Template:Team:KULeuven/3 September 2009/VanillinProduction

From 2009.igem.org

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* PCR
* PCR
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** The PCR from yesterday went very well, we had a huge amount of amplified biobrick DNA of the different parts.
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** The PCR from yesterday went very well, we had a huge amount of amplified biobrick DNA of the different parts. Agarose gel electrophoresis was used to test if the different pieces of DNA created by PCR had the correct length.
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Agarose gel electrophoresis was used to test if the different pieces of DNA created by PCR had the correct length.
+
{| border ="1" align="center"
{| border ="1" align="center"
!| gene || concentration || 260/280 || 260/230
!| gene || concentration || 260/280 || 260/230
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** After the restriction, Sam5, Sam8 and terminator were ligated in a three-way ligation. The same was done for ech, fcs and terminator.
+
** After the restriction, Sam5, Sam8 and terminator were ligated in a three-way ligation. The same was done for ech, fcs and terminator. We also started a ligation of just Sam5 and Sam8 and ech and fcs.
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We also started a ligation of just Sam5 and Sam8 and ech and fcs.
+

Revision as of 07:15, 4 September 2009

  • PCR
    • The PCR from yesterday went very well, we had a huge amount of amplified biobrick DNA of the different parts. Agarose gel electrophoresis was used to test if the different pieces of DNA created by PCR had the correct length.
gene concentration 260/280 260/230
Sam5 361,6 1,91 2,13
Sam8 323,8 1,92 2,06
ech 236,5 1,91 2,24
fcs 321,4 1,90 2,22
    • Amplified DNA was purified and cut with different restriction enzymes. After restriction, DNA was purified again before ligation.
gene concentration 260/280 260/230
Sam5 21,8 1,65 1,33
Sam8 17,1 1,56 1,16
ech 13,8 1,78 1,46
fcs 20,9 1,70 0,20
    • After the restriction, Sam5, Sam8 and terminator were ligated in a three-way ligation. The same was done for ech, fcs and terminator. We also started a ligation of just Sam5 and Sam8 and ech and fcs.