VASP (phospho-Ser157) Antibody
- Known as:
- VASP (phosphorilated-Ser157) Antibody
- Catalog number:
- abx000265
- Product Quantity:
- EUR
- Category:
- -
- Supplier:
- Abbexa
- Gene target:
- VASP (phospho-Ser157) Antibody
Related genes to: VASP (phospho-Ser157) Antibody
- Gene:
- VASP NIH gene
- Name:
- vasodilator stimulated phosphoprotein
- Previous symbol:
- -
- Synonyms:
- -
- Chromosome:
- 19q13.32
- Locus Type:
- gene with protein product
- Date approved:
- 1996-06-07
- Date modifiied:
- 2017-06-13
Related products to: VASP (phospho-Ser157) Antibody
Related articles to: VASP (phospho-Ser157) Antibody
- The refractory nature of diabetic foot ulcers (DFUs) stems from persistent immunometabolic dysregulation. Although a myriad of reviews have extensively categorized hydrogel dressings, most remain confined to passive material classifications and isolated phenotypic targets. To bridge this gap, this review delineates an integrated "hydrogel engineering-immunometabolic regulation-tissue regeneration" framework. We redefine hydrogels as "intelligent bioreactors" that actively construct a "pro-healing niche," dissecting the underlying mechano-metabolic crosstalk (e.g., VASP/HIF-1α and mTOR signaling). Furthermore, we elucidate the interventional mechanisms of diverse hydrogel strategies-including externally triggered, dynamically responsive, nanocomposite, and mechanically programmed platforms-across four critical pathways: glycolysis, lipid metabolism, amino acid metabolism, and oxidative stress. Crucially, by extracting raw healing data to calculate relative improvement rates and daily relative improvement rates, we quantitatively benchmark the discrepancies in healing kinetics among distinct strategies. Building upon this, we propose scenario-oriented clinical selection pathways: prioritizing near-infrared (NIR)-responsive or photocatalytic hydrogels for severely hypoxic DFUs, and recommending ultrasound-driven sequential "sterilization-then-antioxidation" hydrogels for neuropathic ulcers complicated by multidrug-resistant bacterial infections. Additionally, via precise metabolic reprogramming, these tailored hydrogels actively drive macrophage repolarization, restore T cell subset balance, and enhance dendritic cell efferocytosis. Finally, by integrating biomarker-driven standardized evaluations, GMP-compliant scale-up engineering, and AI-assisted modular production platforms, this review outlines a step-by-step clinical translational roadmap. This strategic roadmap aims to bridge the gap between laboratory prototypes and personalized precision medicine, ultimately providing a comprehensive blueprint for next-generation metabolic therapeutics in chronic wound management. - Source: PubMed
Publication date: 2026/06/19
Xu ZimingYang ZongtongLiu RuiWang YutaoLi YufeiSun Qing - Scanning tunneling microscopy was used to investigate the arrangement of ferrocenecarboxylic acid (FcCOOH) monolayers on the Ag(111) surface. Four distinct structures were observed, none of which had previously been observed on other surfaces. Structural analysis indicates that these assemblies are primarily composed of dimers. VASP calculations support the molecular assignments of the monolayer structures, while ESI-MS experiments confirm that dimers are the predominant species in solution. Of particular note, the cyclic pentamers and aperiodic packing observed for FcCOOH on Au(111) were not observed, despite (1) the similarity of the Ag(111) and Au(111) surfaces in reactivity, flatness, and lattice constant, and (2) prior explanation of the Au(111) monolayer in terms of molecule-molecule interactions alone. It is clear that while the surface does not have a template structure, it has a significant influence on which structures are formed. - Source: PubMed
Publication date: 2026/06/24
Heiner Benjamin RHandy Kaitlyn MWalter Alex LPetersen Jacob PKandel S Alex - Predicting tensorial properties with machine learning models typically requires carefully designed tensorial descriptors. In this work, we introduce an alternative strategy for learning tensorial quantities based on scalar descriptors. We apply this approach to the Born effective charge tensor, showing that scalar (monopole) kernel models can successfully capture its tensorial nature by exploiting the definition of the Born effective charge tensor as the derivative of the polarization with respect to atomic displacements. We compare this method with tensorial (dipole) kernel models, as established in our previous work, in which the tensorial structure of the Born effective charge is encoded directly in the kernel and obtained via its derivative. Both approaches are then used for charge partitioning, enabling the separation of monopole and dipole contributions. Finally, we demonstrate the effectiveness of the framework by computing finite-temperature infrared spectra for a range of complex materials. - Source: PubMed
Schmiedmayer BernhardRittsteuer AngelaHilpert TobiasKresse Georg - In this study, an expanded graphite/paraffin-based phase change material (PCM) was efficiently and sustainably prepared via a low-temperature synchronous expansion-adsorption method. The mechanism was further elucidated utilizing FTIR, SEM, BET, XPS, XRD, TG-DSC, and VASP simulation calculations. The results indicate that since paraffin adsorption occurs during graphite expansion, it better adsorbs into the interstitial spaces of expanded graphite, further enhancing its leak resistance while improving thermal conductivity (0.20 W/(m·K)). The EG:Paraffin = 1:4 sample exhibits minimal pore volume (0.002667 cm), indicating the fewest surface pores on the phase change material, demonstrating effective paraffin adsorption. Simultaneously, without excessive paraffin adsorption, the EG:Paraffin = 1:4 sample exhibited the lowest total weight loss at 71.3%. The interlayer spacing of expanded graphite was effectively increased at low temperatures, resulting in a final expansion volume of 203 mL/g. Throughout the system, the characteristic wax peaks remained distinctly present, indicating that the composite process between expanded graphite and wax was a physical mixture. This finding is consistent with both the XPS spectra and simulation calculations. This study provides an innovative method with greener, more energy-efficient, simplified preparation process to obtain the freshly synthesized porous graphite for the synchronous integration with PA, which can facilitate the rapid development of controllable microstructure and large-scale production of EG/PA-based composite PCMs. - Source: PubMed
Publication date: 2026/06/02
Yang HangZhang YunhaiCui BaoyuLi WeiguangZhao Qingchao - The development of two-dimensional van der Waals heterostructures for optoelectronic and photocatalytic applications demands precise control over band alignment and light absorption. This study addresses the challenge of engineering strain-tunable electronic properties in the MoSiN/WSSe heterostructure, a system exhibiting intrinsic type-I band alignment and a direct band gap of 1.850 eV. We demonstrate that interfacial charge transfer of 0.0831 |e| from MoSiN to WSSe generates a robust internal electric field, significantly enhancing charge separation and transport. Crucially, compressive strain induces reversible transitions between type-I and type-II band alignments and between direct and indirect band gaps, enabling dynamic modulation of carrier dynamics. At -4% and -5% strain, the charge transfer aligns with the Z-scheme characteristics, and band edges positions precisely match the water redox potentials. Compared with its individual monolayer components, the heterostructure demonstrates enhanced optical absorption across both visible and ultraviolet spectral regions. Tensile strain markedly enhances light absorption, with the absorption coefficient peak increasing from 5.4 to 28.5%, and induces a redshift of the absorption peak in the visible light range. These findings confirm that the MoSiN/WSSe heterostructure, with its excellent tunability, holds considerable promise for applications in optoelectronic and photocatalytic devices based on thermodynamic band alignment. - Source: PubMed
Publication date: 2026/06/19
Li JianwenLi JieLiu ZixuXu Chengyong