Archives
- 2026-02
- 2026-01
- 2025-12
- 2025-11
- 2025-10
- 2025-09
- 2025-03
- 2025-02
- 2025-01
- 2024-12
- 2024-11
- 2024-10
- 2024-09
- 2024-08
- 2024-07
- 2024-06
- 2024-05
- 2024-04
- 2024-03
- 2024-02
- 2024-01
- 2023-12
- 2023-11
- 2023-10
- 2023-09
- 2023-08
- 2023-07
- 2023-06
- 2023-05
- 2023-04
- 2023-03
- 2023-02
- 2023-01
- 2022-12
- 2022-11
- 2022-10
- 2022-09
- 2022-08
- 2022-07
- 2022-06
- 2022-05
- 2022-04
- 2022-03
- 2022-02
- 2022-01
- 2021-12
- 2021-11
- 2021-10
- 2021-09
- 2021-08
- 2021-07
- 2021-06
- 2021-05
- 2021-04
- 2021-03
- 2021-02
- 2021-01
- 2020-12
- 2020-11
- 2020-10
- 2020-09
- 2020-08
- 2020-07
- 2020-06
- 2020-05
- 2020-04
- 2020-03
- 2020-02
- 2020-01
- 2019-12
- 2019-11
- 2019-10
- 2019-09
- 2019-08
- 2019-07
- 2019-06
- 2019-05
- 2019-04
- 2018-11
- 2018-10
- 2018-07
-
Disulfiram: Applied Cancer Research & Proteasome Pathway ...
2026-02-01
Disulfiram, beyond its legacy as an anti-alcoholism drug, is now a precision tool for inhibiting proteasomal activity and inducing apoptosis in cancer research models. Its copper-complexed form unlocks robust experimental workflows, especially in breast cancer studies, while troubleshooting guidance ensures reproducible results. Discover how APExBIO’s Disulfiram bridges traditional pharmacology and next-generation translational science.
-
Scenario-Driven Best Practices for MG-262 (Z-Leu-Leu-Leu-...
2026-01-31
This article delivers scientific, scenario-based guidance for leveraging MG-262 (Z-Leu-Leu-Leu-B(OH)2) (SKU A8179) in cell viability, proliferation, and apoptosis workflows. Drawing on recent literature and real laboratory challenges, we provide actionable strategies for robust, reproducible proteasome inhibition and data interpretation. Researchers will gain practical insight into experimental design, protocol optimization, and reliable vendor selection.
-
Decoding Immunoproteasome LMP7 Inhibition: Strategic Blue...
2026-01-30
This thought-leadership article delivers an integrated analysis of ONX-0914 (PR-957)—a selective immunoproteasome LMP7 inhibitor—with a focus on its mechanistic underpinnings, experimental validation, and translational promise in autoimmune and inflammatory disease research. Drawing on recent peer-reviewed discoveries, including the immunoproteasome's role in IL-4Rα degradation and regulation of type 2 inflammation, we provide strategic guidance for researchers aiming to leverage ONX-0914 for advanced cytokine blockade, disease modeling, and therapeutic innovation. The article also critically positions ONX-0914 (PR-957) from APExBIO within the competitive landscape, highlighting best practices and visionary directions to accelerate impact beyond the current literature.
-
CB-5083: Selective p97 Inhibitor for Protein Homeostasis ...
2026-01-30
CB-5083 is a potent, orally bioavailable selective p97 AAA-ATPase inhibitor. It disrupts protein homeostasis, induces apoptosis in cancer cells, and demonstrates robust tumor growth inhibition in preclinical models. This article provides atomic, verifiable facts and structured evidence for researchers using CB-5083 in multiple myeloma and solid tumor research.
-
PYR-41: Selective Ubiquitin-Activating Enzyme E1 Inhibito...
2026-01-29
PYR-41, a selective inhibitor of Ubiquitin-Activating Enzyme E1, is a robust tool for dissecting ubiquitin-proteasome system dynamics in protein degradation and inflammation models. Its utility is underpinned by well-characterized mechanistic action and reproducible benchmarks in apoptosis and NF-κB signaling pathway modulation. This article provides atomic, verifiable claims to guide rigorous experimental use and clarify common misconceptions.
-
Strategic Disruption of Protein Homeostasis: CB-5083 and ...
