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8 cell viability (apo-one caspase-3/7 assay), Cell viability (apo-one caspase-3/7 assay) – Eppendorf AF2200 Plate Reader User Manual

Page 67

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Predefined methods

Eppendorf

®

PlateReader AF2200

English (EN)

67

6.2.8

Cell viability (Apo-ONE Caspase-3/7 Assay)

Introduction

The Apo-ONE Homogeneous Caspase-3/7 Assay provides a homogenous fluorometric method for
monitoring apoptosis in mammalian cells. The assay is based on the measurement of the activities of the
proteases caspase-3 and -7 in the process of apoptosis. A pro-fluorescent substrate becomes fluorescent
after cleavage by the activated caspases.

Default measurement parameters

• Excitation wavelength: 485 (25) nm

• Emission wavelength: 535 (35) nm

• Number of flashes: 25

• Settle time: 0 ms

• Mode: Top

• Lag time: 0 μs

• Integration: 20 μs

• Gain: "optimal"

• Plate definition: Eppendorf Cell Culture Plate 96/F, black/clear" or comparable plates

User defined method parameters

• The measurement is performed at 485 / 535 nm with default measurement parameters.

• Define the number of blank replicates (possible number: 1 – 6).

• Define the number of control replicates (possible number: 1 – 6).

• Define number of samples and sample replicates (max. 58, depends on number of blanks and controls).

• Define appropriate sample identifier (default settings are ID_1, ID_2, ..).

• Check if entered parameters are correct.

• Required plate layout: Outer wells are left empty by default. Pipette in a vertical order, starting with

blanks at position B2, controls are pipetted in subsequent wells, samples must be placed in the
following wells.

• Press

Start

.

• For method results and data evaluation principle see chapter

method results

and

evaluation procedure

.

The method is restricted to 96-well microplates.
Because of faster evaporation the wells lying on the outer sides of the plate are not included in
the evaluation.
 Please fill them with buffer or distilled water.