Team:TU Delft/21 June 2010 content

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===Lab work===
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==Lab work==
<h4>Characterization of Anderson RBS sequences</h4>  
<h4>Characterization of Anderson RBS sequences</h4>  
[[Team:TU_Delft/protocols/restriction_enzyme_digestion|Restriction digestion]] of plasmid backbone pSB1T3 using Buffer H of Roche.
[[Team:TU_Delft/protocols/restriction_enzyme_digestion|Restriction digestion]] of plasmid backbone pSB1T3 using Buffer H of Roche.
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Digestion reaction:needed fragment
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{| style="color:black; background-color:white;" cellpadding="5" cellspacing="0" border="1"
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|'''Digestion reaction'''
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* 1,0 μg pSB1T3 + 1 U/μL EcoRI and 1 U/μL PstI: ‘E – ---- – P’
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|'''Needed fragment'''
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|-
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|1,0 μg pSB1T3 + 1 U/μL EcoRI + 1 U/μL PstI
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|‘E – ---- – P’
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|}
The digested pSB1T3 was cut from gel and isolate the band.  
The digested pSB1T3 was cut from gel and isolate the band.  
However, the gel extraction kit didn’t work as well as we had hoped, it turned out to be the DNA disappearing kit. Tomorrow a new day.
However, the gel extraction kit didn’t work as well as we had hoped, it turned out to be the DNA disappearing kit. Tomorrow a new day.

Revision as of 17:45, 17 July 2010

Lab work

Characterization of Anderson RBS sequences

Restriction digestion of plasmid backbone pSB1T3 using Buffer H of Roche.

Digestion reaction Needed fragment
1,0 μg pSB1T3 + 1 U/μL EcoRI + 1 U/μL PstI ‘E – ---- – P’

The digested pSB1T3 was cut from gel and isolate the band. However, the gel extraction kit didn’t work as well as we had hoped, it turned out to be the DNA disappearing kit. Tomorrow a new day.