Difference between revisions of "Part:BBa K1216004"
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
− | <partinfo> | + | <partinfo>BBa_K1216000 short</partinfo> |
− | gusA enzyme | + | ''gusA'' (also called uidA[[Part:BBa_K1216000#References|<sup>[1]</sup>]]) encodes β-Glucuronidase, an intracellular enzyme that catalyzes the hydrolysis of β-D-glucuronides. [[File:Glucuronidase_3d_model.jpg|thumb| 3D representation of the β-Glucuronidase from [http://www.rcsb.org/pdb/explore/explore.do?structureId=3K46 RCSB] ]] |
− | |||
− | |||
+ | A form of this protein with added TEV and poly-HIS tags can be found [[Part:BBa_K1216004| here]]. | ||
+ | |||
+ | ===Usage and Biology=== | ||
+ | β-Glucuronidase is used as a fusion protein marker in higher plants, due to them lacking intrinsic β-Glucuronidase activity[[Part:BBa_K1216000#References|<sup>[2]</sup>]]. | ||
+ | Generally it can be used as reporter enzyme with detection by biochemical activity assays, immunological assays or by histochemical staining of tissue sections or cells[[Part:BBa_K1216000#References|<sup>[3]</sup>]]. | ||
<!-- --> | <!-- --> | ||
+ | |||
+ | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
− | <partinfo> | + | <partinfo>BBa_K1216000 SequenceAndFeatures</partinfo> |
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
===Functional Parameters=== | ===Functional Parameters=== | ||
− | <partinfo> | + | <partinfo>BBa_K1216000 parameters</partinfo> |
<!-- --> | <!-- --> | ||
+ | |||
+ | |||
+ | ===References=== | ||
+ | # [http://ecoliwiki.net/colipedia/index.php/uidA:Gene ecoliwiki] | ||
+ | # Jefferson A R, "GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants.", EMBO J. 1987 December 20; 6(13): 3901–3907 [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC553867/] | ||
+ | # [http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/gusabul.Par.0001.File.tmp/gusabul.pdf Sigma Aldrich] |
Revision as of 13:01, 6 September 2013
β-Glucuronidase (gusA) from Bacillis Subtilis
gusA (also called uidA[1]) encodes β-Glucuronidase, an intracellular enzyme that catalyzes the hydrolysis of β-D-glucuronides.
A form of this protein with added TEV and poly-HIS tags can be found here.
Usage and Biology
β-Glucuronidase is used as a fusion protein marker in higher plants, due to them lacking intrinsic β-Glucuronidase activity[2]. Generally it can be used as reporter enzyme with detection by biochemical activity assays, immunological assays or by histochemical staining of tissue sections or cells[3].
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 538
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
- [http://ecoliwiki.net/colipedia/index.php/uidA:Gene ecoliwiki]
- Jefferson A R, "GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants.", EMBO J. 1987 December 20; 6(13): 3901–3907 [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC553867/]
- [http://www.sigmaaldrich.com/etc/medialib/docs/Sigma/Bulletin/gusabul.Par.0001.File.tmp/gusabul.pdf Sigma Aldrich]