Difference between revisions of "Part:BBa K1456004:Experience"
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==Luciferase Assay== | ==Luciferase Assay== | ||
<li>The vectors isolated from the colonies we identified correct are co-transfected into HEK293 and HepG2 cell lines. Transfected cells are incubated in hypoxic and normoxic conditions and the luminescence levels are measured by performing luciferase assay. To conduct hypoxic condition, we used 100 uM CoCl2. Here, the graphics we obtained after the measurement of luminescence is shown below. | <li>The vectors isolated from the colonies we identified correct are co-transfected into HEK293 and HepG2 cell lines. Transfected cells are incubated in hypoxic and normoxic conditions and the luminescence levels are measured by performing luciferase assay. To conduct hypoxic condition, we used 100 uM CoCl2. Here, the graphics we obtained after the measurement of luminescence is shown below. | ||
− | <center>[[File:Atoms hre 4.png| | + | <center>[[File:Atoms hre 4.png|700px|]]</center> <br/> |
<li>According to the results, in hypoxic conditions comparing with normoxia, HRE been inserted into pTRE-luciferase vector shows 7 times more activity by producing more luciferase in HepG2 cell line. In HEK293 cell line, this activity is measured in hypoxia 1,5 times more than normoxia. This results prove that HRE sequence improves the production rate of desired protein in hypoxia comparing with normal oxygen levels. | <li>According to the results, in hypoxic conditions comparing with normoxia, HRE been inserted into pTRE-luciferase vector shows 7 times more activity by producing more luciferase in HepG2 cell line. In HEK293 cell line, this activity is measured in hypoxia 1,5 times more than normoxia. This results prove that HRE sequence improves the production rate of desired protein in hypoxia comparing with normal oxygen levels. | ||
− | <center>[[File:Atoms hre 5.png| | + | <center>[[File:Atoms hre 5.png|700px|]]</center> <br/> |
+ | ==CopGFP Assay== | ||
+ | <li>The vectors isolated from the colonies we identified correct are co-transfected into HEK293 and HepG2 cell lines. Transfected cells are incubated in hypoxic and normoxic conditions and the luminescence levels are measured by performing luciferase assay. To conduct hypoxic condition, we used 100 uM CoCl2. Here, the graphics we obtained after the measurement of luminescence is shown below. | ||
+ | <center>[[File:Atoms hre 4.png|700px|]]</center> <br/> | ||
+ | <li>According to the results, in hypoxic conditions comparing with normoxia, HRE been inserted into pTRE-luciferase vector shows 7 times more activity by producing more luciferase in HepG2 cell line. In HEK293 cell line, this activity is measured in hypoxia 1,5 times more than normoxia. This results prove that HRE sequence improves the production rate of desired protein in hypoxia comparing with normal oxygen levels. | ||
+ | <center>[[File:Atoms hre 5.png|700px|]]</center> <br/> | ||
Latest revision as of 04:23, 10 October 2018
Luciferase Assay
CopGFP Assay
Applications of BBa_K1456004
User Reviews
UNIQeef3718e07a63f5d-partinfo-00000000-QINU
UNIQeef3718e07a63f5d-partinfo-00000001-QINU