Name: 8-Color Immunophenotyping Kit, human
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Product data and images for 8-Color Immunophenotyping Kit, human

Figures

Figure 1

Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant

^®

Analyzer 10.

As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19

⁺

(G). The remaining cells were separated into CD16

⁺

/SSC

^high

neutrophils, CD16

^–

/SSC

^high

eosinophils as well as a CD16

^–/dim

/SSC

^low

population (H). CD3 and CD56 were used to distinguish CD56

⁺

NK cells, CD3

⁺

T cells and a CD3

⁺

CD56

⁺

T cell population (I). The T cells were divided into CD4

⁺

and CD8

⁺

T cells (J).

A:	B:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
C:	D:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
E:	F:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
G:	H:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
I:	J:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).

Specifications for 8-Color Immunophenotyping Kit, human

Overview

The 8-Color Immunophenotyping Kit simplifies the flow-cytometric evaluation of cell fractions for immunofluorescent staining of whole blood, peripheral mononuclear cells (PBMCs), lysed whole blood samples, or other single-cell suspensions from human tissue. The kit cocktail has been designed for the reliable identification of human monocytes, neutrophils, eosinophils, and T, B, and NK lymphocyte populations as well as CD4

⁺

, CD8

⁺

, and CD56

⁺

CD3

⁺

T cell subsets in human blood.

Detailed product information

Applications

Evaluation of leukocyte subsets in whole blood, PBMCs, lysed whole blood samples, or other single-cell suspensions from human tissue.

Resources for 8-Color Immunophenotyping Kit, human

Documents and Protocols

Scientific posters

Data and images for 8-Color Immunophenotyping Kit, human

Figures

Figure 1

^®

Analyzer 10.

⁺

(G). The remaining cells were separated into CD16

⁺

/SSC

^high

neutrophils, CD16

^–

/SSC

^high

eosinophils as well as a CD16

^–/dim

/SSC

^low

population (H). CD3 and CD56 were used to distinguish CD56

⁺

NK cells, CD3

⁺

T cells and a CD3

⁺

CD56

⁺

T cell population (I). The T cells were divided into CD4

⁺

and CD8

⁺

T cells (J).

A:	B:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
C:	D:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
E:	F:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
G:	H:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).
I:	J:
View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).	View details Figure 1 Whole blood from a healthy donor was stained with the 8-Color Immunophenotyping Kit, human. Staining was carried out at room temperature for 10 minutes. Subsequently, red blood cells were lysed by incubation using 1× Red Blood Cell Lysis Solution at room temperature for 15 minutes. Cells were analyzed by flow cytometry using the MACSQuant ^® Analyzer 10. As a preliminary step for elimination of doublets a gate around single cells in forward scatter area (FSC-A) versus forward scatter height (FSC-H) (A) as well as a gate around viable cells was set (B). To identify the major circulating blood cell types CD45 was used to target all leukocytes (C). Theses cells were further separated from debris via forward scatter (FSC) and side scatter (SSC) (D). Monocytes were discriminated based on their CD14 expression (E) and then further divided into classical, intermediate, and non-classical monocytes via CD16 (F). Among the non-monocyte population, B cells were defined as CD19 ⁺ (G). The remaining cells were separated into CD16 ⁺ /SSC ^high neutrophils, CD16 ^– /SSC ^high eosinophils as well as a CD16 ^–/dim /SSC ^low population (H). CD3 and CD56 were used to distinguish CD56 ⁺ NK cells, CD3 ⁺ T cells and a CD3 ⁺ CD56 ⁺ T cell population (I). The T cells were divided into CD4 ⁺ and CD8 ⁺ T cells (J).

Specifications

Specifications for 8-Color Immunophenotyping Kit, human

Overview

⁺

, CD8

⁺

, and CD56

⁺

CD3

⁺

T cell subsets in human blood.

Detailed product information

Applications

Evaluation of leukocyte subsets in whole blood, PBMCs, lysed whole blood samples, or other single-cell suspensions from human tissue.

Resources

Resources for 8-Color Immunophenotyping Kit, human

Documents and Protocols

Scientific posters

8-Color Immunophenotyping Kit, human

8-Color Immunophenotyping Kit, human

Product overview

Product data and images for 8-Color Immunophenotyping Kit, human

Figures

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

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Figure 1

Specifications for 8-Color Immunophenotyping Kit, human

Overview

Detailed product information

Applications

Resources for 8-Color Immunophenotyping Kit, human

Documents and Protocols

Data and images for 8-Color Immunophenotyping Kit, human

Figures

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Figure 1

Specifications for 8-Color Immunophenotyping Kit, human

Overview

Detailed product information

Applications

Resources for 8-Color Immunophenotyping Kit, human

Documents and Protocols

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