8µL of 2.1 purify PCR products, 8µL of 2.2 purify PCR products, 2µL of ligase T4 Buffer and 2L of ligase T4 were mixed. 8µL of 3.1 purify PCR products, 8µL of 3.2 purify PCR products, 2µL of ligase T4 Buffer and 2µL of ligase T4 were mixed. They were incubated for 1h at RT.
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8µL of 2.1 purify PCR products, 8µL of 2.2 purify PCR products, 2µL of ligase T4 Buffer and 2L of ligase T4 were mixed. 8µL of 3.1 purified PCR products, 8µL of 3.2 purified PCR products, 2µL of ligase T4 Buffer and 2µL of ligase T4 were mixed. They were incubated for 1h at RT.
Line 67:
Line 67:
The specific [[Team:Paris_Saclay/Experiments#primers|primers]] for each parts were using.
The specific [[Team:Paris_Saclay/Experiments#primers|primers]] for each parts were using.
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The products were put to migrated on a 0.8%agarose gel with BET.
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The products were put to migrated on a 0.8% agarose gel with BET.
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==== PCR Clean-up with the NucleoSpin kit ====
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''By Mahnaz''
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The purification was carried out on PCR product PSB1C3 and 4.2 also the ligation products PS16003-PS16004 and PS16005-PS16006 following the usual [[Team:Paris_Saclay/Experiments#Purification|protocol]].
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==== 4.1-4.2 ligation ====
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''By Mahnaz''
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8µL of 4.1 purified PCR products, 8µL of 4.2 purified PCR products, 2µL of ligase T4 Buffer and 2L of ligase T4 were mixed. The ligation reaction mixture were incubated for overnight in the 4°c.