CD23 MicroBeads were developed for the positive selection or depletion of mouse B cell subsets from various lymphoid tissues based on the expression of the CD23 antigen.

Data and images for CD23 MicroBeads, mouse

Figures

Figure 1

CD23
+
cells were isolated from mouse spleen (A) or mouse bone marrow (B) using CD23 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD23-PE (# 130-097-819) and CD45R (B220)-APC (# 130-091-843) and analyzed by flow cytometry using the MACSQuant
®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.
A:
View details

Figure 1

CD23
+
cells were isolated from mouse spleen (A) or mouse bone marrow (B) using CD23 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD23-PE (# 130-097-819) and CD45R (B220)-APC (# 130-091-843) and analyzed by flow cytometry using the MACSQuant
®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.
View details

Figure 1

CD23
+
cells were isolated from mouse spleen (A) or mouse bone marrow (B) using CD23 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD23-PE (# 130-097-819) and CD45R (B220)-APC (# 130-091-843) and analyzed by flow cytometry using the MACSQuant
®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.
B:
View details

Figure 1

CD23
+
cells were isolated from mouse spleen (A) or mouse bone marrow (B) using CD23 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD23-PE (# 130-097-819) and CD45R (B220)-APC (# 130-091-843) and analyzed by flow cytometry using the MACSQuant
®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.
View details

Figure 1

CD23
+
cells were isolated from mouse spleen (A) or mouse bone marrow (B) using CD23 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD23-PE (# 130-097-819) and CD45R (B220)-APC (# 130-091-843) and analyzed by flow cytometry using the MACSQuant
®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.

Specifications for CD23 MicroBeads, mouse

Overview

CD23 MicroBeads were developed for the positive selection or depletion of mouse B cell subsets from various lymphoid tissues based on the expression of the CD23 antigen.

Detailed product information

Background information

CD23 is mainly expressed on follicular (CD93
-
) and transitional B cells (CD93
+
).

Columns

For positive selection: MS, LS, XS, or autoMACS
®
Columns. For depletion: LD, D, or autoMACS Columns.

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CD23 MicroBeads, mouse

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