Name: IL-22 Secretion Assay – Cell Enrichment and Detection Kit (PE), human
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Specifications

Product data and images for IL-22 Secretion Assay – Cell Enrichment and Detection Kit (PE), human

Figures

Figure 1

PBMCs were stimulated with PMA and Ionomycin or left untreated. Cells were stained according to secretion of IL-22 using the IL-22 Secretion Assay - Cell Enrichment and Detection Kit (PE), human. Displayed is the analysis of secreted IL-22 (PE) versus CD154-APC of viable CD4

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T cells (gated on CD4-FITC). B cells, monocytes, and dead cells were excluded according to CD20-PerCP, CD14-PerCP, and PI-staining respectively.

Stimulated sample

Before enrichment	After enrichment
View details IL-22 Secretion Assay – Cell Enrichment and Detection Kit (PE), human Figure 1 PBMCs were stimulated with PMA and Ionomycin or left untreated. Cells were stained according to secretion of IL-22 using the IL-22 Secretion Assay - Cell Enrichment and Detection Kit (PE), human. Displayed is the analysis of secreted IL-22 (PE) versus CD154-APC of viable CD4 ⁺ T cells (gated on CD4-FITC). B cells, monocytes, and dead cells were excluded according to CD20-PerCP, CD14-PerCP, and PI-staining respectively.	View details IL-22 Secretion Assay – Cell Enrichment and Detection Kit (PE), human Figure 1 PBMCs were stimulated with PMA and Ionomycin or left untreated. Cells were stained according to secretion of IL-22 using the IL-22 Secretion Assay - Cell Enrichment and Detection Kit (PE), human. Displayed is the analysis of secreted IL-22 (PE) versus CD154-APC of viable CD4 ⁺ T cells (gated on CD4-FITC). B cells, monocytes, and dead cells were excluded according to CD20-PerCP, CD14-PerCP, and PI-staining respectively.
Unstimulated control

Before enrichment

After enrichment

Figure 1

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T cells (gated on CD4-FITC). B cells, monocytes, and dead cells were excluded according to CD20-PerCP, CD14-PerCP, and PI-staining respectively.

Figure 1

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T cells (gated on CD4-FITC). B cells, monocytes, and dead cells were excluded according to CD20-PerCP, CD14-PerCP, and PI-staining respectively.

Specifications for IL-22 Secretion Assay – Cell Enrichment and Detection Kit (PE), human

Overview

The IL-22 Secretion Assay - Cell Enrichment and Detection Kit was developed for enrichment and sensitive detection of viable human IL-22-secreting cells.

Detailed product information

Background information

IL-22 producing cells, such as certain subtypes of T cells, dendritic cells (DCs), NK cells and other innate lymphoid cells are analyzed using the IL-22 Secretion Assay starting from whole blood, peripheral blood mononuclear cells (PBMCs), or other lymphocyte-containing single cell preparations. Interleukin 22 (IL-22) is a pro-inflammatory cytokine of the IL-10 superfamily. As such it is essential for the stimulation of inflammatory responses. Acting mainly on non-hematopoietic cells, such as hepatocytes, keratinocytes, and lung and intestinal epithelial cells and is known to be expressed in many chronic inflammatory conditions, including Psoriasis and rheumatoid arthritis. However, depending on the inflammatory context, IL-22 also has a protective role in inflammation and in tissue repair. IL-22 is expressed by both the adaptive arm of the immune system, such as CD4

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T cell subsets, as well as by innate lymphocytes, including NK cells, lymphoid tissue inducer (LTi) and LTi-like cells.

Downstream applications

The IL-22 Secretion Assay – Cell Detection and Enrichment Kit (PE) is used for the enrichment and detection of viable human IL-22-secreting cells.

Applications include:

Enrichment and detection of viable IL-22–secreting lymphocytes from whole blood. The IL-22 Secretion Assay can be started directly from whole blood. For details on the procedure refer to www.miltenyibiotec.com/protocols.
Enrichment and detection of IL-22–secreting cells for enumeration and phenotypic characterization as well as for expansion and functional characterization.
Isolation and expansion of IL-22–secreting T cells.
Enrichment and analysis of IL-22–secreting cells for determination of functional characteristics in inflammation, autoimmunity, and in the context of inflammatory protection and tissue repair.

Columns

MS, LS, or autoMACS

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Columns.

Data and images