Team:Paris/17 August 2009
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Cha.olivier (Talk | contribs) (→Lab work) |
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65°C for 20 min for heat inactivation | 65°C for 20 min for heat inactivation | ||
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+ | </div> | ||
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+ | <div class="charlotte"> | ||
+ | Transformation | ||
+ | </div> | ||
+ | <div class="experience"> | ||
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+ | Transformation of BBa_B0034 (AmpR), BBa_E0030(KanR), pSB3C5 (CmR), pINTE3 (AmpR), pTA (AmpR), pINTg3p (AmpR) and pINK2 using the "heat choc" protocol | ||
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+ | </div> | ||
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+ | <div class="charlotte"> | ||
+ | Ligation | ||
+ | </div> | ||
+ | <div class="experience"> | ||
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+ | Ligation of pSB1A3 and A11 or A13 | ||
</div> | </div> |
Revision as of 10:00, 17 August 2009
Contents |
NoteBook
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Brain work
edit please ^^
Lab work
Vector Dephosphorylation
Dephosphorylation:
pSB1A3 digested by EcoRI/PstI, XbaI/PstI and EcoRI/SpeI have to be dephosphorylated before the ligation process.
Mix : Vector : 30uL
Antarctic Phosphatase : 2uL
Buffer : 3,5 uL
Put the solution at 37°C for 30 min
Add 2 uL of enzyme
37°C for 30 min
65°C for 20 min for heat inactivation
Transformation
Transformation of BBa_B0034 (AmpR), BBa_E0030(KanR), pSB3C5 (CmR), pINTE3 (AmpR), pTA (AmpR), pINTg3p (AmpR) and pINK2 using the "heat choc" protocol
Ligation
Ligation of pSB1A3 and A11 or A13
To do list
edit please ^^