2013
DOI: 10.1007/978-1-62703-718-1_15
|View full text |Cite
|
Sign up to set email alerts
|

Cell-Based Bioluminescence Screening Assays

Abstract: Drug screening is an essential and widely used technique for drug discovery in various biomedical fields notably in oncology. Here we describe a functional screening assay based on the bioluminescence detection of a secreted luciferase for monitoring cell viability of cancer cells in a high-throughput format. This assay allows the screening of large libraries comprising thousands of compounds and the identification of potential anticancer molecules in a rapid, facile, and cost-effective manner.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2019
2019
2019
2019

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 16 publications
0
1
0
Order By: Relevance
“…To monitor activation of transcription factors/pathways such as Nuclear factor kappa-light-chain-enhancer of activated B cells (NFkB), the reporter of choice is cloned under the control of NFkB responsive elements [57]. The most effective way to engineer GSCs to express these reporters is to use lentivirus vectors, as adding the vector directly to the conditioned medium of GSCs results in >90% transduction efficiency and allows for integration of the expression cassette into the genome of cells, yielding stable expression of the reporter [59,60,61].…”
Section: In Vivo Gbm Modelmentioning
confidence: 99%
“…To monitor activation of transcription factors/pathways such as Nuclear factor kappa-light-chain-enhancer of activated B cells (NFkB), the reporter of choice is cloned under the control of NFkB responsive elements [57]. The most effective way to engineer GSCs to express these reporters is to use lentivirus vectors, as adding the vector directly to the conditioned medium of GSCs results in >90% transduction efficiency and allows for integration of the expression cassette into the genome of cells, yielding stable expression of the reporter [59,60,61].…”
Section: In Vivo Gbm Modelmentioning
confidence: 99%