Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
(/μL)
Erythrocyte surface marker test CD55
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
85.4 or less (%)
Erythrocyte surface marker test CD59
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
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 technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
criteria: see below
Leukemia/lymphoma analysis test (LLA)CD45 gating (hematopoietic malignancy cell test)
bone marrow aspirate
1.0
H00
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Leukemia/lymphoma analysis test (LLA)CD45 gating (hematopoietic malignancy cell test)
Blood (heparin added)
5.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
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 technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
PHA-induced lymphocyte stimulation test
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)
ConA-induced lymphocyte stimulation test
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 medical 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)
20.0, 10.0, and 10.0
PH9
9-11
3H-thymidine uptake ability
3H-thymidine uptake ability (3H-TdR uptake) Method. Lymphocytes are cultured with a stimulating substance and 3H-thymidine, and the amount of 3H-thymidine taken into the cells by DNA synthesis is expressed as radioactivity. Measure. PHA, ConA, drugs, etc. are used as stimulants.
T cell percentage B cell percentage
Blood (heparin added)
3.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
T66-89 B4-13(%)
B cell surface immune globulin (Sm-Ig) IgG
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
1-3(%)
B cell surface immune globulin (Sm-Ig) IgA
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
1-3(%)
B cell surface immune globulin (Sm-Ig) IgM
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
3-12(%)
B cell surface immune globulin (Sm-Ig) IgD
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
1-10(%)
B cell surface immune globulin (Sm-Ig) K
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
3-8(%)
B cell surface immune globulin (Sm-Ig) L
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
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 technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
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 technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
See below
IgG-FcR+・T cell percentage
Blood (heparin added)
1.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
2-23(%)
Platelet surface marker test CD41
Blood (heparin added)
5.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
97.0 or less (%)
Platelet surface marker test CD42b
Blood (heparin added)
5.0
PH5
3-5
Flow cytometry(FCM)
Flow cytometry A technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
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 technique for analysis of individual cells. Cells stained with fluorochrome-labeled monoclonal antibodies are flown in a stream of solution at a high speed and are passed through the laser beam. The cells are individually analyzed by forward scatter (size of the cell), 90° side scatter (internal complexity of the cell), and fluorescence intensity (cell surface expression of the antigen). Two-color flow cytometry uses a combination of fluorochromes for double staining.
Notifications of URL changes/lab information added
You can now view test items from all labs.
Please choose a lab from the list below.
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.
Notifications of URL changes/lab information added
You can now view test items from all labs.
Please choose a lab from the list below.
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.
