Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
(/μL)
Erythrocyte surface marker test CD55
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
85.4 or less (%)
Erythrocyte surface marker test CD59
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
99.8 or more (%)
Highly sensitive PNH-type blood cell test
Blood (EDTA-2Na added)
5.0
PN5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Malignant lymphoma analysis test 7AAD analysis (hematopoietic organ malignant tumor cell test)
lymph nodes
5×5×5mm
H20
(1 day)
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Lymphocyte rejuvenation test using PHA
Blood (heparin added)
5.0
PH9
7-8
3H-thymidine uptake ability
3H-thymidine uptake capacity (3H-TdR uptake) A method using the phenomenon that lymphocytes become blastic in response to stimulation by non-self antigens. Lymphocytes are cultured with the addition of the stimulants and 3H-thymidine, and the amount of 3H-thymidine incorporated into the cells by DNA synthesis is measured as radioactivity. PHA, ConA, and drugs are used for stimulants.
PHA+ 20500-56800 CONTROL 127-456 (cpm)
Lymphocyte blastogenesis test using Con-A
Blood (heparin added)
5.0
PH9
7-8
3H-thymidine uptake ability
3H-thymidine uptake capacity (3H-TdR uptake) A method using the phenomenon that lymphocytes become blastic in response to stimulation by non-self antigens. Lymphocytes are cultured with the addition of the stimulants and 3H-thymidine, and the amount of 3H-thymidine incorporated into the cells by DNA synthesis is measured as radioactivity. PHA, ConA, and drugs are used for stimulants.
Con-A+ 20300-65700 CONTROL 127-456 (cpm)
Drug-induced lymphocyte stimulation test (DLST)
Blood (heparin added)
1 drug 12.0
PH9
8-10
3H-thymidine uptake ability
3H-thymidine uptake capacity (3H-TdR uptake) A method using the phenomenon that lymphocytes become blastic in response to stimulation by non-self antigens. Lymphocytes are cultured with the addition of the stimulants and 3H-thymidine, and the amount of 3H-thymidine incorporated into the cells by DNA synthesis is measured as radioactivity. PHA, ConA, and drugs are used for stimulants.
Negative
MLC (mixed lymphocyte culture)
(Recipient) Blood (heparin addition) and (Donor) Blood (heparin addition) and (Unrelated person) Blood (heparin addition)
(Recipient) 20.0 and (Donor) 10.0 and (Unrelated person) 10.0
PH9
9-11
3H-thymidine uptake ability
3H-thymidine uptake capacity (3H-TdR uptake) A method using the phenomenon that lymphocytes become blastic in response to stimulation by non-self antigens. Lymphocytes are cultured with the addition of the stimulants and 3H-thymidine, and the amount of 3H-thymidine incorporated into the cells by DNA synthesis is measured as radioactivity. PHA, ConA, and drugs are used for stimulants.
T cell percentage B cell percentage
Blood (heparin added)
3.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
T 66-89 B 4-13 (%)
B cell surface immune globulin (Sm-Ig) IgG
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
1-3(%)
B cell surface immune globulin (Sm-Ig) IgA
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
1-3(%)
B cell surface immune globulin (Sm-Ig) IgM
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
3-12(%)
B cell surface immune globulin (Sm-Ig) IgD
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
1-10(%)
B cell surface immune globulin (Sm-Ig) K
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
3-8(%)
B cell surface immune globulin (Sm-Ig) L
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
1-5(%)
Automatic analysis of lymphocyte surface markers using monoclonal antibodies
Blood (heparin added)
3.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
See below
Lymphocyte surface marker test using two-color analysis
Blood (heparin added)
3.0
PH5
3-5
Two-color flow cytometry
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
See below
IgG-FcR+・ T-cell percentage
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
2-23(%)
Platelet surface marker test CD41
Blood (heparin added)
5.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
97.0 or less (%)
Platelet surface marker test CD42b
Blood (heparin added)
5.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
74.9 or less (%)
Th1/Th2(IFN-γ×IL-4/CD4)
Blood (heparin added)
3.0
PH5
4-6
Flow cytometry(FCM)
Flow cytometry A method to analyze individual cells from forward scattered light (cell size), 90° scattered light (internal cell structure) and fluorescence intensity (corresponding antigen on the cell surface) by irradiating cells, which are stained with a monoclonal antibody labeled with a fluorescent dye, with laser light while flowing at high speed. When performing double staining and analysis using two types of fluorescent dyes, it is called two-color flow cytometry.
Notifications of URL changes/lab information added
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Notifications of URL changes/lab information added
You can now view test items from all labs.
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You can switch between labs as any time using the upper right lab icon.
The domain name of the TEST DIRECTORYpage has changed.
Please update bookmarks and saved links with the new address.