Designed to
detect ADP/ATP ratios for a rapid screening of apoptosis/necrosis/growth
arrest/cell proliferation simultaneously in mammalian cells.
Offers highly consistent results and with excellent correlation
to other apoptosis markers (e.g. TUNEL-based assays and caspase
assays). Assay can be fully automatic for high throughput (10
seconds/sample) and is highly sensitive (detects 10-100 cells/well).
Utilizes
bioluminescent detection of the ATP level via luciferase
catalyzed reaction for a rapid screening of apoptosis and cell
viability in mammalian cells. The assay can be done directly in
culture plates requiring no harvest/washing/or sample
preparations and can be fully automatic for high throughput (10
seconds/sample) and is highly sensitive (detects 10-100
mammalian cells/well).
Provides ready-to-use
staining reagents and incubation buffer for distinguishing
between live and dead cells in culture. Contains a cell-permeable
green fluorescent dye (Ex/Em = 490/515 nm) for staining live
cells and propidium iodide (PI Ex/Em = 488/615 nm) for staining
dead cells. Stained lice and dead cells can easily be visualized
by fluorescence microscopy.
This fast and
sensitive assay measures cell proliferation in response to
growth factors/cytokines/mitogens/and nutrients etc. The method
is so simple requiring no washing/harvesting/or solubilization
steps and is faster and more sensitive than MTT/XTT/or MTS-based
assays. The entire assay can be performed directly in a 96-well
plate.
+32
1658 9045
+32
1650 9045
