aCella - Tox - an assay designed to measure cell cytoxicity
A bioluminescence, non-radioactive cytotoxicity assay designed to quantitatively measure the release of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) from mammalian cell lines or bacterial cells.
Product Specifications
Label
ICT
Cell Type
Ramos cells; Daudi Cells
Type
Cell Viability
Detection Method
Luminometer
Assay Protocol
https://cdn.shopify.com/s/files/1/0512/5793/4009/files/aCella-TOX_v1_3_Protocol.pdf?v=1679588911
Components
1. 4X Enzyme Assay Reagent Part# 6001 x 1 (Storage: -20°C), 2. Enzyme Assay Diluent Part# 3008 x 1 (Storage: 2-8°C), 3. 50X Detection Reagent Part# 6002 x 1 (Storage: -20°C), 4. 5.5X Detection Assay Diluent Part# 3009 x 1 (Storage: -20°C), 5. Glyeraldehyde 3-Phosphate-G3P Part# 6003 x 1 (Storage: -20°C), 6. Lysis Buffer Part# 3035 x 1 (Storage: 2-8°C),
Shipping Conditions
Ships overnight (domestic), International Priority Shipping
Storage Temperature
Store contents as labeled
Target Description
GAPDH is an important enzyme in the glycolysis and gluconeogenesis pathways. This homotetrameric enzyme catalyzes the oxidative phosphorylation of D-glyceraldehyde-3-phosphate to 1,3-diphosphoglycerate in the presence of cofactor and inorganic phosphate. In the aCella-TOX reaction scheme the release of GAPDH is coupled to the activity of the enzyme 3-Phosphoglyceric Phosphokinase (PGK) to produce ATP. ATP is detected via the luciferase, luciferin Bioluminescence methodology. Further, aCella-TOX is a homogeneous cytotoxicity assay; alternatively in dual mode, aCella-TOX can measure cytotoxicity and cell viability in the same plate. Culture supernatants can also be removed from the original plate and assayed in a different plate, allowing kinetics runs to be set up. The assay is non-destructive, allowing the monitoring of additional parameters such as gene expression.
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