HCYP2MAG-62K
MILLIPLEX® 人细胞因子/趋化因子磁珠板II - 免疫学多重分析
Simultaneously analyze multiple cytokine and chemokine biomarkers with Bead-Based Multiplex Assays using the Luminex technology, in human serum, plasma and cell culture samples.
别名:
Human cytokine multiplex kit, Luminex® human cytokine immunoassay, Millipore human cytokine panel
产品名称
MILLIPLEX® 人细胞因子/趋化因子磁珠板II - 免疫学多重分析, Simultaneously analyze multiple cytokine and chemokine biomarkers with Bead-Based Multiplex Assays using the Luminex technology, in human serum, plasma and cell culture samples.
species reactivity
human
manufacturer/tradename
Milliplex®
assay range
accuracy: 81-110%
sensitivity: 0.4-55.8 pg/mL
standard curve range: 1.0-100,000 pg/mL
technique(s)
multiplexing: suitable
detection method
fluorometric (Luminex xMAP)
shipped in
wet ice
Quality Level
Application
- 分析物：6Ckine, BCA-1, CTACK, ENA-78, Eotaxin-2, Eotaxin-3, I-309, IL-16, IL-20, IL-21, IL-23, IL-28A, IL-33, LIF, MCP-2, MCP-4, MIP-1δ, SCF, SDF-1A+β, TARC, TPO, TRAIL, TSLP
- 推荐的样品类型：血清，血浆和细胞培养上清液
- 推荐的样品稀释度：未稀释
- 分析运行时间：过夜或2小时初次孵育。为了获得最佳结果，建议过夜孵育
- 研究类别：炎症 & 免疫学
- 研究子类别：肥胖，代谢紊乱，炎症 & 自身免疫机制
Biochem/physiol Actions
交叉反应性
对于该面板中的任何其他分析物，抗体之间没有或有可以忽略不计的交叉反应性。
对于该面板中的任何其他分析物，抗体之间没有或有可以忽略不计的交叉反应性。
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明，否则我们的产品仅供研究使用，不得用于任何其他目的，包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
Features and Benefits
通过在此面板中选择可用的分析物来设计多重试剂盒。
General description
“细胞因子”是用于多种可溶性蛋白质和肽的通用术语，其在正常和病理条件下充当调节剂以调节单个细胞和组织的功能活性。这些蛋白质还介导细胞之间的直接各种相互作用并调节细胞外环境中发生的过程。细胞因子组蛋白包括淋巴因子、干扰素、集落刺激因子和趋化因子。细胞因子和趋化因子研究对于更深入地了解免疫系统及其对大多数抗原的多方面反应以及疾病状态（例如炎症性疾病，过敏反应，肠易激综合征（IBD），脓毒症和癌症）具有重要作用。
MILLIPLEX®人细胞因子/趋化因子面板II使您能够专注于细胞因子的治疗潜力以及细胞因子表达的调节。
Luminex® xMAP®平台使用磁珠免疫分析格式，以实现理想的速度和灵敏度，同时定量多种分析物，从而显著提高生产力，同时节省宝贵的样本量。
面板类型：细胞因子/趋化因子
MILLIPLEX®人细胞因子/趋化因子面板II使您能够专注于细胞因子的治疗潜力以及细胞因子表达的调节。
Luminex® xMAP®平台使用磁珠免疫分析格式，以实现理想的速度和灵敏度，同时定量多种分析物，从而显著提高生产力，同时节省宝贵的样本量。
面板类型：细胞因子/趋化因子
Other Notes
请联系技术服务部进行稀释度线性研究。
Packaging
96孔板
Preparation Note
试剂盒组分建议的存储温度为2-8°C。
Legal Information
Luminex is a registered trademark of Luminex Corp
MILLIPLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
xMAP is a registered trademark of Luminex Corp
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2
target_organs
Respiratory Tract
存储类别
10 - Combustible liquids
法规信息
新产品
此项目有
Fawaz Y Azizieh et al.
Journal of inflammation research, 12, 99-108 (2019-05-24)
Objective: In addition to some well-characterized bone turnover markers (BTMs), cytokines and adipokines have also been suggested to be linked to osteoporosis seen in menopause. However, there is much controversy on the possible association between these markers and bone mineral density
Cecilia K Andersson et al.
The Journal of allergy and clinical immunology, 139(6), 1819-1829 (2016-10-18)
Neutrophils and IL-17A have been linked mechanistically in models of allergic airways disease and have been associated with asthma severity. However, their role in pediatric asthma is unknown. We sought to investigate the role of neutrophils and the IL-17A pathway
Evidence of enhanced systemic inflammation in stable kidney transplant recipients with low Framingham risk scores.
Mansell, H; Rosaasen, N; Dean, J; Shoker, A
Clinical Transplantation null
Carsten U Niemann et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 22(7), 1572-1582 (2015-12-15)
Chronic lymphocytic leukemia (CLL) cells depend on microenvironmental interactions for proliferation and survival that are at least partially mediated through B-cell receptor (BCR) signaling. Ibrutinib, a Bruton tyrosine kinase inhibitor, disrupts BCR signaling and leads to the egress of tumor
Myung-Ho Kim et al.
medRxiv : the preprint server for health sciences (2021-03-25)
We analyzed the plasma levels of interferons and cytokines, and the expression of interferon-stimulated genes in peripheral blood mononuclear cells in COVID-19 patients with different disease severity. Mild patients exhibited transient type I interferon responses, while ICU patients had prolonged
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