Mouse Monoclonal to CD105 / Endoglin, Clone MEM-229, Isotype IgG2aApplication FC, WB, IHC(F), ICC Concentration 1 mg/ml
- Known as:
- Mouse Monoclonal CD105 / Endoglin, Clone MEM-229, Isotype IgG2aApplication FC, Western Blot, Immunohistochemistry(F), ICC Concentration 1 mg/milliliter
- Catalog number:
- 1B-453-C025
- Product Quantity:
- 0.025 mg
- Category:
- -
- Supplier:
- Exbio
- Gene target:
- Mouse Monoclonal CD105 / Endoglin Clone MEM-229 Isotype IgG2aApplication IHC() ICC Concentration 1
Related genes to: Mouse Monoclonal to CD105 / Endoglin, Clone MEM-229, Isotype IgG2aApplication FC, WB, IHC(F), ICC Concentration 1 mg/ml
- Gene:
- BIRC3 NIH gene
- Name:
- baculoviral IAP repeat containing 3
- Previous symbol:
- API2
- Synonyms:
- cIAP2, hiap-1, MIHC, RNF49, MALT2, c-IAP2
- Chromosome:
- 11q22.2
- Locus Type:
- gene with protein product
- Date approved:
- 1998-06-10
- Date modifiied:
- 2016-10-05
- Gene:
- ENG NIH gene
- Name:
- endoglin
- Previous symbol:
- ORW1, ORW
- Synonyms:
- END, HHT1, CD105
- Chromosome:
- 9q34.11
- Locus Type:
- gene with protein product
- Date approved:
- 1993-03-03
- Date modifiied:
- 2019-04-23
- Gene:
- GIHCG NIH gene
- Name:
- GIHCG inhibitor of miR-200b/200a/429 expression
- Previous symbol:
- -
- Synonyms:
- lncRNA-GIHCG
- Chromosome:
- 12q14.1
- Locus Type:
- RNA, long non-coding
- Date approved:
- 2018-07-25
- Date modifiied:
- 2019-01-25
Related products to: Mouse Monoclonal to CD105 / Endoglin, Clone MEM-229, Isotype IgG2aApplication FC, WB, IHC(F), ICC Concentration 1 mg/ml
Related articles to: Mouse Monoclonal to CD105 / Endoglin, Clone MEM-229, Isotype IgG2aApplication FC, WB, IHC(F), ICC Concentration 1 mg/ml
- Electroneurography (ENG) provides an objective tool for assessing nerve function and characterizing electrophysiological profiles. The underutilization of ENG in our setting limits the early diagnosis of peripheral neuropathy (PN), a frequent complication of type 2 diabetes. This study aimed to describe electroneurographic parameters in diabetic subjects (DS) in relation to neuropathic pain (NP) and to compare them with non-diabetic controls (NDS) in Lubumbashi, in order to identify abnormalities specifically attributable to diabetes. - Source: PubMed
Publication date: 2026/09/23
Ngoy Mande Jean-PaulBilonda Mbuyamba EuniceMusa Obadia PaulNgoy Nkulu DophraBanza Lubaba CélestinMukalay Wa Mukalay Abdon SylvestreLelubre ChristopheRis LaurenceOkitundu Luwa E-Andjafono Daniel - Lumbar spinal loads differ across various scenarios, including lumbar extension in the lateral recumbent position, seated/standing trunk extension, upright sitting or standing, muscular tension, muscular relaxation, and whole-body vibration. Nevertheless, systematic comparative studies concerning lumbar biomechanical behaviors under these diverse scenarios remain scarce. To provide guidance and references for clinical biomechanics and simulation studies, this study adopts a validated lumbar-pelvic (L3-P) finite element model to investigate the biomechanical characteristics of the lumbar spine under various loading conditions. The maximum von Mises stress in the annulus fibrosus was located at the L5-S1 intervertebral disc under moment and follower-load conditions, whereas the maximum stress occurred at the L4-L5 intervertebral disc under gravity conditions. The maximum pressure in the nucleus pulposus consistently appeared at the L3-L4 segment under all applied loads. The facet joint contact force increased toward the lower lumbar spine. The loading sequence affected the transient process rather than the final results. Under whole-body vibration, the relaxed posture led to higher lumbar spinal loads and stresses, whereas a tensed muscular state reduced such loads and stresses. Therefore, appropriate loading conditions should be selected according to lumbar spinal status in clinical practice and simulation studies to achieve accurate evaluation and analysis. - Source: PubMed
Publication date: 2026/10/08
Zhang Jing-FangZhang JiangYang Yan-AnDong Rui-ChunLi Qian - Whole-body vibration (WBV) is widely used in rehabilitation, clinical practice and sports to improve various health conditions and enhance muscle performance. However, the biomechanical mechanisms underlying these beneficial effects remain unclear. Although vibration transmission during WBV training has been investigated in standing postures, seated postures remain largely unexplored. This study investigated how three sitting postures (slouched, upright, and tense) affect vibration transmission to and through the human body during WBV exposure. Twelve healthy male participants were exposed to vertical sinusoidal vibration with amplitude of 14.3 m/s and frequency of 30 Hz while