U87 MG In Vitro Caspase Activation-based Apoptosis Assay (FCM)
CAT#: ITS-1022-YF352
Target Cell Organism: Human
Target Cell Alternative Name: U87MG; U-87 MG
Target Cell Name: U87 MG
Assay Type: Detection of Apoptosis Assays
Assay Overview
This assay is to provide U87 MG-based In Vitro Caspase Activation-based Apoptosis Assay (FCM) to accelerate our client's oncology projects. The assay will be customized according to the specific requirements. Please contact our scientists to discuss more details.
Target Cell Name
U87 MG
Target Cell Organism
Human
Target Cell Background
U-87 MG is a cell line with epithelial morphology that was isolated from malignant gliomas from a male patient, likely with Glioblastoma. Use these cells in your neuroscience and immuno-oncology research.
Target Cell Alternative Name
U87MG; U-87 MG
Related Diseases
Glioblastoma
Research Area
Oncology
Assay Name
In Vitro Caspase Activation-based Apoptosis Assay (FCM)
Short Description
U87 MG-cell based In Vitro Caspase Activation-based Apoptosis Assay (FCM)
Assay Description
Activation of caspases in cancer cells can also be detected by FCM using caspase-specific short peptides linked with a fluorophore. For example, when rhodamine 110 (green fluorescent dye)-linked caspase-specific peptide is attached to protein caspase, its fluorescence is quenched and can be detected by FCM. Fluorochrome-labeled inhibitor of caspase assay (FLICA) is another method used for the detection of apoptosis. Here, fluorylmethyl ketone and carboxyfluorescein are attached at both the ends of a peptide specific to caspase. Upon binding with caspase proteins, it is cleaved and fluoryl methyl ketone prevents further activity by binding with its active sites and finally fluorescence signals will build up in cells.
Assay Type
Detection of Apoptosis Assays
Assay Type Details
Apoptosis (programmed cell death) plays a vital role in embryonic development, homeostasis, functioning of immune system and wound repair. The ability to evade induction of apoptosis has been used by cancer cells to survive against host defense mechanisms. The molecular mechanisms involved in cancer cell apoptosis have been well documented and it involves certain biochemical events such as DNA fragmentation, chromatin condensation, cell organelle degradation and protein cleavage, etc. The extrinsic and intrinsic (mitochondrial) pathways are the two major pathways involved in apoptosis. With the available techniques and assays, a number of apoptosis inducing agents (natural compounds, synthetic compounds, nano-formulations, peptides and enzymes) in many cancer cells have been identified. Selection of an assay for apoptosis detection is based on factors such as apoptotic pathway, nature of drug, cell type being used and the method of analysis.