EasySep™小鼠ILC2富集试剂盒

免疫阴性选择试剂盒

产品号 #(选择产品)

产品号 #19842_C

免疫阴性选择试剂盒

产品优势

  • 快速,易于使用和无列
  • 分离的细胞不受影响
  • 促进ILC2s的快速流动分选

产品组分包括

  • EasySep™小鼠ILC2富集试剂盒(目录#19842)
    • EasySep™小鼠浓缩鸡尾酒,0.5 mL
    • EasySep™Streptavidin RapidSpheres™50001,1.0 mL
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概述

本产品旨在通过负选择从肺组织或其他组织的单细胞悬液中富集ILC2(2组先天淋巴样细胞)。利用生物素化抗体靶向非ilc2细胞和链亲和素包被磁颗粒(RapidSpheres™)去除不需要的细胞。使用EasySep™磁铁分离标记细胞,不使用色谱柱。

Magnet Compatibility

EasySep™ Magnet (Catalog #18000)
 
Subtype
Cell Isolation Kits
 
Cell Type
Innate Lymphoid Cells
 
Species
Mouse
 
Sample Source
Other
 
Selection Method
Negative
 
Application
Cell Isolation
 
Brand
EasySep
 
Area of Interest
Immunology
 

Data Figures

Starting with a naïve mouse lung single-cell suspension, the ILC2 content (CD45+Lin-CD278+CD90.2+ST2+) of the final enriched fraction typically ranges from 2.2 - 7.1%. In the above example, the percentage of ILC2s in the start and final enriched fractions are 0.8% and 6.5% (or 0.9% and 22.3% of CD45+ cells), respectively. NOTE: The ILC2 content of the start fraction typically ranges from 0.1 - 1%.

Protocols and Documentation

Find supporting information and directions for use in the Product Information Sheet or explore additional protocols below.

Document Type
Product Name
Catalog #
Lot #
Language
Catalog #
19842
Lot #
All
Language
English
Document Type
Safety Data Sheet 1
Catalog #
19842
Lot #
All
Language
English
Document Type
Safety Data Sheet 2
Catalog #
19842
Lot #
All
Language
English
Document Type
Safety Data Sheet 3
Catalog #
19842
Lot #
All
Language
English

Applications

This product is designed for use in the following research area(s) as part of the highlighted workflow stage(s). Explore these workflows to learn more about the other products we offer to support each research area.

Resources and Publications

Publications (2)

Isolation and adoptive transfer of innate lymphoid cells 2 to a recipient mouse model of PDAC. A. Alam et al. STAR protocols 2022 sep

Abstract

Innate lymphoid cells 2 (ILC2) play a significant role in the tumorigenesis of pancreatic ductal adenocarcinoma (PDAC). An important aspect of ILC2-mediated tumorigenesis is the expansion of the resident ILC2 and simultaneous recruitment of the peripheral ILC2. Here, we describe a protocol for isolation, enrichment, and DiD labeling of ILC2 for in vivo tracking of ILC2s in the mouse. Further, we describe steps for the adoptive transfer of ILC2 to a recipient mouse model of PDAC. For complete details on the use and execution of this protocol, please refer to Alam et al. (2022).
IL-33 induces NF-$\kappa$B activation in ILC2 that can be suppressed by in vivo and ex vivo 17$\beta$-estradiol. S. Trivedi et al. Frontiers in allergy 2022

Abstract

Asthmatic women tend to develop severe airway disease in their reproductive years, and 30%-40% of asthmatic women have peri-menstrual worsening of asthma symptoms. This indicates that fluctuations in ovarian hormones are involved in advancement of asthmatic disease and exacerbation of symptoms. Group 2 innate lymphoid cells, or ILC2, are readily detected in allergic conditions, such as rhinosinusitis, in individuals that develop nasal polyps do to allergen exposures, and in allergic asthma. ILC2 are airway localized immune cells activated by IL-33, an innate cytokine that perpetuates allergic inflammation by driving the production of IL-5 and IL-13. We have previously shown that ILC2 are highly activated in na{\{i}}ve and ovalbumin (OVA) challenged female BALB/c mice in comparison to male mice following stimulation with IL-33. Here we investigated the effect of steady-state ovarian hormones on ILC2 and the NF-$\kappa$B signaling pathway following OVA sensitization and challenge. We found that estrogen-treated ovariectomized mice (OVX-E2) that had been challenged with OVA had reduced IL-5 and IL-13 production by lung ILC2 as compared to lung ILC2 isolated from intact male and female sham-operated controls that had been treated with OVA. ILC2 were isolated from untreated animals and co-cultured ex vivo with and without estrogen plus IL-33. Those estrogen-treated ILC2 similarly produced less IL-5 and IL-13 in comparison to untreated and had reduced NF-$\kappa$B activation. Single-cell RNA sequencing showed that 120 genes were differentially expressed in male and female ILC2 and Nfkb1 was found among top-ranked regulatory interactions. Together these results provide new insight into the suppressive effect of estrogen on ILC2 which may be protective in female asthmatics. Understanding further how estrogen modulates ILC2 may provide therapeutic targets for the treatment of allergic diseases."

更多信息

更多信息
Species Mouse
Magnet Compatibility EasySep™ Magnet (Catalog #18000)
Sample Source Other
Selection Method Negative
标记抗体
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