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ApoBrite™ U470 caspase 3/7 substrate *Cell-Permeable*

Mechanism for ApoBrite™ U470 caspase substrate. Cell-permeable functional group allows probe to enter live cell. Once inside the cell, the caspase selective peptide is cleaved by caspase to reveal the masked fluorophore.
Mechanism for ApoBrite™ U470 caspase substrate. Cell-permeable functional group allows probe to enter live cell. Once inside the cell, the caspase selective peptide is cleaved by caspase to reveal the masked fluorophore.
Mechanism for ApoBrite™ U470 caspase substrate. Cell-permeable functional group allows probe to enter live cell. Once inside the cell, the caspase selective peptide is cleaved by caspase to reveal the masked fluorophore.
The fluorescence microscope images of normal Hela cells (A) and apoptotic Hela cells (B). Hela cells were cultured in a 96-well plate, and washed twice with HHBS buffer. ApoBrite™ U470 caspase 3/7 dye loading solution was then added to the well. After incubation for 2 h at 37 °C, the cells were washed once with HHBS buffer and treated with staurosporine (1 μM) apoptosis inducer for 1 hr. The images were acquired using a fluorescence microscope equipped with DAPI filter set.
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Physical properties
SolventDMSO
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12352200

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ApoBrite™ U470 is our recently developed cell-permeable fluorogenic caspase substrate, the first fluorogenic probe for the direct detection of caspase activities in live cells. ApoBrite U470 consists of three moieties including a). masked fluorophore, b). caspase-selective peptide fragment (DEVD), and c). cell-penetrating moiety. The cell-penetrating moiety carries the probe into live cells. Upon entering live cells the caspase-selective peptide fragment is cleaved by a caspase to release the masked fluorophore. The intensity of recovered fluorescence is directly related to the activity of caspase to be measured. Compared to the existing caspase assays in live cells, ApoBrite™ U470 is much more robust, convenient and accurate. It does not need a DNA interaction to be fluorescent as reported for NucView reagents. It does not inhibit caspase activity as reported for the FMK peptide probes. Although fluorescent FMK peptide inhibitors of caspases are widely used for detecting caspase activities in live cells, this technology has a few severe limitations: a). FMK caspase inhibitors have high cytotoxicity since FMK peptides bind covalently to active caspases; b). The irreversibly covalent binding of FMK peptides to caspases inhibits caspase activities, causing false positive apoptosis; c). FMK assays have extremely high background, and require intensive washings, resulting in very low through put; d). FMK peptides are not stable in aqueous solutions, and have to be used immediately.

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Citations


View all 3 citations: Citation Explorer
Helicobacter pylori Secreted Protein HP1286 Triggers Apoptosis in Macrophages via TNF-Independent and ERK MAPK-Dependent Pathways
Authors: Tavares, Raquel and Pathak, Sushil Kumar
Journal: Frontiers in Cellular and Infection Microbiology (2017): 58
Death receptor 3 mediates necroptotic cell death
Authors: Bittner, Sebastian and Knoll, Gertrud and Ehrenschwender, Martin
Journal: Cellular and Molecular Life Sciences (2016): 1--12
Helicobacter pylori protein JHP0290 exhibits proliferative and anti-apoptotic effects in gastric epithelial cells
Authors: Tavares, Raquel and Pathak, Sushil Kumar
Journal: PloS one (2015): e0124407

References


View all 50 references: Citation Explorer
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Journal: Eur Arch Otorhinolaryngol (2011): 987
In vitro effect of different mediators of apoptosis on canine cranial and caudal cruciate ligament fibroblasts and its reversibility by pancaspase inhibitor zVAD.fmk
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