Difference between revisions of "Part:BBa K896999:Design"

 
(Design Notes)
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<partinfo>BBa_K896999 short</partinfo>
 
<partinfo>BBa_K896999 short</partinfo>
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===Design Notes===
 
===Design Notes===
Many design considerations were taken into account when creating this sequence
+
Primers used in the PCR:
 
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X174_E_FP: gcttctag atggtacgctggactttgt (TM:55C)
 
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X174_E_RP: gct ctgcagcggccgctactagta tcactccttccgcacg (TM:55C)
 +
Digested the PCR product with XbaI and PstI, and ligated the digestion product with a gel purified XbaI,PstI digested pSB1A2 plasmid backbone.
  
 
===Source===
 
===Source===

Revision as of 04:17, 5 April 2012

ΦX174; E (lysis) gene


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Primers used in the PCR:

X174_E_FP: gcttctag atggtacgctggactttgt (TM:55C)
X174_E_RP: gct ctgcagcggccgctactagta tcactccttccgcacg (TM:55C)

Digested the PCR product with XbaI and PstI, and ligated the digestion product with a gel purified XbaI,PstI digested pSB1A2 plasmid backbone.

Source

From where

References