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Auranofin: Advanced Redox Modulation and Cytoskeletal Cro...
2025-09-30
Explore how Auranofin, a potent thioredoxin reductase inhibitor, uniquely disrupts redox homeostasis while intersecting with cytoskeletal autophagy for next-generation cancer and antimicrobial research. Uncover mechanistic insights and innovative applications beyond conventional approaches.
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Protease Inhibitor Cocktail EDTA-Free (100X): Precision i...
2025-09-29
Explore the advanced science and unique advantages of Protease Inhibitor Cocktail EDTA-Free (100X in DMSO) for phosphorylation-sensitive protein extraction. This in-depth guide reveals mechanistic insights, practical optimization, and breakthrough applications beyond standard protocols.
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Triptolide: Unraveling Transcriptional Control and Plurip...
2025-09-28
Explore how Triptolide redefines transcriptional inhibition in cancer and developmental biology. This in-depth analysis uniquely connects Triptolide’s CDK7-mediated RNAPII degradation and matrix metalloproteinase inhibition with pluripotency network rewiring, offering fresh insights for advanced cancer and rheumatoid arthritis research.
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TCEP Hydrochloride: Pioneering Precision Redox Chemistry ...
2025-09-27
Explore how Tris(2-carboxyethyl) phosphine hydrochloride (TCEP hydrochloride) revolutionizes protein structure analysis, redox biochemistry, and synthetic workflows as a water-soluble reducing agent. This in-depth guide reveals advanced mechanisms and next-generation applications overlooked by standard protocols.
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DAPI (hydrochloride) in Organoid Systems: Decoding Stem C...
2025-09-26
Explore the unique role of DAPI (hydrochloride) as a fluorescent DNA stain for dissecting cellular diversity and lineage dynamics in advanced organoid models. This cornerstone article reveals how DAPI empowers researchers to unravel the interplay between stem cell self-renewal and differentiation, offering scientific insights beyond standard protocols.
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KU-60019: Exploiting ATM Kinase Inhibition for Metabolic ...
2025-09-25
Explore how KU-60019, a selective ATM kinase inhibitor, unlocks metabolic synthetic lethality in glioma models by targeting DNA damage response and macropinocytosis. Discover unique applications and advanced therapeutic strategies for cancer research.
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3X (DYKDDDDK) Peptide: Next-Generation Tag for Quantitati...
2025-09-24
Discover how the 3X (DYKDDDDK) Peptide unlocks advanced affinity purification and immunodetection of FLAG fusion proteins, with a special focus on quantitative proteomics and decoding ubiquitin signaling. Explore novel mechanisms, metal-dependent ELISA assay innovation, and future directions in protein research.
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DAPI (hydrochloride): Unraveling DNA Dynamics in Organoid...
2025-09-23
Explore the versatile applications of DAPI (hydrochloride) as a DNA-specific fluorescent probe for flow cytometry and organoid research. This article delves into how DAPI enables high-resolution analysis of cell cycle dynamics and lineage diversification in advanced intestinal organoid systems.
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In this study for the first instant we report the
2025-03-03

In this study, for the first instant we report the characterization, production and in silico structural analysis of BADH1 gene in B. haloduranss SMBPL06 isolated from the salt pan. Moreover, the sequence analysis of betaine aldehyde dehydrogenase from B. haloduranss SMBPL06 displayed several base s
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Some alterations in the integrity
2025-03-03

Some alterations in the integrity of cell membranes caused by toxic agents can be determined by measuring certain enzymes released by damaged cells [8]. The cholinesterases, for example, catalyze the hydrolysis of R 568 hydrochloride (ACh) in choline and acetic acid. Theses enzymes are divided into
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br Funding br Introduction l Dihydroxyphenylalanine l DOPA
2025-03-03

Funding Introduction l-3,4-Dihydroxyphenylalanine (l-DOPA) is the gold-standard treatment for the motor symptoms of Parkinson's disease (PD); however, its chronic use induces severe motor complications that eventually limit its long-term efficacy (Bastide et al., 2015). The most disabling side
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Nevertheless though the LO pathway dictates the
2025-03-03

Nevertheless, though the 5-LO pathway dictates the production of lipid mediators with opposite roles in the immune reactions, like LTs and LXA4 [32], our results seemed to corroborate others that pointed to LTB4 as an outstanding mediator involved in persistent and chronic inflammatory skin diseases
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br Conclusion To conclude it would be
2025-03-03

Conclusion To conclude, it would be fair to say that the research efforts on FLAP inhibitors for intervening with LT biosynthesis have reached to a considerably advanced state during the last decade as a result of growing interest from both pharmaceutical industry and academia [4], [37], [38]. Du
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Jesus et al discovered a
2025-03-03

Jesus et al. discovered a new series of azaindole as Aurora inhibitors through various modification of GSK1070916 (47). They synthesized series from modification of the GSK1070916 and evaluated for in-vitro Aurora-B/INCENP and Aurora-A/TPX2 inhibition assays. Modified cy5 dye 48 and 49 showed IC50
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The amino hydroxy methyl isoxazolepropionic acid
2025-03-01

The α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic Gastroprokinetic agent antagonist (AMPA) receptor is also enriched in postsynaptic striatal neurons (Bernard et al., 1997, Kondo et al., 2000, Reimers et al., 2011). Its activity is subjected to the regulation by a mechanism involving phosphorylat
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