Rat Anti-Mouse CD202b
- Known as:
- Rat Antibody toMouse CD202b
- Catalog number:
- 129-10118
- Product Quantity:
- 25
- Category:
- -
- Supplier:
- Ray Biotech
- Gene target:
- Rat Anti-Mouse CD202b
Ask about this productRelated genes to: Rat Anti-Mouse CD202b
- Gene:
- TEK NIH gene
- Name:
- TEK receptor tyrosine kinase
- Previous symbol:
- VMCM
- Synonyms:
- TIE2, TIE-2, VMCM1, CD202b
- Chromosome:
- 9p21.2
- Locus Type:
- gene with protein product
- Date approved:
- 1994-05-24
- Date modifiied:
- 2018-08-07
Related products to: Rat Anti-Mouse CD202b
Related articles to: Rat Anti-Mouse CD202b
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Publication date: 2026/06/10
Sato YuWignakumar AnjelliRogers PeterValdivieso CesarHambleton MichelleMoola MohammedBilotti MatthewBarnes SpencerPerrone CameronSipe SamanthaAbraham AbelLopez Christopherda Silva GiovannaWexner Steven D - This study sought to elucidate the antitumor mechanisms of the traditional herbal combination Astragalus-Curcuma zedoaria (A-C) in lung squamous cell carcinoma (LUSC). Drug-containing serum was prepared from mice administered an A-C decoction, and serum-absorbed bioactive components were identified using high-resolution mass spectrometry. To investigate potential targets and pathways within the tumor immune microenvironment, network pharmacology analysis was integrated with bulk transcriptomic data from TCGA-LUSC and single-cell RNA sequencing (scRNA-seq). The analytical methodologies employed included differential gene expression analysis, weighted gene co-expression network analysis (WGCNA), functional enrichment analysis, and molecular docking. The scRNA-seq data identified 22 distinct cell clusters, with correlation analysis suggesting that A-C primarily exerts its effects through vascular endothelial cells. Among the serum-derived components, demethoxycurcumin-a principal curcuminoid from C. zedoaria-demonstrated the highest binding affinity with the TEK receptor tyrosine kinase (-7.5 kcal/mol), indicating its potential role in modulating endothelial function and vascular-immune interactions. In conclusion, the A-C combination exhibits a synergistic effect in lung squamous cell carcinoma (LUSC) by modulating differentially expressed genes, with demethoxycurcumin identified as a pivotal bioactive compound targeting TEK. These results elucidate novel dual antitumor mechanisms of the A-C herbal pair, achieved through the regulation of the vascular-immune microenvironment. - Source: PubMed
Yu LuhangDong XueshanYang QianyuDou Yongqi - This retrospective study aimed to evaluate anesthesia management, intraoperative support strategies, and 60-day clinical outcomes in patients requiring surgical intervention, including fasciotomy and/or amputation, due to crush and compartment syndrome following the February 6, 2023, Kahramanmaraş earthquakes. The study also sought to identify predictors of mortality and contribute to the field of disaster medicine. - Source: PubMed
Taygurt Tugba NurErdem GökhanTaygurt SüleymanKoç Muhammed Nezih - Early-onset appendiceal cancer (EOAC), diagnosed before age 50, accounts for approximately 30% of all appendiceal malignancies. Its clinical profile, treatment strategies, and outcomes remain underexplored compared to late-onset disease. This study aimed to assess demographics, disease profile, management, and outcomes of EOAC. - Source: PubMed
Publication date: 2026/06/05
Emile Sameh HanyWignakumar AnjelliGaroufalia ZoeWexner Steven D - The sluggish kinetics of the oxygen reduction reaction (ORR) and the high cost of Pt-based catalysts remain major barriers for alkaline fuel cell (AFC) technologies. Here we report a Cu-decorated CoO@Pd catalyst in which atomic-to-subnanometer CuO species reconstruct the Pd-Co-Cu heterointerface and enable a cooperative multi-site ORR pathway. Structural and spectroscopic analyses reveal that low Cu loading produces atomically dispersed CuO motifs that enrich oxygen vacancies (O)s, preserve metallic Pd, and stabilize oxygen-deficient Co centers. Operando PFY-XANES/EXAFS further uncovers a synergistic mechanism in which Os around Cu serve as rapid O activation sites, Pd mediates lateral *O spillover, and Os around Co act as the primary *O reduction centers. This division of labor maximizes four-electron ORR kinetics, yielding a on-set potential of 0.935 V and a mass activity (MA) of ∼1.6 × 10 mA mg without decay for 50k potential cycles, surpassing commercial Pt/C by over two orders of magnitude. When integrated into AFCs, the optimized catalyst (CPCu-1) delivers a peak power density of ∼430 mW cm , approximately 60% higher than Pt/C, and exhibits a characteristic three-stage durability governed by dynamic CuO-CoO interface reconstruction. These findings establish atomic CuO interface engineering strategy for designing high-performance, noble-metal-efficient ORR catalysts. - Source: PubMed
Publication date: 2026/06/04
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