
Caspase-2–selective tools
The scientific case
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Distinct biology you can’t decipher see with pan-caspase tools.
Caspase-2 (Casp2) regulates synaptic function (AMPA-receptor trafficking), and dementia-related pathogenic signals (tau cleavage, amyloid-beta signaling), neuronal survival under stress, genome-integrity checkpoints (extra-centrosome surveillance), metabolic/ER-stress responses, and retinal ganglion cell death. If you use non-selective inhibitors or generic substrates, you blur Casp2 with Casp3/7/8 and lose mechanistic signal.
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Actionable across multiple fields
Neuroscience (AD/FTD/tauopathies, memory), ophthalmology (RGC protection), oncology (chromosomal instability pathways), hepatology/metabolism (lipotoxic stress, NASH), and ischemia models.
The practical case
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Selectivity = clarity
Our reagents are engineered to maximize discrimination versus executioner caspases (3/7) and inflammatory caspases (1/4/5). That means cleaner readouts, fewer false leads, and data you can defend in manuscripts, diligence, and IND-enabling packages.
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Faster decisions
Pair our fluorogenic Casp2-selective AMC substrates with our Casp2 inhibitors to run rapid MoA confirmation, SAR ranking, and target-engagement/competition assays on a plate reader—no special hardware required.
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Translationally minded
The same chemistry principles underlie our activity-based probe and our therapeutic inhibitor series, so your tool data maps naturally to drug discovery hypotheses.
What we offer
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Use cases: target validation, pathway dissection, rescue experiments, chemical genetics, lead profiling (tool-versus-therapeutic benchmarking).
What you get:
High-purity small molecules (CoA with purity and identity).
Recombinant caspase panel selectivity (datasheet), IC₅₀ or kinact/KI where applicable.
DMSO-friendly stocks; buffer recommendations and ready-to-run protocols.
Optional bundle with matched substrate/probe for immediate TE (target engagement).
Inactive control
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Why AMC? Real-time kinetic readouts (Ex/Em ≈ 350/440 nm) on any standard plate reader; ideal for HTS, enzyme kinetics (KM, kcat), and cell/lysate assays.
What you get:
Optimized tetrapeptide recognition structure (peptidomimetic derivated from pentapeptide) for Casp2 selectivity (reduces cross-talk with Casp3/7).
Validated linear range, guidance for screening, and interference controls.
Protocols/advice for: purified enzyme, cell lysate, and live-cell compatible workflows.
All products are for Research Use Only (RUO). Not for diagnostic or clinical use.
What makes IPcure different
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Designed for Casp2, not “pan-caspase with hopes.” You get an order-of-magnitude selectivity window vs. major off-targets (see datasheets).
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Every shipment includes: CoA, QC traces, panel data summary, step-by-step protocols, and troubleshooting notes.
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We provide lot-to-lot comparability, recommended controls (positive/negative, pan-caspase benchmarking).
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Tools validated in vitro, in cellulo, and in vivo (where applicable) help you move from mechanism to models to partnering conversations without swapping targets or assays.
Buying options
Casp2i™
(small vial: frozen solution at 10mM or lyophilized powder 1-5 mg) + protocols + control recommendations.
Casp2ci™
inactive control inhibitor (small vial: frozen solution at 10mM or lyophilized powder 1-5 mg) + protocols + control recommendations.
Casp2-AMC™
(small vial: frozen solution or lyophilized powder 1-5 mg)
Starter Kit
1× Casp2i™ (small vial) + 1× Casp2-AMC™ + protocols + control recommendations.
Custom & bulk
Quote on request (POs, academic pricing, framework agreements available).
Performance, QC & support
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≥95% (HPLC) with full MS; water and residual solvent specs.
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Recombinant caspase panel and orthogonal protease screen (summary on datasheet).
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DMSO stock; validated buffers (pH/ionic strength), detergent tolerances, and recommended cell media conditions.
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CoA, SDS, protocols, reference list.
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Scientist-to-scientist help in <48 h (method setup, data interpretation, custom requests).
How to get started
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