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TMCB(CK2 and ERK8 Inhibitor): Unlocking New Paradigms in ...
2025-09-25
Explore how the tetrabromo benzimidazole derivative TMCB(CK2 and ERK8 inhibitor) enables a new frontier in biochemical reagent development for protein interaction studies. This article uniquely addresses its role as a molecular tool for dissecting enzyme-driven phase separation with advanced mechanistic insights.
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TAK-242 (Resatorvid): Precision TLR4 Inhibition in Microg...
2025-09-24
Explore how TAK-242, a selective TLR4 inhibitor, enables targeted modulation of microglia polarization and inflammatory pathways in neuropsychiatric and ischemic stroke models. This article delivers an advanced mechanistic analysis and strategic application insights beyond standard reviews.
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Triptolide: Mechanisms of Transcriptional Inhibition in C...
2025-09-23
Explore the multifaceted mechanisms of Triptolide, a potent IL-2 and MMP inhibitor, in transcriptional regulation, cancer research, and developmental biology. This article provides a rigorous analysis of Triptolide’s roles, including its impact on zygotic genome activation and its utility as a tool in elucidating transcriptional networks.
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ABT-199 (Venetoclax) in Mitochondrial Apoptosis: Insights...
2025-09-22
Explore the mechanistic role of ABT-199 (Venetoclax), a selective Bcl-2 inhibitor, in dissecting mitochondrial apoptosis pathways and its implications for non-Hodgkin lymphoma and AML research. This article provides a rigorous synthesis of recent findings and new directions for apoptosis assay development.
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Enhancing Precision Genome Editing with EZ Cap™ Cas9 mRNA...
2025-09-19
Explore how EZ Cap™ Cas9 mRNA (m1Ψ), a capped Cas9 mRNA for genome editing, advances the specificity, stability, and translational efficiency of CRISPR-Cas9 genome editing in mammalian cells, with insights from recent mechanistic studies.
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EZ Cap™ EGFP mRNA (5-moUTP): Advancements in Reporter mRN...
2025-09-18
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br The future of cancer therapeutics with Aurora kinase inhi
2025-04-22
The future of cancer therapeutics with Aurora kinase inhibitors Involvement of Aurora kinases in deregulating multiple tumor suppressor and oncogenic pathways together with the preclinical findings on the efficacy of Aurora kinase inhibitors in attenuating growth of tumor 2X Taq PCR Master Mix (w
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Preliminary results of studies sponsored by the
2025-04-19
Preliminary results of studies sponsored by the manufacturer of ETC-1002 have also shown positive results for monotherapy in statin-intolerant patients and for the combined use of the ACL inhibitor plus other cholesterol-reducing agents. In patients with a documented history of intolerance to statin
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As shown in B the recombinant human
2025-04-18
As shown in B, the recombinant human 15-LOX-1 (30nM) showed a time-dependent increase in fluorescent signal, and signal development was almost completed within 20min in the presence of 50μM arachidonic 2X Taq PCR Master Mix (with dye) and 5μM DHR. For both purified enzyme and cell lysates, the enzy
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Aprotinin In the case of DIA CN
2025-04-18
In the case of DIA-4CN the docking results do not show any interaction between the iron atom and the inhibitor, presumably due to the reduced ability to form a complex involving the -CONN- moiety versus the bidentate -CONHNH- central group of HYD-4Me. This results in a considerable gap between the i
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Of the many different types of DNA lesions
2025-04-17
Of the many different types of DNA lesions, DNA double strand breaks (DSBs) are amongst the most deleterious. It has been suggested that a single unrepaired DSB may be sufficient to induce cell death (Bennett et al., 1993), whereas misrepaired DSBs can result in loss of genetic information, potentia
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Thymoquinone TQ is the major active compound derived from
2025-04-16
Thymoquinone (TQ) is the major active Prestained Protein Marker (Triple color, EDTA free, 10-250 kDa) derived from Nigella sativa (Woo et al., 2012). Recent animal studies support the potential of TQ for the treatment of a variety of inflammatory disorders like inflammatory bowel disease (IBD), RA,
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Crystal structures were obtained of sulfonamide and
2025-04-16
Crystal structures were obtained of sulfonamide 18 and amide 19 as a derivative of amide 36 (Fig. 7A and B). The precise rotameric orientation of amide 36 was of significant interest to understand the compound's interaction with the protein. As it would be difficult to assign the rotomer of 36, the
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We demonstrated clearly that the
2025-04-12
We demonstrated clearly that the overexpression of sFlt-1 significantly increased arginase InstaBlue Protein Stain Solution and enhanced arginase activity in HUVECs (Fig. 3). NO formation is related inversely to serum levels of sFlt-1 in preeclampsia [11]. The disorder of NO formation, which was inv
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br Apelin Discovered in apelin was initially identified as t
2025-04-10
Apelin Discovered in 1998, apelin was initially identified as the sole endogenous ligand for the APJ receptor (Tatemoto et al., 1998). Apelin-77 (pre-pro-apelin) is the precursor for various pharmacologically active apelin isoforms (e.g. apelin-12, -13, -17 and 36), and it shares 75–95% sequence