Difference between revisions of "Part:BBa K1041002"

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===BLAST Analysis===
 
===BLAST Analysis===
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The data we recieved back from the sequencing company was aligned using BLAST with the expected DNA sequence ''Fig 5,6''
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The data we recieved back from the sequencing company was aligned using BLAST with the expected DNA sequence ''Fig 5,6''The sequencing with both the forward and reverse primers had over 96& matches.
 
[[image:6 Fwd.JPG|thumb|left|Fig 5: Forward primer K1041002 sequencing data aligned with the expected DNA sequence]]
 
[[image:6 Fwd.JPG|thumb|left|Fig 5: Forward primer K1041002 sequencing data aligned with the expected DNA sequence]]
 
[[image:6 Rev.JPG|thumb|left|Fig 6: Reverse primer K1041002 sequencing data aligned with the expected DNA sequence]]
 
[[image:6 Rev.JPG|thumb|left|Fig 6: Reverse primer K1041002 sequencing data aligned with the expected DNA sequence]]

Revision as of 10:59, 23 September 2013

AntG Promoter + RFP Coding Device

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.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 683
    Illegal AgeI site found at 795
  • 1000
    COMPATIBLE WITH RFC[1000]


Characterisation

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 recieved showed the DNA is good quality Fig 2,3,4..

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