GMCSF
- Known as:
- GMCSF
- Catalog number:
- ANT-129
- Product Quantity:
- 500µg
- Category:
- -
- Supplier:
- Prospecbio
- Gene target:
- GMCSF
Related genes to: GMCSF
- Gene:
- CSF2 NIH gene
- Name:
- colony stimulating factor 2
- Previous symbol:
- -
- Synonyms:
- GM-CSF, GMCSF
- Chromosome:
- 5q31.1
- Locus Type:
- gene with protein product
- Date approved:
- 2001-06-22
- Date modifiied:
- 2018-12-12
Related products to: GMCSF
Anserine Colony Stimulating Factor 2, Granulocyte Macrophage Elisa Kit (GMCSF)Anserine anti - Colony Stimulating Factor 2, Granulocyte Macrophage Elisa Kit (GMCSF)Antigens GM-CSF, 18-141 aa, Mouse, Recombinant, E.coliAntiHuman GMCSF (F43) PurifiedBovine anti-Colony Stimulating Factor 2, Granulocyte Macrophage Elisa Kit (GMCSF)Bovine Colony Stimulating Factor 2, Granulocyte Macrophage Elisa Kit (GMCSF)Canine Colony Stimulating Factor 2, Granulocyte Macrophage (GMCSF) ELISA KitCanine Colony Stimulating Factor 2, Granulocyte Macrophage Elisa Kit (GMCSF)Canine Colony Stimulating Factor 2, Granulocyte Macrophage(GMCSF)ELISA KitCanine Colony Stimulating Factor 2, Granulocyte Macrophage(GMCSF)ELISA KitCanine Colony Stimulating Factor 2, Granulocyte Macrophage(GMCSF)ELISA KitCanine Colony Stimulating Factor 2, Granulocyte Macrophage,GMCSF ELISA KitCanine GCSF protein GMCSF k9 Recombinant produced in E.coli is a single, non-glycosylated, polypeptide chain containing 128 amino acids and having a molecular mass of 14.2 kDa. GM-CSF is purified by pCanine GMCSF ELISA KitChicken GMCSF/CSF2(Granulocyte Macrophage Colony Stimulating Factor 2) ELISA Kit Related articles to: GMCSF
- Air pollution has been associated with the development and exacerbation of atopic dermatitis (AD), but the molecular signatures connecting pollutant-related targets with AD-associated immune dysregulation remain incompletely characterized. - Source: PubMed
Publication date: 2026/09/03
Gao ChangChen LipingHuang TianfengWang Zi - Skin wound healing remains a prominent clinical challenge, creating an urgent demand for high-performance wound-care biomaterials. Deaminotyrosine (DAT), a recently identified flavonoid-derived gut metabolite, exhibits anti-inflammatory and immunomodulatory activities. Nevertheless, its translational application is greatly restricted by poor aqueous solubility, insufficient stability, and potential dose-dependent toxicity. Herein, we fabricated a novel zirconium-based metal-organic framework carrier loaded with DAT (denoted DAT@Zr-MOF). The resulting nanocomposite displayed a uniform spherical morphology, favorable colloidal stability, and satisfactory drug loading capacity. experiments verified its desirable hemocompatibility and cytocompatibility. DAT@Zr-MOF could be efficiently internalized by HUVECs and markedly facilitate endothelial angiogenesis, proliferation, and migration. Additionally, it inhibited LPS-triggered NF-κB signaling activation, TNF-α secretion, and ROS accumulation in RAW264.7 macrophages. After integration into a thermosensitive poloxamer 407 hydrogel, DAT@Zr-MOF significantly accelerated wound closure in a murine full-thickness skin defect model. The formulation facilitated re-epithelialization, collagen deposition, and neovascularization, achieving superior therapeutic effects relative to the blank control and free DAT groups. RNA-seq profiling of day-15 wound tissues identified 549 differentially expressed genes (DEGs). Functional enrichment analyses indicated that these DEGs were closely associated with core biological events, including skin development, keratinocyte differentiation, cytokine-receptor interactions, and leukocyte migration. Protein-protein interaction network analysis further uncovered hub genes such as , , and . Collectively, the DAT@Zr-MOF composite hydrogel expedites cutaneous wound healing by synergistically modulating angiogenesis, inflammatory response and tissue remodeling through multi-pathway transcriptional regulation. This study offers a promising strategy for the design of advanced wound dressings. - Source: PubMed
Publication date: 2026/09/14
