Difference between revisions of "Part:BBa K3171177"

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<partinfo>BBa_K3171177 short</partinfo>
 
<partinfo>BBa_K3171177 short</partinfo>
  
We experimented with CRISPR with the aim to make a histidine auxotroph by knocking out HisD in both E. coli and V. natriegens. To make a histidine auxotroph by knocking out HisD in E. coli specific gRNA targets were selected for knockout of the HisD gene. We designed 3 homologous parts [[Part:BBa_K3171177]], [[Part:BBa_K3171178]], [[Part:BBa_K3171179]] in order to decide on the correct homologous part. 3 gRNA target sites (BBa_K3171180, BBa_K3171181, BBa_K3171182) were selected for knock out which.
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We experimented with CRISPR with the aim to make a histidine auxotroph by knocking out HisD in both E. coli and V. natriegens. To make a histidine auxotroph by knocking out HisD in E. coli specific gRNA targets were selected for knockout of the HisD gene. We designed 3 homologous parts [[Part:BBa_K3171177]], [[Part:BBa_K3171178]], [[Part:BBa_K3171179]] in order to decide on the correct homologous part required for knockout. 3 gRNA target sites [[Part:BBa_K3171180]], [[Part:BBa_K3171181]], [[Part:BBa_K3171182]] were selected for knock out.
  
 
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Revision as of 17:55, 20 October 2019


HisD 3000bp Homologous part 1

We experimented with CRISPR with the aim to make a histidine auxotroph by knocking out HisD in both E. coli and V. natriegens. To make a histidine auxotroph by knocking out HisD in E. coli specific gRNA targets were selected for knockout of the HisD gene. We designed 3 homologous parts Part:BBa_K3171177, Part:BBa_K3171178, Part:BBa_K3171179 in order to decide on the correct homologous part required for knockout. 3 gRNA target sites Part:BBa_K3171180, Part:BBa_K3171181, Part:BBa_K3171182 were selected for knock out.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 689
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1472
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 689
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 689
    Illegal AgeI site found at 1885
    Illegal AgeI site found at 2788
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 807