1
Optimal expression in HEK293 cells was determined by a time course analysis.
2
Ion channels were expressed in HEK293 cells and studied using patch-clamp recordings.
3
The reproducibility of these methods was further verified in the HEK293FT cell line.
4
HEK293 cell transplantation caused no difference compared to SCI + PBS group.
5
Two different types BK channels were constructed in HEK293 cells to investigate the regulation mechanism.
6
The endogenous TSP-1 mRNA half-life is approximately 2.0 hours in HEK293 cells.
7
Whole-cell patch-clamp measurements were made at 37 °C from hERG-expressing HEK293 cells.
8
In this chapter we describe methods for the heterologous expression of plant GTs using the HEK293 expression platform.
9
The stable HEK293 cell line of Pink1 expression was established through the lentivirus system.
10
The H87C mutant also failed to transfer its iron to mitochondria in HEK293 cells.
11
We cloned CgMTF-1 and determined the subcellular locations of its protein product in HEK293 cells.
12
Increased messenger RNA stability was detected in HEK293 cells, indicating that this was the cause of the higher protein levels.
13
Graham planned to use HEK293 cells to study mechanisms underlying cancer, and distributed them to researchers all over the world.
14
Therefore SOCE was examined in HEK293 cells microscopically with the fura-2 technique and with patch clamp.
15
Reporter activity was abrogated in isolated mutant proximal or distal miR-506 constructs in miR-506-transfected HEK293 cells.
16
When the gene was transfected into HEK293 cells in a GFP fusion vector, the protein was specifically localized in the cytosol.