seated on a force plate mounted on the vibrating platform of a WBV training machine. Vertical and fore-and-aft head accelerations and interface forces between the body and the vibrating platform were measured. The tense posture produced significantly greater vertical and fore-and-aft head accelerations than the slouched and upright postures, indicating increased vibration transmissibility to the head with upper-body stiffening. In contrast, interface forces did not differ significantly among postures. It was concluded that sitting posture influences vibration transmission to the head during WBV exposure, whereas its effect on interface forces appears limited. A tense sitting posture increases head vibration transmissibility, emphasising the importance of posture when designing safe and effective WBV interventions. - Source: PubMed
Publication date: 2026/10/08
Nawayseh NaserHummieda AmmarZidan OmarSingh Amandeep - Fluoroscopy-guided spinal interventions require anatomically representative and radiographically compatible physical models for procedural simulation. Cadaveric specimens and animal models, while valuable, are limited by cost, availability, ethical considerations, and restricted repeatability. These limitations motivate the development of cost-efficient lumbar spine simulators compatible with C-arm fluoroscopic imaging. Vertebrae and pelvic structures were generated from open-source STL files and fabricated using fused deposition modeling. Post-processing included surface polishing and fabrication of silicone molds to reproduce vertebral geometry. Combinations of two-component polyurethane casting resin, calcium sulfate, barium sulfate, and iohexol were tested to evaluate radiographic visibility and identify a suitable radiopaque formulation. Vertebral elements were assembled using silicone interfaces to form puncturable intervertebral spaces. Soft tissues and skin were imitated using gelatin-glycerin foam and pigmented silicone. Radiographic appearance was assessed under C-arm fluoroscopy. Among the tested formulations, polyurethane composite containing 5 wt% calcium sulfate provided sufficient radiographic visibility while avoiding excessive radiopacity and was selected for the final simulator. The simulator reproduced key lumbar anatomical features and enabled clear visualization of the needle trajectory under fluoroscopy. Design optimization produced a lighter and more compact configuration than the initial prototype. This study presents a reproducible 3D-printed lumbar spine simulator with tunable radiographic properties compatible with fluoroscopic imaging. The proposed design provides a cost-efficient physical model for image-guided procedural simulation and technical development, intended for non-commercial academic and educational use. - Source: PubMed
Publication date: 2026/10/08
Ozherelev AleksandrBandur VeronikaPolkin RomanGoncharuk Roman - Sodium-based batteries are emerging as promising alternatives to lithium technologies owing to the abundance and low cost of sodium. However, their performance is strongly governed by electrolyte chemistry. This perspective examines the role of glyme-based electrolytes in sodium batteries, with particular emphasis on Na-O2 systems, where the electrolyte actively participates in electrochemical reactions. The effect of glyme chain length, sodium salt identity and salt concentration on the shape of Na⁺ solvation structures, ion pairing, mass transport, superoxide solubility and solid-electrolyte interphase formation are discussed. These interrelated effects control oxygen reduction and evolution kinetics, discharge product formation and long-term reversibility, highlighting the limitations of classical electrolyte descriptors based solely on conductivity or viscosity. The analysis shows that optimal electrolyte performance in Na-O2 batteries arises from a balance between solvation stability, transport properties and interfacial chemistry rather than from maximizing isolated bulk parameters. Comparisons with sodium-ion batteries further emphasize the broader relevance of coordination chemistry and desolvation processes. Finally, this perspective argues for a redefinition of what constitutes a 'good solvent' in reactive battery systems, integrating molecular-level solvation, interfacial reactivity, safety and sustainability considerations. Such an approach is essential for advancing efficient, durable and environmentally responsible sodium-based energy storage technologies. This article is part of the theme issue 'Electrolytes within the domain of electrochemistry and electrochemical energy storage'. - Source: PubMed
Ruiz de Larramendi IdoiaBeitia JulenGoikolea EiderPozo-Gonzalo CristinaOrtiz Vitoriano Nagore