Hep55.1c In Vitro Annexin V-based Apoptosis Assay (FCM)
CAT#: ITS-0123-YF39
Target Cell Organism: Mouse
Target Cell Name: Hep55.1c
Assay Type: Detection of Apoptosis Assays
Assay Overview
This assay is to provide Hep55.1c-based In Vitro Annexin V-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
Hep55.1c
Target Cell Organism
Mouse
Target Cell Background
The Hep55.1C cell line is derived from carcinogen-induced liver tumors of C57BL/6 mice and utilized in a syngeneic orthotopic murine model of HCC.
Related Diseases
Hepatocellular Carcinoma
Research Area
Oncology
Assay Name
In Vitro Annexin V-based Apoptosis Assay (FCM)
Assay Description
Localization of phosphatidyl serine, a phospholipid found normally in the internal surface of the plasma membrane, to the external surface of the plasma membrane occurs during apoptosis. Annexin V can bind with phosphatidyl serine and Annexin V conjugates (Annexin V/fluorescein isothiocyanate) are commonly used for detecting apoptosis by FCM.
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.