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Team:TU Darmstadt/protocols/InFusion
From 2013.igem.org
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<img alt="team" src="/wiki/images/4/4c/10._Labbook_(angewählt).jpg" width="90" height="30"></a> | <img alt="team" src="/wiki/images/4/4c/10._Labbook_(angewählt).jpg" width="90" height="30"></a> | ||
| - | </div> | + | </div><br> |
| + | <br><br><br><br> | ||
| + | <center> | ||
| + | <a href="https://2013.igem.org/Team:TU_Darmstadt/labbook"> | ||
| + | <font size="8" color="#F0F8FF" face="Arial regular">Lab book |</font> | ||
| + | </a> | ||
| + | <a href="https://2013.igem.org/Team:TU_Darmstadt/materials"> | ||
| + | <font size="8" color="#F0F8FF" face="Arial regular">Materials |</font> | ||
| + | </a> | ||
| + | <a href="https://2013.igem.org/Team:TU_Darmstadt/protocols"> | ||
| + | <font size="8" color="#F0F8FF" face="Arial regular">Protocols</font> | ||
| + | </a> | ||
| + | </center> | ||
| + | <br> | ||
<!-- In Fusion --> | <!-- In Fusion --> | ||
<center> | <center> | ||
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<h2><font size="6" color="#F0F8FF" face="Arial regular"> In Fusion </font></h2> | <h2><font size="6" color="#F0F8FF" face="Arial regular"> In Fusion </font></h2> | ||
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4. VolumeSet up the In-Fusion cloning reaction | 4. VolumeSet up the In-Fusion cloning reaction | ||
<p text-aligne:left style="margin-left:60px; margin-right:50px"><font size="3" color="#F0F8FF" face="Arial regular"> | <p text-aligne:left style="margin-left:60px; margin-right:50px"><font size="3" color="#F0F8FF" face="Arial regular"> | ||
| - | reaction mixture (20 µL total volume)<br> | + | 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> | ||
| - | 1,5µl nucleasefree H2O<br> | + | 1,5µl nucleasefree H2O<br></font></p> |
| - | <br> | + | |
| - | < | + | <br><font size="3" color="#F0F8FF" face="Arial regular"> |
| + | <p text-aligne:left style="margin-left:50px; margin-right:50px"> | ||
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> | ||
<br> | <br> | ||
Latest revision as of 00:36, 5 October 2013
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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
