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Yeast SUSY7/ ura3 strain cells transformed with TaSUT2A, TaSUT2B and TaSUT2D were able to uptake sucrose and grow on a medium containing sucrose as a sole source of carbon; however, our subcellular localization study with plant cells revealed that TaSUT2 is localized to the tonoplast.
The localization study indicated the distribution of ASNase2 in vascular tissues.
Localization study revealed that Cg-Mpeg1 protein is found primarily in late endosomes.
Further, the in vitro fluorescence imaging as well as localization study of QDs were performed in various cells.
We investigated whether ultrasonography performed by the operating surgeon (SUS) could be the initial and only preoperative localization study in patients with sporadic primary hyperparathyroidism.
Our localization study in this work expands previous works, since the localization of ASNase was only investigated in Scots pine (Canas et al. 2007) or Arabidopsis (Ivanov et al. 2012), but not in rice.
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Subcellular localization studies showed that all the OsGLRs examined are likely localized to the plasma membrane.
Subcellular localization studies showed that PMoV MP locates at PD.
Hence, TMAOH-SPMNP and COO-TMACl-SPMNP were not used further in this subcellular localization studies.
Complexes made with lactosylated PEI were then labeled and their localization studied by confocal microscopy.
This makes these systems very interesting for light localization studies, as proposed by Kohmoto et al. [15].
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