CD43
- Known as:
- CD43
- Catalog number:
- 10-220-C100
- Product Quantity:
- 0.1 mg
- Category:
- -
- Supplier:
- Exbio
- Gene target:
- CD43
Ask about this productRelated genes to: CD43
- Gene:
- SPN NIH gene
- Name:
- sialophorin
- Previous symbol:
- -
- Synonyms:
- LSN, CD43, GPL115
- Chromosome:
- 16p11.2
- Locus Type:
- gene with protein product
- Date approved:
- 1988-08-31
- Date modifiied:
- 2016-07-19
Related products to: CD43
Related articles to: CD43
- Lithium-sulfur (Li-S) batteries are promising next-generation energy storage systems, yet critical challenges including severe sulfur volume expansion, uncontrolled lithium polysulfide (LiPS) shuttling, and sluggish sulfur redox kinetics impede their practical application. Herein, we develop a metal-organic framework (MOF) functionalization strategy across three distinct structural modules (MOF backbone, grafted modulators, and engineered pore space) to tackle these issues. Specifically, in the newly synthesized Zr-based topology FDM-221, its high surface area (1956 m g) and large pore volume (1.35 cm g) provide ample pore space to accommodate sulfur volume expansion even after high sulfur encapsulation. Furthermore, sulfiphilic sites (coordinatively unsaturated Zr(IV) in the framework backbone) and lithiophilic moieties (S atoms from the benzotrithiophene-based linker and F atoms from the dangling modulators) work in tandem to furnish robust binding sites for LiPS adsorption while concurrently accelerating the redox catalysis of sulfur species. Li-S batteries based on this trinity structure deliver a high capacity of 1164 mAh g at 0.1C and excellent cycling stability over 1000 cycles at 2C, demonstrating the great potential of this MOF design strategy for next-generation batteries. - Source: PubMed
Publication date: 2026/06/25
Sun YuqianWang BohanLi WangzhiJiang ZhongwenLi TongXi HaozhiYan YuLi Qiaowei - Although relatively rare, pediatric pancreatic tumors have been increasingly reported in the literature. Our aim was to systematically review the literature on the clinical characteristics, management, and outcomes of pediatric pancreatic tumors. - Source: PubMed
Publication date: 2026/06/23
Kakos Christos DZiogas Ioannis AKokkinakis StamatiosKhomiak AndriiMoris DimitriosMarantos AngelosDionysis Theodoros TSchulick Richard DDel Chiaro MarcoRoach Jonathan P - The optimal surgical strategy for early-stage lung adenocarcinoma appearing as part-solid nodules (PSN) versus pure solid nodules (SPN) remains debated. This study directly compares their clinicopathological features, surgical outcomes, and recurrence patterns to inform personalized management based on CT characteristics. - Source: PubMed
Li HanyueYu RunhuaGuo SongyuanWang YiyangGu ZhitaoFang Wentao - Sympathetic preganglionic neurons (SPNs) provide the sole spinal output to the peripheral sympathetic nervous system. Although sympathetic control is traditionally attributed to synaptic integration within the spinal cord and ganglia, the reliability of spike propagation along SPN axons themselves has received little attention. Here, and in companion papers, we show that axonal conduction in adult mouse thoracic SPNs is highly modifiable and constitutes a critical site of sympathetic gain control. Using an preparation preserving intact paravertebral and splanchnic pathways while blocking synaptic transmission, we recorded compound action potentials evoked across multiple ganglia. Slower-conducting, unmyelinated SPN axons, particularly those with branching axons traversing the interganglionic nerve (IGN), exhibited pronounced, temperature-dependent conduction failures. Elevation of temperature produced membrane hyperpolarization and loss of conduction, consistent with activation of temperature-sensitive K P leak channels, as supported by pharmacological evidence. Pharmacological activation of TREK-family channels with riluzole or arachidonic acid preferentially suppressed conduction in these axons. In contrast, blockade of voltage-gated K channels with 4-aminopyridine (4-AP) robustly facilitated conduction, recruited previously silent axons, and restored propagation under conditions of temperature-induced failure. Surprisingly, tetraethylammonium (TEA) block of K channels were without effect or depressant. Transmitter systems further shaped axonal reliability: agonists and antagonists of GABA receptors, as well as cholinergic manipulations, selectively depressed conduction in slow, branching axons. Together, these findings establish SPN axons, particularly slow-conducting branching fibers, as an active and dynamically regulated substrate for sympathetic output control, revealing a presynaptic mechanism with implications for autonomic physiology and disease. - Source: PubMed
Publication date: 2026/06/08
Halder MallikaHochman Shawn - Domestication and conservation research often relies on single-species frameworks, which can obscure how Indigenous management practices applied to multiple related taxa may interact to shape shared gene pools. Studies of crops such as manioc/cassava (Manihot esculenta), yam (Dioscorea spp.), sorghum (Sorghum spp.), and Amazonian treegourd (Crescentia spp.) demonstrate that domestication frequently involves interactions among multiple cultivated and wild or semi-managed relatives. However, little is known about how these dynamics operate within the genus Xanthosoma, particularly in the Ecuadorian upper Amazon, a key center of diversity and domestication history for the genus. This gap limits understanding of how Indigenous management practices may influence the maintenance, erosion, or redirection of genetic diversity, with implications for crop improvement, resilience under changing environmental conditions, and the identification of underutilized plant resources. - Source: PubMed
Publication date: 2026/06/21
White John RobertZarrillo SoniaAltamirano Álvaro MonterosCevallos Marcia PeñafielTanguila RoxanaCuéllar Andrea M