Difference between revisions of "Part:BBa K1041002:Experience"

Revision as of 10:59, 23 September 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 sequencing, restriction digests and BLAST analysis.

Restriction Digest

Part Bba_K1041002 was digested with enzymes XbaI and NdeI and compared to uncut DNA Fig 1.

Fig 1:Lane 1 contains and Bba_K1041002 cut with XbaI and NdeI and lane 2 uncut Bba_K1041002.

Sequencing

The biobrick was sent off to a company for sequencing and the data we received back Fig 2,3,4 showed the DNA is good quality.

Fig 2:K1041002 sequencing data part 1

Fig 3:K1041002 sequencing data part 2

Fig 4:K1041002 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 5,6The sequencing with both the forward and reverse primers had over 96% matches.

Fig 5: Forward primer K1041002 sequencing data aligned with the expected DNA sequence

Fig 6: Reverse primer K1041002 sequencing data aligned with the expected DNA sequence

User Reviews

UNIQea8108d76e812131-partinfo-00000000-QINU UNIQea8108d76e812131-partinfo-00000001-QINU