Construction of different mutants of HA-tagged human RAGE gene and their eukaryotic expression / 南方医科大学学报
Journal of Southern Medical University
; (12): 1779-1781, 2008.
Article
in Zh
| WPRIM
| ID: wpr-340729
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To construct eukaryotic expression vectors for HA-tagged receptor for advanced glycation end products (RAGE) mutants.</p><p><b>METHODS</b>Site-directed mutagenesis was applied to wild-type RAGE gene cloned in the pcDNA3 vector with HA tag to obtain the mutants pcDNA3-HA-RAGE(S391A), pcDNA3-HA-RAGE(S399A), pcDNA3-HA-RAGE(S400A), and pcDNA3-HA-RAGE(T401A). After identification by sequencing, the mutants were transfected into HEK293 cells, and the expression of these mutants were detected by Western blotting using anti-HA antibody.</p><p><b>RESULTS</b>The HA-tagged RAGE mutants constructed were verified successfully by sequencing, and highly expressed in HEK293 cells.</p><p><b>CONCLUSION</b>The success in constructing HA-tagged RAGE mutants, which are highly expressed in eukaryotic cells, may facilitate the functional study of RAGE in cell signal transduction.</p>
Full text:
1
Index:
WPRIM
Main subject:
Receptors, Immunologic
/
Cell Line
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Mutagenesis, Site-Directed
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Cloning, Molecular
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Eukaryotic Cells
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Receptor for Advanced Glycation End Products
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Genetic Vectors
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Genetics
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Metabolism
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Mutation
Limits:
Humans
Language:
Zh
Journal:
Journal of Southern Medical University
Year:
2008
Type:
Article