2026-01-29
CB-5083, a potent and selective oral p97 AAA-ATPase inhibitor, is redefining the landscape of translational oncology and genome stability research. This thought-leadership article examines the mechanistic underpinnings of p97 inhibition, leverages new insights from DNA repair studies in naked mole-rats, and offers strategic guidance for researchers pursuing next-generation therapies in multiple myeloma and solid tumors. The discussion integrates recent findings, competitive intelligence, and visionary perspectives to chart a bold agenda for the field.
-
CB-5083: Selective p97 AAA-ATPase Inhibitor for Cancer Ce...
2026-01-28
CB-5083 is a potent, orally bioavailable p97 inhibitor that disrupts protein homeostasis and induces apoptosis in cancer cells. This article details its mechanistic specificity, benchmarks, and workflow parameters, positioning CB-5083 as a validated research tool for studying protein degradation pathways and tumor growth inhibition.
-
Reliable Proteasome Inhibition in Cell Assays: MG-262 (Z-...
2026-01-28
Discover how MG-262 (Z-Leu-Leu-Leu-B(OH)2) (SKU A8179) addresses key laboratory challenges in cell viability, proliferation, and apoptosis assays. This scenario-driven guide provides practical, literature-backed insights for biomedical researchers, highlighting workflow optimization and reproducibility using MG-262 for robust proteasome inhibition.
-
MG-132 (SKU A2585): Data-Driven Solutions for Cell Viabil...
2026-01-27
This article delivers a scenario-driven, evidence-based guide to using MG-132 (SKU A2585) for robust cell viability, proliferation, and apoptosis research. Drawing on validated workflows and quantitative data, it addresses common laboratory challenges and compares vendor options, enabling researchers to achieve reproducible results and mechanistic clarity with APExBIO’s reliable MG-132.
-
MG-262 (Z-Leu-Leu-Leu-B(OH)2): Advanced Insights into Rev...
2026-01-27
Explore the multifaceted applications of MG-262, a potent reversible proteasome inhibitor, in the study of protein homeostasis, cell cycle arrest, and disease mechanisms. This article offers advanced analysis on MG-262's role in dissecting the ubiquitin-proteasome system—revealing new opportunities for apoptosis research and translational disease modeling.
-
CB-5083 (SKU B6032): Reliable p97 Inhibition for Reproduc...
2026-01-26
This in-depth article addresses frequent laboratory challenges in cell viability and protein degradation assays, demonstrating how CB-5083 (SKU B6032) from APExBIO delivers consistent, data-driven solutions. The discussion is grounded in quantitative evidence and workflow best practices, helping life science researchers optimize experimental reproducibility, interpret results, and select high-quality reagents for cancer and protein homeostasis research.
-
Topotecan HCl: Precision Modeling of Tumor Cell Fate and ...
2026-01-26
Explore how Topotecan HCl, a potent topoisomerase 1 inhibitor, enables advanced modeling of tumor cell fate, DNA damage, and selective toxicity in preclinical cancer research. This article delivers a unique systems perspective, integrating in vitro evaluation frameworks and translational insights.
-
MG-262 (Z-Leu-Leu-Leu-B(OH)2): Practical Scenarios for Re...
2026-01-25
This article provides biomedical researchers and lab technicians with real-world, scenario-driven guidance on using MG-262 (Z-Leu-Leu-Leu-B(OH)2) (SKU A8179) for sensitive, reproducible proteasome inhibition in cell-based assays. Integrating data-backed answers to common workflow challenges, it clarifies how MG-262 from APExBIO supports robust cell viability, apoptosis, and signaling studies across a range of disease models.
-
MLN2238: Next-Gen Proteasome β5 Inhibitor Fueling Redox S...
2026-01-24
Explore the unique role of MLN2238 as a reversible 20S proteasome β5 subunit inhibitor in modulating redox pathways, apoptosis, and NF-κB suppression for multiple myeloma and lymphoma research. This in-depth analysis reveals novel mechanistic insights and experimental strategies that set MLN2238 apart in hematologic malignancy studies.
-
Topotecan HCl in Translational Cancer Models: Deep Phenot...
2026-01-23
Explore how Topotecan HCl, a leading topoisomerase 1 inhibitor, enables advanced phenotypic profiling and translational research across lung, prostate, and colon cancer models. Unlock new perspectives on mechanism-driven cytotoxicity and tissue-specific toxicity, grounded in the latest in vitro methodologies.