Reporter

Part:BBa_K1041002:Experience

Designed by: NRP UEA   Group: iGEM13_NRP-UEA-Norwich   (2013-08-15)
Revision as of 11:19, 17 September 2013 by Holusac (Talk | contribs) (Team NRP-UEA_Norwich 2013)


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Team NRP-UEA_Norwich 2013

Team NRP-UEA_Norwich 2013 created this part using biobricks BBa_K1041000 and BBa_K1041001. These biobricks both contain a Nde1 site after their promoter sequence, enabling a restriction digest to be performed. The RFP coding gene was excised from BBa_K1041000 and ligated in front of the AntG promoter of BBa_K1041001 to create a new biobrick.

Characterisation of this biobrick involved comparisons with the original Bba_J04450 biobrick by performing transformations, restriction digests and BLAST analysis. We also had our biobrick sequenced.

Sequencing

The biobrick was sent off to a company for sequencing.

K1041000 sequencing data part 1
K1041000 sequencing data part 2
K1041000 sequencing data part 3










BLAST Analysis

The data we recieved back from the sequencing company was aligned using BLAST with the expected DNA sequence fig.2

User Reviews

UNIQ186eb371801a01ce-partinfo-00000000-QINU UNIQ186eb371801a01ce-partinfo-00000001-QINU

User Reviews

UNIQ186eb371801a01ce-partinfo-00000002-QINU UNIQ186eb371801a01ce-partinfo-00000003-QINU