2006
DOI: 10.1016/j.ymthe.2006.08.397
|View full text |Cite
|
Sign up to set email alerts
|

340. Cellular Uptake and Subsequent Intracellular of R8-Liposomes Introduced at Low Temperature

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2012
2012
2012
2012

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…92 Figure 14.9 shows an example of intracellular traffi cking of lipoplexes being visualized using LCSM; the plasma membrane of target cell was stained with PKH67 (green fl uorescent dye), and the lipoplexes were labeled with red fl uorescent dye, so the cellular uptake and nuclear entry of lipoplex can be observed. 93 For DNA delivery, it is useful to employ a plasmid that encodes reporter genes, such as green fl uorescence protein ( GFP ) or luciferase, which allows the transfection effi ciency to be measured using simple assays. For siRNA delivery, it may be useful to employ cell lines that stably express reporter gene GFP and luciferase, so that the transfection effi ciency and the degree of gene knockdown can be measured easily.…”
Section: Flow Cytometry and Confocal Microscopy Studiesmentioning
confidence: 99%
“…92 Figure 14.9 shows an example of intracellular traffi cking of lipoplexes being visualized using LCSM; the plasma membrane of target cell was stained with PKH67 (green fl uorescent dye), and the lipoplexes were labeled with red fl uorescent dye, so the cellular uptake and nuclear entry of lipoplex can be observed. 93 For DNA delivery, it is useful to employ a plasmid that encodes reporter genes, such as green fl uorescence protein ( GFP ) or luciferase, which allows the transfection effi ciency to be measured using simple assays. For siRNA delivery, it may be useful to employ cell lines that stably express reporter gene GFP and luciferase, so that the transfection effi ciency and the degree of gene knockdown can be measured easily.…”
Section: Flow Cytometry and Confocal Microscopy Studiesmentioning
confidence: 99%