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CellTraceTM CFSE Cell Proliferation Kit, for flow cytometry

CellTrace TM CFSE细胞增殖试剂盒,用于流式细胞术

公司名称: Thermo Fisher Scientific
产品编号: C34554
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In vivo Priming of T Cells with in vitro Pulsed Dendritic Cells: Popliteal Lymph Node Assay
Author:
Date:
2017-09-05
[Abstract]  One-way mixed lymphocyte reaction (MLR) is a classic tool to measure how T cells react to external stimuli. However, MLR is an in vitro reaction system, which shows different response intensity compared with in vivo trails sometimes due to the lack of cytokines, tissue matrix and other immune response associated factors. The following popliteal lymph node assay (PLNA) protocol is designed to test the T cells antigen-specific reaction in vivo by using ovalbumin (OVA) specific reacted transgenic mouse OT-1 and OT-2. [摘要]  单向混合淋巴细胞反应(MLR)是测量T细胞如何与外部刺激反应的经典工具。 然而,MLR是体外反应系统,其与体内踪迹相比显示出不同的反应强度,有时由于缺乏细胞因子,组织基质和其他免疫应答相关因素。 设计了以下po淋巴结测定(PLNA)方案,通过使用卵白蛋白(OVA)特异性反应的转基因小鼠OT-1和OT-2,体内测试T细胞抗原特异性反应。
【背景】在移植中,自身免疫和感染研究中,单向混合淋巴细胞反应(MLR)是评估T细胞增殖在抗原存在细胞(APC)或其他外部刺激反应中是否增加或抑制的有用参数。 这是一个典型的功能测试,它展示了T细胞如何受到免疫抑制药物(Hou et al。,2015; Zhang et al。,2015),阴性细胞或外来体疫苗(Ma)的测试试剂的影响 et al。,2016; Cai et al。,2017)。
   然而,由于体外免疫反应系统,该系统具有一定的限制。 体内免疫反应受生物微环境的影响,如细胞因子,趋化因子,激素分泌,组织基质等未知生物因子。
   在这里,po淋巴结测定(PLNA)被设计为体内工具,通过使用卵白蛋白(OVA)抗原特异性反应系统来测试增加或减少的免疫应答(Bhatt等,2014; Cai et al。,2017)。

Evaluation of Cross-presentation in Bone Marrow-derived Dendritic Cells in vitro and Splenic Dendritic Cells ex vivo Using Antigen-coated Beads
Author:
Date:
2016-11-20
[Abstract]  Antigen presentation by MHC class I molecules, also referred to as cross-presentation, elicits cytotoxic immune responses. In particular, dendritic cells (DC) are the most proficient cross-presenting cells, since they have developed unique means to control phagocytic and degradative pathways.

This protocol allows the evaluation of antigen cross-presentation both in vitro (by using bone marrow-derived DC) and ex vivo (by purifying CD8+ DC from spleen after incorporation of particulate antigen) using ovalbumin (OVA)-coupled particles. Cross-presentation ...
[摘要]  通过MHC I类分子的抗原呈递,也称为交叉呈递,引起细胞毒性免疫应答。特别地,树突细胞(DC)是最熟练的交叉呈递细胞,因为它们已经开发了控制吞噬和降解途径的独特手段。 <此协议允许在体外(通过使用骨髓衍生的DC)和离体(通过纯化CD8 + )评价抗原交叉呈递。 (OVA)偶联的颗粒后,来自脾脏的DC/DC结合颗粒抗原)。通过三种不同的读数测量交叉呈递效率:B3Z杂交瘤T细胞系(Karttunen等人,1992)和抗原特异性CD8 + T细胞的刺激OT-I)(Kurts等人,1996),在用羧基荧光素琥珀酰亚胺酯(CFSE)标记它们之后分析CD69表达或OT-I增殖的OT-I活化。通过使用这种方法,我们可以最近显示DCs能够在TLR4结合时瞬时增加交叉表达效率(Alloatti等人,2015)。 [背景] 在小鼠中,抗原呈递细胞(APC)能够吸收外源抗原以加工它们,并将源自这些外源抗原的肽加载到主要组织相容性复合体(MHC)I类分子上。肽-MHC I复合物随后被转运到质膜,在那里它们可以呈递到CD8 + T细胞,从而促进T细胞活化,这被称为交叉呈递(Joffre等人, al 。,2012)。在不同的APC中,树突状细胞(DC)在交叉呈递方面表现优异,并且包含表达XCR1标记的不同亚群,其已经显示非常有效地交叉呈递抗原(即CD8 + 来自脾的DC和来自皮肤和肺的CD103 ...

Lung Clearance Assay
Author:
Date:
2013-03-05
[Abstract]  Lung clearance assay tests the ability of innate immune cells (mainly NK cells) to eradicate in vivo cells injected via the tail vein of the mice. This assay helps to elucidate the role played by NK cells and their receptors (if the mice are genetically modified) against various human and mouse targets in an in vivo setting (Stern-Ginossar et al., 2008; Halfteck et al., 2009; Tsukerman et al., 2012).
[摘要]  该实验方案的中文版正在准备中...

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