Key features and details
- Assay type: Quantitative
- Detection method: Fluorescent
- Platform: Microplate reader
- Assay time: 1 hr 30 min
- Sample type: Adherent cells, Suspension cells
Product nameCaspase-7 Inhibitor Assay Kit
Sample typeAdherent cells, Suspension cells
Assay time1h 30m
Abcam's Caspase 7 Inhibitor Drug Detection Kit provides an effective means for screening caspase inhibitors using fluorometric methods. The assay utilizes synthetic peptide substrate DEVD-AFC (AFC, 7-amino-4-trifluoromethyl coumarin). Active caspase 7 cleaves the synthetic substrate to release free AFC which can then be quantified by fluorometry. Compounds to be screened can directly be added to the reaction and the level of inhibition of caspase 7 activity can be determined by comparison of the fluorescence intensity in samples with and without the testing inhibitors.
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Caspases have been shown to play a crucial role in apoptosis induced by various deleterious and physiologic stimuli. Inhibition of caspases can delay apoptosis, implicating a potential role in drug screening efforts.
Storage instructionsStore at -20°C. Please refer to protocols.
Components 100 tests 2X Reaction Buffer 1 x 10ml Active Caspase-7 1 x 100 units Caspase Inhibitor, Z-VAD-FMK 1 x 10µl Caspase Substrate DEVD-AFC 1 x 0.5ml DTT 1 x 100µl
RelevanceCaspases have been shown to play a crucial role in apoptosis induced by various deleterious and physiologic stimuli. Inhibition of caspases can delay apoptosis, implicating a potential role in drug screening efforts.
- CASP7 inhibitor
Caspase activity (RFU) in presence of 0µM - 40µM of z-VAD-FMK (generic caspase inhibitor), assessed using DEVD-AFC as caspase substrate and following Caspase 7 Inhibitor Drug Detection Kit (ab102495) protocol. Lanes:
1.- Background Control: no Caspase 7, no z-VMAD-FMK
2.- Positive Inhibition Control: no Caspase 7, +z-VAD-FMK
3.- Positive Control: + Caspase 7, no z-VAD-FMK
4.- Caspase 7 + 2.5µM z-VAD-FMK
5.- Caspase 7 + 10µM z-VAD-FMK
6.- Caspase 7 + 40µM z-VAD-FMK
ab102495 has not yet been referenced specifically in any publications.