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As a global market leader with numerous subsidiaries and distributors, Miltenyi Biotec is committed to providing our customers around the world with the highest quality products. In addition to direct selling in more than 20 countries in North America, Europe and Asia/Pacific, Miltenyi Biotec also provides support for our customers through an extensive distributor network covering dozens of additional countries.
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Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Clone | MJ7/18 |
---|---|
Clonality | monoclonal |
Isotype | rat IgG2aκ |
Isotype control | Isotype Control Antibody, rat IgG2a |
Host | rat |
Type of antibody | Primary antibodies |
Species | mouse |
Antigen | CD105 |
Alternative names of antigen | ENG, Endo, S-endoglin |
Molecular mass of antigen [kDa] | 67 |
Distribution of antigen | endothelial cells, monocytes, stem cells, mesenchymal stem cells, leukemia cells, bone marrow |
Entrez Gene ID | 13805 |
RRID | AB_2660090, AB_2660091, AB_2660092, AB_2660093, AB_2660094, AB_2660095, AB_2660096, AB_2660097, AB_2660098, AB_2660099, AB_2660100, AB_2660101, AB_1103219 |
This antibody is good for MSCs phenotype. MSCs should be positive for CD105 and this antibody works well for this purpose.
This antibody is good for the identification for mesenchymal stem cells isolated from bone marrow, fat and other tissues and is recommended for MSCs phenotype analysis.
Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. | Figure 1Bone marrow cells from BALB/c mice were stained with CD105 antibodies or with the corresponding isotype control (left image) as well as with Anti- Sca-1 antibodies. Flow cytometry was performed using the MACSQuant ® Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence. |
Clone | MJ7/18 |
---|---|
Clonality | monoclonal |
Isotype | rat IgG2aκ |
Isotype control | Isotype Control Antibody, rat IgG2a |
Host | rat |
Type of antibody | Primary antibodies |
Species | mouse |
Antigen | CD105 |
Alternative names of antigen | ENG, Endo, S-endoglin |
Molecular mass of antigen [kDa] | 67 |
Distribution of antigen | endothelial cells, monocytes, stem cells, mesenchymal stem cells, leukemia cells, bone marrow |
Entrez Gene ID | 13805 |
RRID | AB_2660090, AB_2660091, AB_2660092, AB_2660093, AB_2660094, AB_2660095, AB_2660096, AB_2660097, AB_2660098, AB_2660099, AB_2660100, AB_2660101, AB_1103219 |
This antibody is good for MSCs phenotype. MSCs should be positive for CD105 and this antibody works well for this purpose.
This antibody is good for the identification for mesenchymal stem cells isolated from bone marrow, fat and other tissues and is recommended for MSCs phenotype analysis.
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