Li Zheng-YuanYang JinPeng Xiao-YunMeng Pan-PanChen LinCao TanChang Bei-LeiWang YueHu Yue-YaoLi Tong-FeiLi Xian-YuDing Yan - BackgroundSystemic inflammation has been implicated in cognitive aging and neurodegeneration; however, inflammatory biomarkers are expressed in coordinated patterns rather than as isolated markers.ObjectiveTo identify latent inflammatory biomarker groupings and evaluate their associations with cognitive performance among midlife and older adults.MethodsThis cross-sectional study included 334 participants from the Aging Research Characterizing Health Exposome via Social Drivers (ARCHES) study. Cognitive performance was assessed using the Preclinical Alzheimer Cognitive Composite (PACC). Plasma inflammatory biomarkers were quantified using the NuLISA™ multiplex immunoassay platform. Exploratory factor analysis (EFA) (minimum residual extraction, oblimin rotation) identified latent inflammatory factors, retaining biomarkers with loadings ≥0.40. Factor scores were evaluated in multivariable linear regression models adjusted for age, sex, education, and genotype status; sensitivity analyses adjusted for socioeconomic context, medication use, BMI, lifestyle factors, and clinical diagnoses. Age-stratified and nonlinear spline analyses were conducted.Results27 of 43 biomarkers formed an eight-factor structure explaining 43% of variance. Two factors were significantly associated with cognitive performance after FDR correction. Factor 4 (CCL4, CXCL1, S100A12) and Factor 5 (IL2, IL5, IL13, IL10, CSF2) were inversely associated with PACC scores. These associations remained consistent across sensitivity analyses. Age-stratified analyses showed that several inflammatory factors were associated with cognitive performance among participants aged 45-<65 years, whereas no factors remained significant among participants aged ≥65 years after FDR correction. Nonlinear modeling indicated a non-linear age-cognitive performance relationship.ConclusionsEFA identified clusters of correlated inflammatory biomarkers associated with cognitive performance in this cohort of midlife and older adults. - Source: PubMed
Publication date: 2026/09/02
Singh Ramkrishna KBekena SemereWalker Alexis I BTaylor KaylinZhu YiqiPal SubrataMohamed Essa ATrani Jean-FrancoisKaplan IanBabulal Ganesh M - IL-17-producing Type 17 T (T17) cells are central drivers of inflammation in both psoriasis and hidradenitis suppurativa (HS), as evidenced by the clinical efficacy of IL-17-targeting therapies. However, therapeutic responses differ substantially between diseases, raising the possibility that the composition and regulation of T17 states are disease context dependent. - Source: PubMed
Publication date: 2026/08/14
Park NayoungLee JongeunKim DayeonRambhia DarshnaKim JaebumZhou WeiCao JunyueKrueger James GKo YounheeKim Jaehwan - Chronic exposure to endocrine-disrupting chemicals has been increasingly recognized as a potential contributor to cancer progression. Monobutyl phthalate (MBP), a major metabolite of dibutyl phthalate, is widely detected in human biological samples, yet its long-term impact on anaplastic thyroid cancer (ATC) has not been systematically investigated. CAL-62 cells were continuously exposed to an environmentally relevant concentration of MBP (10 nM) over 3 months to establish a chronic exposure model that mimics long-term environmental exposure. Transcriptomic profiling was integrated with network toxicology to identify key molecular pathways and hub genes, followed by molecular docking and Western blot validation. Chronic MBP exposure significantly enhanced cell viability, proliferation, colony formation, and tumorsphere formation, indicating promotion of malignant phenotypes. Transcriptomic profiling revealed extensive molecular remodeling characterized by activation of inflammation-associated pathways, including cytokine-cytokine receptor interaction, IL-17, TNF, and JAK-STAT signaling, accompanied by suppression of p53- and mTOR-related pathways. Integrated analysis identified 57 overlapping KEGG pathways, with IL6 and CSF2 emerging as central hub genes. Molecular docking demonstrated favorable binding affinities between MBP and representative target proteins, including IL6, TP53, CASP3, BCL2, and PPARG. Western blot analysis further confirmed increased IL6 and BCL2 expression together with decreased TP53, CASP3, and PPARG expression following chronic MBP exposure. Chronic environmentally relevant MBP exposure promotes ATC malignant progression through coordinated inflammation-associated molecular network remodeling accompanied by suppression of apoptosis-related signaling. Integrating network toxicology with transcriptomic profiling provides an effective systems-level strategy for identifying biologically relevant molecular networks underlying chronic environmental toxicant exposure. - Source: PubMed
Publication date: 2026/08/04
Deng YuTan SongweiWei JinlanGuo XingyueHu LongqingQu XincaiZhou Jing