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Revision as of 11:01, 4 October 2010 (view source) AndreasConstantinou (Talk | contribs) (→Assembly of His⋅SOD&sdotcCPP constructs) ← Older edit		Revision as of 06:33, 7 October 2010 (view source) NinaSchiller (Talk | contribs) (→Digestion) Newer edit →
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	Stored in -20 °C for later ligation.		Stored in -20 °C for later ligation.
		+
		+	----
		+	==Nina==
		+
		+	===Miniprep===
		+
		+	I performed a miniprep on IgG protease_Tra10_Ntermin#4 and Fusion_NS#2 according to the procedure that is described in protocols.
		+
		+	===Send for sequencing===
		+
		+	I sent two samples for seqeuncing. The mixture was 15 ul sample and 1.5 ul forward bank vector verification primer VF.
		+
		+	*IgG protease_Tra10_Ntermin#4 ASB0045 682
		+
		+	*Fusion_NS#2 ASB0045 681
		+
		+	===Overnight culture===
		+
		+	I inoculated 12 ml LB and 24 ul chloramphenicol with IgG protease_Tra10_Ntermin#6 again since I acidentally droped the previous sample and therefore lost it.
		+
		+	===iGEM Uppsala collaboration==
		+
		+	I drove to Uppsala and started a collaboration with their team. I obtained a construct that they want me/our group to PCR with verification primers (VF2 & VR) and run on an agarose gel. I in turn gave them the tyrosinase gene to also amplify via PCR but with own designed primers.
		+
		+	*Uppsala iGEM team's PCR master mix and prgm:
		+
		+	[[Image:Pq.jpg]]

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Revision as of 06:33, 7 October 2010

Contents 1 Andreas 1.1 LB agar plates 1.2 Assembly of His⋅SOD⋅cCPP constructs 1.2.1 Digestion 2 Nina 2.1 Miniprep 2.2 Send for sequencing 2.3 Overnight culture 3 =iGEM Uppsala collaboration

Andreas

LB agar plates

• 20 x 100 μg/ml Amp LB agar plates

Assembly of His⋅SOD⋅cCPP constructs

Digested pMA.His⋅SOD constructs for later assembly into cCPP plasmids, digested by Johan.

Digestion

	pMA.His⋅ SOD
10X FastDigest buffer	3
DNA (3 μg)	7.5
dH2O	17.5
FD EcoRI	1
FD AgeI	1
	30 μl

• Incubation: 37 °C, 0:30
• Inactivation: 80 °C, 20 min

Stored in -20 °C for later ligation.

---

Nina

Miniprep

I performed a miniprep on IgG protease_Tra10_Ntermin#4 and Fusion_NS#2 according to the procedure that is described in protocols.

Send for sequencing

I sent two samples for seqeuncing. The mixture was 15 ul sample and 1.5 ul forward bank vector verification primer VF.

• IgG protease_Tra10_Ntermin#4 ASB0045 682

• Fusion_NS#2 ASB0045 681

Overnight culture

I inoculated 12 ml LB and 24 ul chloramphenicol with IgG protease_Tra10_Ntermin#6 again since I acidentally droped the previous sample and therefore lost it.

=iGEM Uppsala collaboration

I drove to Uppsala and started a collaboration with their team. I obtained a construct that they want me/our group to PCR with verification primers (VF2 & VR) and run on an agarose gel. I in turn gave them the tyrosinase gene to also amplify via PCR but with own designed primers.

• Uppsala iGEM team's PCR master mix and prgm: