Team:Kyoto/GoldenGateAssembly/Notebook

From 2012.igem.org

(Difference between revisions)
(Golden Gate Assembly Notebook)
(Golden Gate Assembly Notebook)
Line 9: Line 9:
==September 6==
==September 6==
-
====PCR====
+
====PCR and Electrophoresis assay====
①psB1K3
①psB1K3
②lacI
②lacI
Line 26: Line 26:
==September 7==
==September 7==
-
====Electrophoresis assay====
+
 
-
①psB1K3
+
====PCR and Electrophoresis assay====
-
②lacI
+
-
③GFP
+
-
④GFP
+
-
⑤RFP
+
-
⑥RFP
+
-
⑦CFP
+
-
⑧DT
+
-
====PCR of psB1K3====
+
{|class="wikitable"
{|class="wikitable"
-
!10x Buffer!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(psB1K3)!!KOD plus!!milliQ!!total
+
!10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(psB1K3)!!KOD plus!!milliQ!!total
|-
|-
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25
|}
|}
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min
 +
 +
==September 10==
 +
====PCR and Electrophoresis assay====
 +
{|class="wikitable"
 +
!10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(CFP)!!KOD plus!!milliQ!!total
 +
|-
 +
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25
 +
|}
 +
94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 45sec
 +
 +
====PCR and Electrophoresis assay====
 +
{|class="wikitable"
 +
!10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(lacI)!!KOD plus!!milliQ!!total
 +
|-
 +
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25
 +
|}
 +
94℃ 2min, (94℃ 15sec, 51℃ 30sec)x30cycles, 68℃ 30sec
 +
 +
====PCR and Electrophoresis assay====
 +
①PCR product of psB1K3
 +
②psB1K3
 +
③psB1C3
 +
④psB1K3
 +
⑤PCR product of CFP
 +
{|class="wikitable"
 +
!10x Buffer KOD plus!!2mM dNTPs!!25mM MgSO4!!F primer!!R primer!!DNA(lacI)!!KOD plus!!milliQ!!total
 +
|-
 +
|2.5||2.5||1.0||0.75||0.75||0.5||0.5||16.5||25
 +
|}
 +
94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec
 +
</div>
</div>
{{Kyoto/footer}}
{{Kyoto/footer}}

Revision as of 08:16, 20 September 2012

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Contents

Golden Gate Assembly Notebook

August 10

Golden Gate Assembly method This method helps us to constract some genes quickly and we can design the order of constractions. We are trying to construct a gene cycle composed of 6 genes( pSB1A3, lacI, GFP, RFP, GFP, DT). After this experiment is confirmed to work, we will so some experiment to check how the numbers of promorters influences the strength of transcription.

September 6

PCR and Electrophoresis assay

①psB1K3 ②lacI ③GFP ④GFP ⑤RFP ⑥RFP ⑦CFP ⑧DT

Quick Taqprimer Fprimer RDNA(①-⑧)MilliQTotal
12.50.50.5110.525

94℃ 2min, (94℃ 30sec, 50℃ 30sec)x25cycles, 68℃ 50sec

September 7

PCR and Electrophoresis assay

10x Buffer KOD plus2mM dNTPs25mM MgSO4F primerR primerDNA(psB1K3)KOD plusmilliQtotal
2.52.51.00.750.750.50.516.525

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min

September 10

PCR and Electrophoresis assay

10x Buffer KOD plus2mM dNTPs25mM MgSO4F primerR primerDNA(CFP)KOD plusmilliQtotal
2.52.51.00.750.750.50.516.525

94℃ 2min, (94℃ 15sec, 48℃ 30sec)x30cycles, 68℃ 45sec

PCR and Electrophoresis assay

10x Buffer KOD plus2mM dNTPs25mM MgSO4F primerR primerDNA(lacI)KOD plusmilliQtotal
2.52.51.00.750.750.50.516.525

94℃ 2min, (94℃ 15sec, 51℃ 30sec)x30cycles, 68℃ 30sec

PCR and Electrophoresis assay

①PCR product of psB1K3 ②psB1K3 ③psB1C3 ④psB1K3 ⑤PCR product of CFP

10x Buffer KOD plus2mM dNTPs25mM MgSO4F primerR primerDNA(lacI)KOD plusmilliQtotal
2.52.51.00.750.750.50.516.525

94℃ 2min, (94℃ 15sec, 58℃ 30sec)x30cycles, 68℃ 2min20sec