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From 2010.igem.org

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	|align="center"|ASB0045 780		|align="center"|ASB0045 780
	|}		|}
		+
		+	----
		+	==Nina==
		+
		+	===concentration measurement===
		+
		+	I measured the concentration of the gel cleaned up samples from yesterday by spectrophotometry.
		+
		+	[[Image:Aq16.jpg]]
		+
		+	===Ligation===
		+
		+	I ligated the gel cleaned samples.
		+
		+	[[Image:Aq17.jpg]]
		+
		+	===Transformation===
		+
		+	I transformed the ligation samples into nine BL21 tubes each with 100 ul cells. I added 6 ul of the ligations to the cells and I thawed the tubes in the first step in 15 min.
		+
		+	I hope this will save some time since I am skipping the transformation into Top 10 cells. We don't have much time left of the competition therefore I hope this will work.
		+
		+
		+
		+
		+	== Mimmi ==
		+
		+	=== Home page design ===
		+
		+	*Bacteria figures for each link...
		+	**saftey
		+	**Sponsors
		+	**Project
		+	**Planning
		+	**News
		+	**Team
		+	**Modelling
		+	**Notebook
		+	**Protocols
		+
		+	*to do (?):
		+	**Results
		+	**BioBricks
		+	**Assemblies
		+
		+
		+
		+	=== SOD - growth curve ===
		+	- ON culture
		+
		+	*SOD.his
		+	*LMWP.SOD.his
		+	*TAT.SOD.his
		+	*Tra10.SOD.his
		+
		+
		+	*3ml Amp<sub>100</sub> + toothpick of glycerol stock
		+
		+	{{Stockholm/Footer}}

---

Latest revision as of 11:10, 26 October 2010

Contents 1 Andreas 1.1 Plasmid prep 1.2 Sequencing 2 Nina 2.1 concentration measurement 2.2 Ligation 2.3 Transformation 3 Mimmi 3.1 Home page design 3.2 SOD - growth curve

Andreas

Plasmid prep

From 12/10 ON cultures

DNA concentration
Sample	Conc [ng/μl]	A260/A280
pSB1C3.IgGp	237.9	1.89
pSB1C3.bFGF	210.3	1.91
pSB1C3.ProtA	173.6	1.89
pSB1C3.yCCS	229.2	1.91
pSB1C3.SOD	193.0	1.87

Sequencing

• 15 μl plasmid DNA; 1.5 μl primer (VR)

DNA concentration
Sample	Label	Sequence code
pSB1C3.IgGp	pSB1C3.IgGp_VR	ASB0045 776
pSB1C3.bFGF	pSB1C3.bFGF_VR	ASB0045 777
pSB1C3.ProtA	pSB1C3.ProtA_VR	ASB0045 778
pSB1C3.yCCS	pSB1C3.yCCS_VR	ASB0045 779
pSB1C3.SOD	pSB1C3.SOD_VR	ASB0045 780

---

Nina

concentration measurement

I measured the concentration of the gel cleaned up samples from yesterday by spectrophotometry.

Ligation

I ligated the gel cleaned samples.

Transformation

I transformed the ligation samples into nine BL21 tubes each with 100 ul cells. I added 6 ul of the ligations to the cells and I thawed the tubes in the first step in 15 min.

I hope this will save some time since I am skipping the transformation into Top 10 cells. We don't have much time left of the competition therefore I hope this will work.

Mimmi

Home page design

• Bacteria figures for each link...
  • saftey
  • Sponsors
  • Project
  • Planning
  • News
  • Team
  • Modelling
  • Notebook
  • Protocols

• to do (?):
  • Results
  • BioBricks
  • Assemblies

SOD - growth curve

- ON culture

• SOD.his
• LMWP.SOD.his
• TAT.SOD.his
• Tra10.SOD.his

• 3ml Amp₁₀₀ + toothpick of glycerol stock