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HCP2MAG-62K-PX23

Millipore

MILLIPLEX® 人细胞因子/趋化因子磁珠板II - 预混23 Plex - 免疫学多重分析

Simultaneously analyze multiple cytokine and chemokine biomarkers with Bead-Based Multiplex Assays using the Luminex technology, in mouse serum, plasma and cell culture samples.

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About This Item

分類程式碼代碼:
12161503
eCl@ss:
32161000
NACRES:
NA.47
暫時無法取得訂價和供貨情況

品質等級

物種活性

human

製造商/商標名

Milliplex®

assay range

accuracy: 81-110%
sensitivity: 0.4-55.8 pg/mL
standard curve range: 1.0-100,000 pg/mL

技術

multiplexing: suitable

相容性

configured for Premixed

檢測方法

fluorometric (Luminex xMAP)

運輸包裝

wet ice

一般說明

“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

特異性

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。

應用

  • 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
  • 推荐的样本稀释度: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

包裝

96孔板

儲存和穩定性

试剂盒组分建议的存储温度为2-8°C。

其他說明

请联系技术服务部进行稀释度线性研究。

法律資訊

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

免責聲明

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。

訊號詞

Danger

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2

標靶器官

Respiratory Tract

儲存類別代碼

10 - Combustible liquids


分析證明 (COA)

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Sarah M Engle et al.
Clinical and experimental immunology (2022-01-13)
The pathogenesis of atopic dermatitis (AD) results from complex interactions between environmental factors, barrier defects, and immune dysregulation resulting in systemic inflammation. Therefore, we sought to characterize circulating inflammatory profiles in pediatric AD patients and identify potential signaling nodes which
Holly Mansell et al.
American journal of nephrology, 41(2), 147-155 (2015-04-01)
The 7-year Major Adverse Cardiovascular Events Calculator (CRCRTR-MACE) predicts cardiovascular events (CVE) in renal transplant recipients (RTR), and thrombopoietin (TPO) is a humoral inflammatory factor implicated in cardiovascular disease (CVD). The aim of the study was to determine if circulating
Susan Louise Lindsay et al.
Stem cell reports, 6(5), 729-742 (2016-04-28)
Previously we reported that nestin-positive human mesenchymal stromal cells (MSCs) derived from the olfactory mucosa (OM) enhanced CNS myelination in vitro to a greater extent than bone-marrow-derived MSCs (BM-MSCs). miRNA-based fingerprinting revealed the two MSCs were 64% homologous, with 26 miRNAs
Gerald V Denis et al.
PloS one, 13(5), e0196755-e0196755 (2018-05-09)
Obesity-driven Type 2 diabetes (T2D) is a systemic inflammatory condition associated with cardiovascular disease. However, plasma cytokines and tissue inflammation that discriminate T2D risk in African American women with obese phenotypes are not well understood. We analyzed 64 circulating cytokines
Mohamed El Behi et al.
Brain : a journal of neurology, 140(4), 967-980 (2017-03-24)
One major challenge in multiple sclerosis is to understand the cellular and molecular mechanisms leading to disease severity progression. The recently demonstrated correlation between disease severity and remyelination emphasizes the importance of identifying factors leading to a favourable outcome. Why

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