Difference between revisions of "Part:BBa K896002:Design"

 
(Design Notes)
Line 1: Line 1:
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K896002 short</partinfo>
 
<partinfo>BBa_K896002 short</partinfo>
Line 7: Line 6:
  
 
===Design Notes===
 
===Design Notes===
YES
 
  
 +
1. Endogenious EcoRI site is at 655bp, and PstI is at 121bp.
 +
 +
2. Instead of mutant ctting site, we created a smart pSB1C3 plasmid (MfeI-XbaI -pSB1C3-SbfI-SpeI)for CysI cloning.
 +
 +
3. Taking advantage of MfeI and EcoRI are compatible; SbfI and XbaI are compatible.
 +
 +
4. Vector: MfeI-XbaI -pSB1C3-SbfI-SpeI, cut with MfeI and SbfI
  
 +
5. Insert: CysI, cut with EcoRI and XbaI
  
 
===Source===
 
===Source===

Revision as of 19:15, 26 September 2012

Dsr (sulfite reductase)


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 1636
    Illegal EcoRI site found at 4648
    Illegal PstI site found at 826
    Illegal PstI site found at 3838
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 1636
    Illegal EcoRI site found at 4648
    Illegal PstI site found at 826
    Illegal PstI site found at 3838
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 1636
    Illegal EcoRI site found at 4648
    Illegal BglII site found at 1091
    Illegal BglII site found at 4103
    Illegal BamHI site found at 3007
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 1636
    Illegal EcoRI site found at 4648
    Illegal PstI site found at 826
    Illegal PstI site found at 3838
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 1636
    Illegal EcoRI site found at 4648
    Illegal PstI site found at 826
    Illegal PstI site found at 3838
    Illegal NgoMIV site found at 1741
    Illegal NgoMIV site found at 4753
    Illegal AgeI site found at 406
    Illegal AgeI site found at 1261
    Illegal AgeI site found at 3418
    Illegal AgeI site found at 4273
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

1. Endogenious EcoRI site is at 655bp, and PstI is at 121bp.

2. Instead of mutant ctting site, we created a smart pSB1C3 plasmid (MfeI-XbaI -pSB1C3-SbfI-SpeI)for CysI cloning.

3. Taking advantage of MfeI and EcoRI are compatible; SbfI and XbaI are compatible.

4. Vector: MfeI-XbaI -pSB1C3-SbfI-SpeI, cut with MfeI and SbfI

5. Insert: CysI, cut with EcoRI and XbaI

Source

YES

References