sbb22 Wetlab notes: Mapping attempt #2

  • I mapped my plasmids again and got the following analytical gel:

Image:WJH_gels_031510.jpg
My lanes are as follows:
6. sbb22-1
7. sbb22-2
8. sbb22-3
9. sbb22-4

I'm going to have 1 and 2 sequenced, since they both appear to have a band around 600bp. There are two bands between 2000 and 3000bp, which is probably due to an incomplete digestion.

sbb36 Wetlab notes: Miniprep, Mapping, and Failure

  • The GSI's picked colonies for me, so today I performed a mini prep. I labeled the tubes sbb36 plasmid 1-4, where the numbers correspond to the well I removed the cells from. Only tubes 1 and 3 produced a pellet.
  • I also mapped the plasmids. Sbb36-1 is in lane 2 and sbb36-3 is in lane 3. Since nothing substantial turned up, I'm not going to sequence any plasmids for this part and assume that the project failed. Prof Anderson will redo it over Spring Break.

Image:Jing_gel2.jpg

3/10/10

sbb22 Wetlab notes: Miniprep and unsuccessful Mapping

  • The GSI's picked colonies for me, so today I performed a mini prep. I labeled the tubes sbb22 plasmid 1-4, where the numbers correspond to the well I removed the cells from. There could be complications though, because the media was contaminated. Along with several fairly large, translucent white colonies (there was only one red colony), there were a ton of tiny white colonies- the contaminent.
  • I also mapped the plasmids.

The four lanes on the right are of my part. My part should be 603bp long, but there's no band of that length in any of my lanes. If the plasmid had just closed on itself, I would only expect a band at 2170bp. It appears that this was the case; that I was just unlucky enough to choose four colonies that picked up plasmids that didn't contain my part. However, I'm going to map my mini-prepped plasmids again to make sure that I just didn't make a mistake when I digested them when prepping for the analytical gel.

Image:Mb031010.jpg

sbb36 Wetlab notes: Ligation and Transformation

  • Ligation of digest product and pre-digested pBca1256-Bca1144(instead of pBca9523- Bca1144, which I originally said I would use in my construction file)
  • Transformation into strain DH10B

3/8/10

sbb22 Wetlab notes: Ligation and Transformation

sbb36 Wetlab notes: Digest

Eco/Bam Transfer
(I amended this protocol so I could digest today and then ligate and transform on Wednesday)

  • Set up the digest:
For BBb transfers:
6 uL ddH2O (changed from 7.5uL)
1 uL NEB2+ATP Buffer
0.5uL EcoRI
0.5uL BamHI
2 uL miniprepped plasmid: pBca9145-jtk2642 (changed from 0.5uL)
  • Incubate at 37 degrees on the thermocycler for 1hr
  • Perform Zymo clean-up. Now I should have purified insert and old plasmid DNA.

Note: a preparative gel isn't necessary to separate the insert from the original vector, because I will be able to select for the bacteria with the new vector by plating on spec, since the new vector has a specR gene, while the old vector does not. I labeled the tube "sbb36 Digest AK" and put it in Box A.

And then next time...

  • Add 0.5uL of predigest vector and 0.5uL of T4 DNA ligase
  • Incubate 30 min. at room temp, transform, rescue, plate.

3/3/10

sbb22 Wetlab notes: Successful SOEing PCR and Eco/Bam Digest

  • Ran an analytical gel of two PCR products

Image:3-3-10-gel.png
Lane 2: sbb22 H2O
Lane 3: sbb22 DMSO
Both PCR products contained a band around 600bp, but the band in lane 2 was darker, so I'm going to use "sbb22 H2O" to continue on with my project. I labeled it "sbb22 H2O AK" and put it in box A. I threw out the "sbb22 DMSO" product.

  • Performed a Zymo Cleanup of products while waiting for results.
  • Performed a Eco/Bam digest on my "sbb22 H2O" PCR product using this protocol.
  • Ran a preparative gel of digest, cut out higher band and melted gel in AB buffer.

Image:Ak3-3-10.png
My digest is in lane 2.

3/1/10

sbb22 Wetlab notes: Trying out alternative SOEing PCR techniques

I'm going to redo the SOEing PCR (using oligos gh1000F/ak11R on A+B+C template) using the 2K45 PCR program, since my first attempt with 55 failed. I'll set up one tube following the original protocol, and then another one with 3.3 uL of DMSO substituted for the usual 3.3uL of ddH2O.


I labeled the PCR tubes "sbb22 H2O" and "sbb22 DMSO."

2/24/10

sbb22 Wetlab Notes: SOEing PCR and Analytical Gel

  • PCR gh1000F/ak11R on A+B+C using this protocol and 55 PCR.
  • Ran analytical gel to verify that desired PCR product was created. (Protocol: add 3uL PCR product and 7uL of loading buffer)

Image:MN022410.png
My PCR product was labeled sbb22 and was in the fourth lane from the left. The PCR product should have been 619bp, but all the bands that showed up were under 500 bps.

