Difference between revisions of "Part:BBa K215002"

 
Line 1: Line 1:
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K215002 short</partinfo>
 
<partinfo>BBa_K215002 short</partinfo>
  
nnn
+
For example, assume our gene (E0040) starts with:
 +
5'-atgcgtaaaggagaagaacttt...-3'
 +
 
 +
The design process would be:
 +
# Start with the XbaI site: 5'-TCTAGA-3'
 +
# Add ~20bp of the gene immediately after the XbaI site, starting _after_ the start codon (atg), and try to end on a G or C: 5'-TCTAGAcgtaaaggagaagaacttt-3' for E0040 from above.  These ~20bp will determine the melting temperature for the primer.
 +
# Add 6-8 random nucleotides at the start.  Try to balance out the primer to ~%50 g&c to a&t: 5'-cgggcTCTAGAcgtaaaggagaagaacttt-3'
 +
# Tweak the number of nucleotides until the melting point roughly matches that of Vr.
 +
 
 +
Then to add the gene to the construct, again assuming the gene is a biobrick with standard suffix:
 +
# PCR with the designed forward primer and Vr
 +
# Then run the PCR product in a digest with XbaI and PstI, and digest this part (the display construct) with NheI and PstI.  The XbaI site has a sticky end that binds with NheI.
 +
# Standard ligation and transformation.
 +
 
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 05:17, 1 October 2009

pLac+RBS+Secretion Signal and Streptavidin Binding Tags

For example, assume our gene (E0040) starts with: 5'-atgcgtaaaggagaagaacttt...-3'

The design process would be:

  1. Start with the XbaI site: 5'-TCTAGA-3'
  2. Add ~20bp of the gene immediately after the XbaI site, starting _after_ the start codon (atg), and try to end on a G or C: 5'-TCTAGAcgtaaaggagaagaacttt-3' for E0040 from above. These ~20bp will determine the melting temperature for the primer.
  3. Add 6-8 random nucleotides at the start. Try to balance out the primer to ~%50 g&c to a&t: 5'-cgggcTCTAGAcgtaaaggagaagaacttt-3'
  4. Tweak the number of nucleotides until the melting point roughly matches that of Vr.

Then to add the gene to the construct, again assuming the gene is a biobrick with standard suffix:

  1. PCR with the designed forward primer and Vr
  2. Then run the PCR product in a digest with XbaI and PstI, and digest this part (the display construct) with NheI and PstI. The XbaI site has a sticky end that binds with NheI.
  3. Standard ligation and transformation.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 196
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]