Difference between revisions of "Part:BBa K553002:Design"

 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K553002 short</partinfo>
 
<partinfo>BBa_K553002 short</partinfo>
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===Design Notes===
 
===Design Notes===
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the pcr amplification worked well, few mutation observed after sequencing that are present in our strain
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the pcr amplification worked well, few mutation observed after sequencing that are present in our strain  
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'''PromTraFw'''
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5' GTTTCTCGAATTCGCGGCCGCTTCTAGAGAAGTGCAGATTTGCACATGAAATCAACG 3'
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'''PromTra rev""
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5' GTTTCTTCCTGCAGCGGCCGCTACTAGTATAGCGGAGAGAAAACATCTCATTCAGG 3'
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pcr protocol:
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95° 5' | 10x (93° 30" | 56° 30" | 72° 40") | 23x ( (93° 30" | 65° 30" | 72° 40") | 72° 7' | 4° ∞
  
  
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----
  
 
===Source===
 
===Source===

Latest revision as of 13:44, 19 September 2011

PTraI - TraR-OC8 HLA complex regulated promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 105
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

the pcr amplification worked well, few mutation observed after sequencing that are present in our strain

PromTraFw

5' GTTTCTCGAATTCGCGGCCGCTTCTAGAGAAGTGCAGATTTGCACATGAAATCAACG 3'

PromTra rev""

5' GTTTCTTCCTGCAGCGGCCGCTACTAGTATAGCGGAGAGAAAACATCTCATTCAGG 3'

pcr protocol:

95° 5' | 10x (93° 30" | 56° 30" | 72° 40") | 23x ( (93° 30" | 65° 30" | 72° 40") | 72° 7' | 4° ∞


Source

http://www.ncbi.nlm.nih.gov/nucleotide/8572673?report=genbank&log$=nuclalign&blast_rank=1&RID=795BNUZN014

References