Team:TU Darmstadt/protocols/InFusion

From 2013.igem.org

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4.  VolumeSet up the In-Fusion cloning reaction
4.  VolumeSet up the In-Fusion cloning reaction
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     reaction mixture (20 µL total volume)<br>
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     reaction mixture (20 µL total volume)<br><br>
         1µl pBAD1 (130 bp, c = 45 ng/µL, 45 ng)<br>
         1µl pBAD1 (130 bp, c = 45 ng/µL, 45 ng)<br>
         1µl pBAD4 (130 bp, c = 57,7 ng/µL, 58 ng)<br>
         1µl pBAD4 (130 bp, c = 57,7 ng/µL, 58 ng)<br>
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         3,5µl pSB1C3 (2100 bp, c = 120,8 ng/µL, 360 ng)<br>
         3,5µl pSB1C3 (2100 bp, c = 120,8 ng/µL, 360 ng)<br>
         4µl 5x InFusion Pfu MasterMix<br>
         4µl 5x InFusion Pfu MasterMix<br>
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         1,5µl nucleasefree H2O<br>
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         1,5µl nucleasefree H2O<br></font></p>
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5.  Incubate cloning reaction for 15 min at 50°C<br>
5.  Incubate cloning reaction for 15 min at 50°C<br>
6.  Transform competent E. coli with the reaction mixture<br>
6.  Transform competent E. coli with the reaction mixture<br>
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Revision as of 00:13, 5 October 2013





In Fusion

Materials

Equipment
In-Fusion® HD Cloning Kit
Micropipettes with sterile tips

Chemicals & consumables
5X In-Fusion HD Enzyme Premix
pUC19 Control Vector,linearized (50 ng/μl)
2 kb Control Insert (40 ng/μl)



Procedure
1. Generating linearized vector
2. Design gene-specific primers with 15 bp extensions homologous to vector end
3. Amplify your gene of interest
4. VolumeSet up the In-Fusion cloning reaction

reaction mixture (20 µL total volume)

1µl pBAD1 (130 bp, c = 45 ng/µL, 45 ng)
1µl pBAD4 (130 bp, c = 57,7 ng/µL, 58 ng)
1µl terminator (100 bp, c = 44 ng/µL, 44 ng)
3,5µl TLO (2440 bp, c = 241,7 ng/µL, 780 ng)
4,5µl CMK (1850 bp, c = 154,2 ng/µL, 680 ng)
3,5µl pSB1C3 (2100 bp, c = 120,8 ng/µL, 360 ng)
4µl 5x InFusion Pfu MasterMix
1,5µl nucleasefree H2O


5. Incubate cloning reaction for 15 min at 50°C
6. Transform competent E. coli with the reaction mixture