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	Incubated at 37C for 1.5hrs.		Incubated at 37C for 1.5hrs.
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		+	==Week of May 17th==
		+
		+	===May 13, 2014===
		+	Figured out that we didn’t want to use the promoter vectors that I digested. We tried using pIG91 from the freezer, but the RD gel did not show any DNA present.
		+	Also did plasmid mini-preps according to the Sigma-Aldrich kit, for new pIG91.
		+
		+	===May 15, 2014===
		+	Assisted in setting up new RD of pIG91.
		+	Assisted Nano-dropping the recently purified pIG91 plasmisds, all concentrations were approximately 100ng/ul.
		+	Assisted in setting up ligation of digested pIG91 (treated with CIP), with the digested Bla. Both were digested using SpeI HF and XbaI. This is so that we can then have our part in the iGEM registry plasmid to allow for quick and easy future cloning.

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Revision as of 21:25, 30 June 2014

BYU 2014 Notebook Edit May June

Home Team Official Team Profile Project Parts Modeling Notebook Safety Attributions

Contents 1 Week of May 10th 1.1 May 6, 2014 1.2 May 8, 2014 1.3 May 9, 2014 1.4 May 10, 2014 2 Week of May 17th 2.1 May 13, 2014 2.2 May 15, 2014

Week of May 10th

May 6, 2014

Nano-dropped the Promoter plasmids that were recently purified. Almost all of the plasmids were over 100ng/ul concentration.

May 8, 2014

Set up PCR to amplify Bla gene. Used Q5 polymerase and Q5 protocol.

• Q5 PCR
• 24.5 ul ddH20
• 10 ul Q5 Buffer
• 10 ul Q5 Enhancer
• 1 ul Bla forward primer BI374
• 1 ul Bla reverse primer BI375
• 1ul dNTP’s
• 1ul Template psB1A3 (resuspended with 10ul ddH20 from iGEM 2013 kit plate 5, well 1G)
• 0.5ul Q5

May 9, 2014

Ran a gel to check PCR products. Looks great! Did PCR-up of PCR product using Gen-Elute Kit:

1. Add 0.5mL column prep solution to column, spin at 12000 RPM 1 min. Discard eluate after 1 min.
2. Transfer PCR reaction mix into the tube
3. Add (5x’s volume) of binding solution to 1 volutm of PCR reaction and mix, 250ul
4. Add to column, centrifuge at max speed for 1 min
5. After 1 min discared eluate, but retain collection tube
6. Add 0.5 ml of diluted Wash Solution to the column, centrifuge at max speed for 1 minute
7. After 1 minute, discard the eluate, replace the column back in the collection tube. Centrifuge an additional 2 minutes to dry.
8. Place the column in a clean tube. Add 50ul elution buffer, wait 1 min. Spin max speed 1 min. Remove column, voila!

Ran restriction digests on vectors and insert. Chose the IGEM plasmids containing a strong, and medium-strong promoter strength respectively)

May 10, 2014

RD Protocol (repeated for each of the three samples)

• 14ul ddH20
• 5ul NEB Buffer 4
• 0.5 ul 100x BSA
• 30 ul DNA sample---(1 each of BBa_J23102, BBa_J23118, and PCR amplified Bla gene)
• 1.5 ul each of SpeI HF, and XbaI

Incubated at 37C for 1.5hrs.

Week of May 17th

May 13, 2014

Figured out that we didn’t want to use the promoter vectors that I digested. We tried using pIG91 from the freezer, but the RD gel did not show any DNA present. Also did plasmid mini-preps according to the Sigma-Aldrich kit, for new pIG91.

May 15, 2014

Assisted in setting up new RD of pIG91. Assisted Nano-dropping the recently purified pIG91 plasmisds, all concentrations were approximately 100ng/ul. Assisted in setting up ligation of digested pIG91 (treated with CIP), with the digested Bla. Both were digested using SpeI HF and XbaI. This is so that we can then have our part in the iGEM registry plasmid to allow for quick and easy future cloning.