  • While waiting for the gel, I performed a Zymo clean-up to remove dNTPs, Expand Polymerase, and oligos. What's left: the <500bp PCR product, A, B, C. DNA labeled "sbb22, final PCR product, AK" and placed in Box A. (3-3-10: I'm not using this PCR product, so I threw it out)

sbb22 Protocol Update

Next few steps (after performing a successful SOEing PCR)

  • Eco/Bam Digest of PCR product (vector has already been digested)
  • Run a preparative gel to separate digested product from A, B, and C and to ensure product was correctly digested
  • Cut out digested product and perform a Gel purification

2/22/10

sbb22 Wetlab Notes: Preparative Gel for PCR product A,B,C

Mixed 6uL of each PCR product with 4uL of loading buffer and ran the gel.

Image: AK 02 22 10.jpg Image:Generuler1kbplus.jpg
My PCR products A, B, and C were in lanes 2, 3, and 4.

I cut out the bottom bands (the upper band is most likely template DNA), performed a small fragment Zymo Cleanup, and stored the eluted DNA in Box A.

2/17/10

New sbb22 Construction File

Construction of FokI- basic part	
 PCR gh1000F/gh1001R on BBa_K243001   (261 bp, gp = A)
 PCR gh1001F/gh1003R on BBa_K243001   (264 bp, gp = B)
 PCR gh1003F/ak11R     Registry part BBa_K243001            (141 bp, gp = C)
 ---------------------------------------------------
 PCR gh1000F/ak11R on A+B+C           (619bp, EcoRI/BamHI)
 Digest pBjk2741-Bca1144              (EcoRI/BamHI, 910+2170, L)
 Product is pBjk2741-sbb22   {<FokI->}
 ---------------------------------------------------
 gh1000F  Forward for part <FokI-!    ccagtGAATTCatgAGATCTCAGCTGGTTaaatctgaactggaggag
 gh1001F  Making internal mutation 1+2 cgttggttccccgatcgattatggcgttatcgtggAcacaaaagc
 gh1001R  Making internal mutation 1+2 cgccataatcgatcggggaaccaacggtataaatggcaccGTctggtttac
 gh1003F  Making internal mutation 3   ccatatcaccaatTgcaatggggcagtgctgag
 gh1003R  Making internal mutation 3   ccattgcAattggtgatatgg
 ak11R    Reverse BamHI for FokI- CTGATggatccaaaattgatctcgccattg

SOEing Protocol for sbb22

  • Set up PCR reactions according to your construction file as normal 33uL reactions as described in Cloning by PCR
  • For each PCR, load 6uL of PCR product premixed with 4uL of loading buffer in a single well of a 1% agarose gel
  • Cut out the bands, put them into a single 1.5mL microcentrifuge tube
  • Add 650uL of ADB Buffer
  • Proceed with the Zymo Gel Purification procedure
  • Elute the DNA in 50uL of water
  • Set up your second round of PCR as a normal 33uL reaction using the eluted mixture of fragments as template

sbb22 Wetlab notes: PCR of A,B,C off of template

Prepared oligos and set up three PCR tubes using this protocol. The PCR tubes were labeled A, B, and C and placed in Box A.

2/8/10: Construction Files for my parts

sbb22

Construction of FokI- basic part	
 PCR ak10F/ak20R     Registry part BBa_K243001            (230 bp, gp = A)
 PCR ak20F/ak30R     Registry part BBa_K243001            (71 bp, gp = B)
 PCR ak30F/ak40R     Registry part BBa_K243001            (245 bp, gp = C)
 PCR ak40F/ak11R     Registry part BBa_K243001            (135 bp, gp = D)
 ---------------------------------------------------
 PCR ak10F/ak11R on A+B+C+D           (619bp, EcoRI/BamHI)
 Digest pBjk2741-Bca1144              (EcoRI/BamHI, 910+2170, L)
 Product is pBjk2741-Bak1234  {<FokI->}
 ---------------------------------------------------
 ak10F  Forward EcoRI for FokI-      CCATAgaattcCAGagatctCAGCTGGTTaaatctgaactggaggagaa 
 ak20F  Base substitution 1  gtaaaccagACggtgccatt
 ak20R  Base substitution 1  aatggcaccGTctggtttac
 ak30F  Base substitution 2  cgttatcgtggAcacaaaagcg
 ak30R	Base substitution 2  cgcttttgtgTccacgataacgc
 ak40F  Base substitution 3  caccaatTgcaatggggcag
 ak40R  Base substitution 3  ctgccccattgcAattggtg
 ak11R Reverse BamHI for FokI-  CTGATggatccaaaattgatctcgccattg


sbb36

Construction of ColE2 Basic Part 
 Digest pBca9145-jtk2642                          (EcoRI/BamHI, 2057+485, S)
 Sub into pBca9523- Bca1144                        (EcoRI/BamHI, 2472+918, L)
 Product is pBca9523-jtk2642  {ColE2 ori med}
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