data (dsi) telemetry device l21 Search Results


dsi telemetry device l21  (Data Sciences International)
86
Data Sciences International dsi telemetry device l21
Dsi Telemetry Device L21, supplied by Data Sciences International, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/dsi telemetry device l21/product/Data Sciences International
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dsi telemetry device l21 - by Bioz Stars, 2026-06
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bm-mscs lonza 22  (Lonza)
90
Lonza bm-mscs lonza 22
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Bm Mscs Lonza 22, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bm-mscs lonza 22 - by Bioz Stars, 2026-06
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ag/agcl/ kcl 3.00 mol l21 reference electrode  (Metrohm AG)
90
Metrohm AG ag/agcl/ kcl 3.00 mol l21 reference electrode
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Ag/Agcl/ Kcl 3.00 Mol L21 Reference Electrode, supplied by Metrohm AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
ag/agcl/ kcl 3.00 mol l21 reference electrode - by Bioz Stars, 2026-06
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bacto tryptone  (Becton Dickinson)
90
Becton Dickinson bacto tryptone
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Bacto Tryptone, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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ultrapure 2 mol l21 hno3  (SEASTAR CHEMICALS)
90
SEASTAR CHEMICALS ultrapure 2 mol l21 hno3
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Ultrapure 2 Mol L21 Hno3, supplied by SEASTAR CHEMICALS, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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haemoglobin l21 becton dickinson  (Becton Dickinson)
90
Becton Dickinson haemoglobin l21 becton dickinson
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Haemoglobin L21 Becton Dickinson, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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aqueous solution of 33.608 g l21 of potassium dichromate  (PanReac AppliChem)
90
PanReac AppliChem aqueous solution of 33.608 g l21 of potassium dichromate
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Aqueous Solution Of 33.608 G L21 Of Potassium Dichromate, supplied by PanReac AppliChem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rnasin  (Promega)
90
Promega rnasin
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Rnasin, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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glua2 m clone l21/32 1:500  (NeuroMab)
90
NeuroMab glua2 m clone l21/32 1:500
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Glua2 M Clone L21/32 1:500, supplied by NeuroMab, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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oxidizing mineral acid hno3 70  (Univar USA Inc)
90
Univar USA Inc oxidizing mineral acid hno3 70
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Oxidizing Mineral Acid Hno3 70, supplied by Univar USA Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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hbmscs-gfp  (Cyagen Biosciences)
90
Cyagen Biosciences hbmscs-gfp
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
Hbmscs Gfp, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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10 g tryptone l21  (BioLife Solutions)
90
BioLife Solutions 10 g tryptone l21
Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from <t>L21</t> (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.
10 G Tryptone L21, supplied by BioLife Solutions, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from L21 (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.

Journal: Regenerative Therapy

Article Title: Secreted matrix metalloproteinase-14 is a predictor for antifibrotic effect of IC-2-engineered mesenchymal stem cell sheets on liver fibrosis in mice

doi: 10.1016/j.reth.2021.08.004

Figure Lengend Snippet: Characterization of cell surface markers of MSCs by flow cytometry. (a) Representative histogram of the FACS of cell surface marker expression on BM-MSCs used in the present study. BM-MSCs from Lonza 22, Lonza 26, and Lonza 30 at passage 3 were labeled with FITC-coupled antibodies against CD34, CD45, CD90, CD105, and HLA-DR. Shaded areas indicated staining with antibodies against the indicat antigens, and solid lines indicate background fluorescence stained with isotype control. (b) Grouped bar chart showing quantitation of cell surface markers on each lot of three donors-derived BM-MSCs. The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from L21 (Lonza 21) to L30 (Lonza 30). Cell culture was started at a cell density of 5.0 × 10 3 to 1.0 × 10 4 cells/cm 2 (P0) and passaged every 3–4 days to P1, P2, and P3.

Article Snippet: The data are presented as mean ± SD from three independent FACS analyses. (c) The growth curve of the ten lots of BM-MSCs from L21 (Lonza 21) to L30 (Lonza 30).

Techniques: Flow Cytometry, Marker, Expressing, Labeling, Staining, Fluorescence, Control, Quantitation Assay, Derivative Assay, Cell Culture