Difference between revisions of "Part:BBa K1675004"
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K1675004 short</partinfo> | <partinfo>BBa_K1675004 short</partinfo> | ||
− | The constitutive promoter J23119, the ribosome binding site B0034 and the functional gene NhaA were used in this new standard part. This part is available for the bacteria to survive in alkaline environment. | + | The strong constitutive promoter J23119, the ribosome binding site B0034 and the functional gene ''NhaA''([BBa_K1675000]) were used in this new standard part. This standard part is available for the bacteria to survive in alkaline environment. |
+ | |||
+ | We designed suitable primers and linked JBA (J23119+B0034+''NhaA'') with pSB1C3. The agarose gel electrophoresis analysis below (Fig.1) shows the positive clones of JBA. | ||
+ | |||
+ | [[File:Fig.5-a.png]] | ||
+ | |||
+ | Fig.1 The positive clones of JBA | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 00:30, 19 September 2015
J23119+B0034+NhaA(BBa_K1675000)
The strong constitutive promoter J23119, the ribosome binding site B0034 and the functional gene NhaA([BBa_K1675000]) were used in this new standard part. This standard part is available for the bacteria to survive in alkaline environment.
We designed suitable primers and linked JBA (J23119+B0034+NhaA) with pSB1C3. The agarose gel electrophoresis analysis below (Fig.1) shows the positive clones of JBA.
Fig.1 The positive clones of JBA
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 324 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 521
Illegal BamHI site found at 1058 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 384
- 1000COMPATIBLE WITH RFC[1000]