Rabbit Interleukin 6,IL-6 ELISA Kit
- Known as:
- Rabbit Interleukin 6,Interleukin-6 Enzyme-linked immunosorbent assay test Kit
- Catalog number:
- E0002Rb
- Product Quantity:
- 48T
- Category:
- Elisa Kits
- Supplier:
- JING
- Gene target:
- Rabbit Interleukin 6 IL-6 ELISA Kit
Related genes to: Rabbit Interleukin 6,IL-6 ELISA Kit
- Gene:
- CEBPB NIH gene
- Name:
- CCAAT enhancer binding protein beta
- Previous symbol:
- TCF5
- Synonyms:
- LAP, CRP2, NFIL6, IL6DBP, C/EBP-beta
- Chromosome:
- 20q13.13
- Locus Type:
- gene with protein product
- Date approved:
- 1991-02-27
- Date modifiied:
- 2018-02-23
- Gene:
- CEBPD NIH gene
- Name:
- CCAAT enhancer binding protein delta
- Previous symbol:
- -
- Synonyms:
- CRP3, CELF, C/EBP-delta, NF-IL6-beta
- Chromosome:
- 8q11.21
- Locus Type:
- gene with protein product
- Date approved:
- 1992-06-24
- Date modifiied:
- 2018-02-23
- Gene:
- ENTPD6 NIH gene
- Name:
- ectonucleoside triphosphate diphosphohydrolase 6
- Previous symbol:
- CD39L2, IL6ST2
- Synonyms:
- NTPDase-6, dJ738P15.3
- Chromosome:
- 20p11.21
- Locus Type:
- gene with protein product
- Date approved:
- 1998-03-20
- Date modifiied:
- 2019-02-28
- Gene:
- IL6 NIH gene
- Name:
- interleukin 6
- Previous symbol:
- IFNB2
- Synonyms:
- IL-6, BSF2, HGF, HSF
- Chromosome:
- 7p15.3
- Locus Type:
- gene with protein product
- Date approved:
- 1986-01-01
- Date modifiied:
- 2017-07-12
- Gene:
- IL6RP1 NIH gene
- Name:
- interleukin 6 receptor pseudogene 1
- Previous symbol:
- IL6RL1
- Synonyms:
- -
- Chromosome:
- 9q22.2
- Locus Type:
- pseudogene
- Date approved:
- 1991-08-18
- Date modifiied:
- 2014-11-19
Related products to: Rabbit Interleukin 6,IL-6 ELISA Kit
Related articles to: Rabbit Interleukin 6,IL-6 ELISA Kit
- Ocular fungal infections, represent a significant global health burden, particularly in tropical and subtropical regions. Conventional antifungal therapies often suffer from poor ocular bioavailability, delayed diagnosis, toxicity, and limited efficacy, especially in immunocompromised individuals. Given the critical role of host immunity in determining disease outcomes, immunomodulation has emerged as a promising adjunctive strategy to enhance antifungal defense while mitigating immunopathology. This review highlights the complex interplay between innate and adaptive immune responses in ocular fungal infections and explores emerging immunotherapeutic approaches such as host defense peptides, cytokine therapies (e.g., IFN-γ, IL-6, IL-17, IL-33), cellular therapies (e.g., MSCs, CAR-T cells, dendritic cells), and extracellular vesicle-based interventions. Despite existing challenges including the complexity of ocular immunopathology and the logistical hurdles of clinical trials Immunomodulatory therapies have the potential to shift the current treatment paradigm for ocular fungal infections, advancing from traditional pathogen-targeted approaches to more precise, host-directed interventions. - Source: PubMed
Publication date: 2026/05/03
Khapuinamai AgimanailiuJoseph Joveeta - This study aimed to explore the prognostic and immune-related associations of adiponectin-related genes in melanoma. - Source: PubMed
Publication date: 2026/05/03
Yin YongRen Chun - Metal additive manufacturing (AM) relies on alloy feedstock powders that may come into contact with the workers' skin during handling, yet skin-relevant data on metal release and biological reactivity remain limited. Here, we assessed the cutaneous bioactivity of the fine particle fraction of four gas-atomized Fe-based AM powders (316L stainless steel, Fe-powder A, and tooling steels B and C). Powders were sieved to <10 μm and characterized by scanning electron microscopy and X-ray photoelectron spectroscopy before and after incubation in artificial sweat (ASW). Metal biodissolution was quantified in ASW and keratinocyte culture medium using atomic absorption spectrophotometry. Cellular responses were evaluated in HaCaT keratinocytes using Cell Painting-based phenomics and multiplex cytokine/chemokine profiling and in an full-thickness human skin explant model, including superficial barrier disruption, IL-8/CXCL8 quantification, and histological assessment. ASW exposure induced marked shifts in the outermost surface composition across powders, indicating sweat-driven surface transformation. Biodissolution was low and medium-dependent, with Fe dominating the release in ASW, and with an overall metal release remaining limited in cell culture medium. In HaCaT cells, MCP-1/CCL2, IL-6, and IL-8/CXCL8 were quantifiable but showed no significant changes following powder exposure. Cell Painting revealed subtle, shared phenotypic signatures, primarily involving mitochondrial-associated features, without evidence of broad cellular stress. In the skin model, AM powders did not increase IL-8/CXCL8 secretion, the particles remained localized to the skin surface without detectable penetration, and coexposure with did not enhance bacterial colonization or induce inflammation. To the best of our knowledge, this is the first study that applies a human skin explant model to evaluate dermal responses to metal AM powders. Overall, the tested AM powders showed low short-term cutaneous reactivity under skin-relevant conditions, providing human-relevant evidence to inform occupational risk assessment in AM environments. - Source: PubMed
Publication date: 2026/05/03
Persson AlexanderŁyczyńska ZuzannaShahata MariamKotlyar OleksandrEngwall MagnusSärndahl EvaEhrström MarcusMelican KeiraOdnevall IngerAlijagic Andi - Although roles of CD44 in the genetic predisposition for bronchopulmonary dysplasia (BPD) has been recognized, the immune characteristics of CD44+ monocytes in BPD are unclear. We aimed to (1) compare the expression and function of CD44 on monocytes in BPD and non-BPD infants; (2) explore the roles of CD44 on monocytes in hyperoxia-induced inflammation. - Source: PubMed
Publication date: 2026/05/02
He YiZhou YingzhiLiu QingqingWang Nianrong - Non-small cell lung cancer (NSCLC) remains one of the leading causes of cancer-related mortality worldwide. However, the diagnostic sensitivity and specificity of commonly used tumor markers, such as carcinoembryonic antigen (CEA) and cytokeratin-19 fragment (CYFRA21-1), remain limited. This study aimed to evaluate the diagnostic value of serum exosomal 3'tiRNA-PheGAA and interleukin-6 (IL-6), alone and in combination with conventional tumor markers, for the detection of NSCLC. - Source: PubMed
Publication date: 2026/05/02
Yuan NingZhang QunShi JingCheng WenJunZhao BinZhang Zhijun