CD93 MicroBeads have been developed for the separation of mouse cells based on the expression of the CD93 antigen.

Data and images for CD93 MicroBeads, mouse

Figures

Figure 1

CD93
+
cells were isolated from mouse bone marrow (A) or mouse fetal liver (B) using CD93 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD93-APC and Labeling Check Reagent-FITC 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) Bone marrow
Before isolation:
After isolation:
View details

Figure 1

CD93
+
cells were isolated from mouse bone marrow (A) or mouse fetal liver (B) using CD93 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD93-APC and Labeling Check Reagent-FITC 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

CD93
+
cells were isolated from mouse bone marrow (A) or mouse fetal liver (B) using CD93 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD93-APC and Labeling Check Reagent-FITC 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) Fetal liver
Before isolation:
After isolation:
View details

Figure 1

CD93
+
cells were isolated from mouse bone marrow (A) or mouse fetal liver (B) using CD93 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD93-APC and Labeling Check Reagent-FITC 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

CD93
+
cells were isolated from mouse bone marrow (A) or mouse fetal liver (B) using CD93 MicroBeads, an MS Column, and a MiniMACS™ Separator. Cells were fluorescently stained with CD93-APC and Labeling Check Reagent-FITC 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 CD93 MicroBeads, mouse

Overview

CD93 MicroBeads have been developed for the separation of mouse cells based on the expression of the CD93 antigen.

Detailed product information

Background information

CD93 is predominantly expressed on B cell progenitor cells in the bone marrow of adult mice and the fetal liver of unborn mice.

Columns

For positive selection: MS, LS, or XS Columns. For depletion: LD, CS, or D Columns. Cells that strongly express the CD93 antigen can also be depleted using MS, LS, or XS Columns. Positive selection or depletion can also be performed by using the autoMACS
®
Pro Separator or the MultiMACS™ Cell24 Separator.

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CD93 MicroBeads, mouse

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