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EasySep™人静息CD4+ T细胞分选试剂盒

免疫磁珠正选试剂盒

产品号 #(选择产品)

产品号 #17962_C

免疫磁珠正选试剂盒

产品优势

  • 操作简单、快捷,且无需分离柱
  • 纯度高达99%
  • 分选得到的细胞不带标记

产品组分包括

  • EasySep™人静息CD4+ T细胞分选试剂盒(产品号 #17962)
    • EasySep™人静息CD4+ T细胞分选抗体混合物,1 mL
    • EasySep™人CD25去除抗体混合物,1 mL
    • EasySep™ Dextran RapidSpheres™  ,1 mL
    • RoboSep™空管
  • RoboSep™人静息CD4+ T细胞分选试剂盒(产品号 #17962)
    • EasySep™人静息 CD4+ T细胞分选抗体混合物,1 mL
    • EasySep™人CD25去除抗体混合物,1 mL
    • EasySep™ Dextran RapidSpheres™ ,1 mL          
    • RoboSep™空管
    • RoboSep™ 缓冲液(产品号 #20104)
    • RoboSep™过滤枪头(产品号20125)
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总览

EasySep™ 人静息CD4+ T细胞分选试剂盒通过免疫磁珠负选,从新鲜或冻存的外周血单个核细胞或白细胞单采样本中,分选静息 CD4+ T细胞。EasySep™ 分选操作步骤包括抗体复合物和磁珠标记非目的细胞,使用 EasySep™磁极,只需将所需细胞倒入到新的试管中,即可将被磁珠标记的细胞与未被标记的目的细胞分离。    

磁体兼容性
• EasySep™ Magnet (Catalog #18000) • “The Big Easy” EasySep™ Magnet (Catalog #18001) • EasyEights™ EasySep™ Magnet (Catalog #18103) • RoboSep™-S (Catalog #21000)
 
亚型
细胞分选试剂盒
 
细胞类型
T 细胞,T 细胞,CD4+
 
种属

 
样本来源
Leukapheresis,PBMC
 
筛选方法
Negative
 
应用
细胞分选
 
品牌
EasySep,RoboSep
 
研究领域
免疫
 

实验数据

(A) Starting with fresh PBMCs, the resting CD4+ T cell content (CD3+CD4+CD8-CD25-CD69-HLA-DR-) of the isolated fraction is typically 95.5 ± 6.5% (mean ± SD using the purple EasySep™ Magnet). In the above example, the purities of the start and final isolated fractions are 35% and 99%, respectively. (B) Starting with fresh PBMCs that have elevated CD25/CD69/HLA-DR expression, the resting CD4+ T cell content of the isolated fraction is typically 88.0 ± 7.0% (mean ± SD using the purple EasySep™ Magnet). In the above example, the purities of the start and final isolated fractions are 8% and 85%, respectively.

产品说明书及文档

请在《产品说明书》中查找相关支持信息和使用说明,或浏览下方更多实验方案。

Document Type
Product Name
Catalog #
Lot #
Language
Catalog #
17962RF
Lot #
All
Language
English
Catalog #
17962
Lot #
All
Language
English
Document Type
Safety Data Sheet 1
Catalog #
17962RF
Lot #
All
Language
English
Document Type
Safety Data Sheet 2
Catalog #
17962RF
Lot #
All
Language
English
Document Type
Safety Data Sheet 3
Catalog #
17962RF
Lot #
All
Language
English
Document Type
Safety Data Sheet 4
Catalog #
17962RF
Lot #
All
Language
English
Document Type
Safety Data Sheet 1
Catalog #
17962
Lot #
All
Language
English
Document Type
Safety Data Sheet 2
Catalog #
17962
Lot #
All
Language
English
Document Type
Safety Data Sheet 3
Catalog #
17962
Lot #
All
Language
English

应用领域

本产品专为以下研究领域设计,适用于工作流程中的高亮阶段。探索这些工作流程,了解更多我们为各研究领域提供的其他配套产品。

相关材料与文献

技术资料 (8)

文献 (2)

Endothelial Cells Promote Productive HIV Infection of Resting CD4+ T Cells by an Integrin-Mediated Cell Adhesion-Dependent Mechanism. C. M. Card et al. AIDS research and human retroviruses 2022 feb

Abstract

Resting CD4+ T cells are primary targets of early HIV infection events in vivo, but do not readily support HIV replication in vitro. This barrier to infection can be overcome by exposing resting CD4+ T cells to endothelial cells (ECs). ECs line blood vessels and direct T cell trafficking into inflamed tissues. Cell trafficking pathways have been shown to have overlapping roles in facilitating HIV replication, but their relevance to EC-mediated enhancement of HIV susceptibility in resting CD4+ T cells has not previously been examined. We characterized the phenotype of primary human resting CD4+ T cells that became productively infected with HIV when cocultured with primary human blood and lymphatic ECs. The infected CD4+ T cells were primarily central memory cells enriched for high expression of the integrins LFA-1 and VLA-4. ICAM-1 and VCAM-1, the cognate ligands for LFA-1 and VLA-4, respectively, were expressed by the ECs in the coculture. Blocking LFA-1 and VLA-4 on resting CD4+ T cells inhibited infection by 65.4%-96.9%, indicating that engagement of these integrins facilitates EC-mediated enhancement of productive HIV infection in resting CD4+ T cells. The demonstration that ECs influence cellular HIV susceptibility of resting memory CD4+ T cells through cell trafficking pathways engaged during the transmigration of T cells into tissues highlights the physiological relevance of these findings for HIV acquisition and opportunities for intervention.
Hepatitis C Virus Influences HIV-1 Viral Splicing in Coinfected Patients. P. Mart\'inez-Rom\'an et al. Journal of clinical medicine 2020 jul

Abstract

Coinfection with hepatitis C virus (HCV) influences HIV reservoir size. However, it is unknown whether this coinfection also induces a higher provirus transcription. Viral transcription is promoted by synergy between cellular factors such as NF-$\kappa$B and the viral regulator Tat. The impact of HCV coinfection on HIV provirus transcription was analyzed in resting (r)CD4 T+ cells (CD3+CD4+CD25-CD69-HLADR-) and rCD4 T cells-depleted PBMCs (rCD4 T- PBMCs) from a multicenter cross-sectional study of 115 cART-treated HIV patients: 42 HIV+/HCV+ coinfected individuals (HIV+/HCV+), 34 HIV+ patients with HCV spontaneous clearance (HIV+/HCV-) and 39 HIV patients (HIV+). Viral transcription was assessed in total RNA through the quantification of unspliced, single spliced, and multiple spliced viral mRNAs by qPCR. Linear correlations between viral reservoir size and viral splicing were determined. A 3-fold increase of multiple spliced transcripts in rCD4 T+ cells of HIV+/HCV+ patients was found compared to HIV+ individuals (p {\textless} 0.05). As Tat is synthesized by multiple splicing, the levels of Tat were also quantified in these patients. Significant differences in single and multiple spliced transcripts were also observed in rCD4 T- PBMCs. Levels of multiple spliced mRNAs were increased in rCD4 T+ cells isolated from HIV+/HCV+ subjects, which could indicate a higher Tat activity in these cells despite their resting state.

更多信息

更多信息
种属 Human
Magnet Compatibility • EasySep™ Magnet (Catalog #18000) • “The Big Easy” EasySep™ Magnet (Catalog #18001) • EasyEights™ EasySep™ Magnet (Catalog #18103) • RoboSep™-S (Catalog #21000)
样本来源 Leukapheresis, PBMC
Selection Method Negative
质量保证:

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