anti cd5 Search Results


cd5  (Miltenyi Biotec)
94
Miltenyi Biotec cd5
Cd5, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd5/product/Miltenyi Biotec
Average 94 stars, based on 1 article reviews
cd5 - by Bioz Stars, 2026-03
94/100 stars
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fluorescein isothiocyanate fitc conjugated mouse anti horse cd5  (Bio-Rad)
94
Bio-Rad fluorescein isothiocyanate fitc conjugated mouse anti horse cd5
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Fluorescein Isothiocyanate Fitc Conjugated Mouse Anti Horse Cd5, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fluorescein isothiocyanate fitc conjugated mouse anti horse cd5/product/Bio-Rad
Average 94 stars, based on 1 article reviews
fluorescein isothiocyanate fitc conjugated mouse anti horse cd5 - by Bioz Stars, 2026-03
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cd5  (Bio-Rad)
93
Bio-Rad cd5
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Cd5, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd5/product/Bio-Rad
Average 93 stars, based on 1 article reviews
cd5 - by Bioz Stars, 2026-03
93/100 stars
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dog cd5  (Bio-Rad)
93
Bio-Rad dog cd5
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Dog Cd5, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/dog cd5/product/Bio-Rad
Average 93 stars, based on 1 article reviews
dog cd5 - by Bioz Stars, 2026-03
93/100 stars
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anti mouse cd5 146nd  (fluidigm)
92
fluidigm anti mouse cd5 146nd
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Anti Mouse Cd5 146nd, supplied by fluidigm, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti mouse cd5 146nd/product/fluidigm
Average 92 stars, based on 1 article reviews
anti mouse cd5 146nd - by Bioz Stars, 2026-03
92/100 stars
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cd5 pe vio770 miltenyi biotec 130 111 109 rea782  (Miltenyi Biotec)
94
Miltenyi Biotec cd5 pe vio770 miltenyi biotec 130 111 109 rea782
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Cd5 Pe Vio770 Miltenyi Biotec 130 111 109 Rea782, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd5 pe vio770 miltenyi biotec 130 111 109 rea782/product/Miltenyi Biotec
Average 94 stars, based on 1 article reviews
cd5 pe vio770 miltenyi biotec 130 111 109 rea782 - by Bioz Stars, 2026-03
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rat anti mouse intercellular adhesion molecule 1 icam 1  (Bio-Rad)
93
Bio-Rad rat anti mouse intercellular adhesion molecule 1 icam 1
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Rat Anti Mouse Intercellular Adhesion Molecule 1 Icam 1, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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flow cytometry anti human cd5 apc tonbo biosciences mouse 20 0059 t100 ucht2  (Cytek Biosciences)
90
Cytek Biosciences flow cytometry anti human cd5 apc tonbo biosciences mouse 20 0059 t100 ucht2
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Flow Cytometry Anti Human Cd5 Apc Tonbo Biosciences Mouse 20 0059 T100 Ucht2, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/flow cytometry anti human cd5 apc tonbo biosciences mouse 20 0059 t100 ucht2/product/Cytek Biosciences
Average 90 stars, based on 1 article reviews
flow cytometry anti human cd5 apc tonbo biosciences mouse 20 0059 t100 ucht2 - by Bioz Stars, 2026-03
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antigens cd5  (Miltenyi Biotec)
94
Miltenyi Biotec antigens cd5
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Antigens Cd5, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antigens cd5/product/Miltenyi Biotec
Average 94 stars, based on 1 article reviews
antigens cd5 - by Bioz Stars, 2026-03
94/100 stars
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ucht2  (fluidigm)
93
fluidigm ucht2
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Ucht2, supplied by fluidigm, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
ucht2 - by Bioz Stars, 2026-03
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biotin antibody cocktail  (Miltenyi Biotec)
94
Miltenyi Biotec biotin antibody cocktail
Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and <t>fluorescein</t> <t>isothiocyanate</t> <t>(FITC)</t> channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against <t>CD5</t> (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.
Biotin Antibody Cocktail, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
biotin antibody cocktail - by Bioz Stars, 2026-03
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Image Search Results


Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and fluorescein isothiocyanate (FITC) channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against CD5 (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.

Journal: Veterinary pathology

Article Title: Flow cytometric analysis of equine bronchoalveolar lavage fluid cells in horses with and without severe equine asthma.

doi: 10.1177/03009858211042588

Figure Lengend Snippet: Figure 5. Flow cytometric analysis of equine bronchoalveolar lavage fluid (BALF) leukocytes. (a) Indicates that cells from p1 have higher forward scatter (FSC) and side scatter (SSC) than cells from p2, indicating they are larger and more internally complex. (b) Unstained control sample showing that many (red circle) but not all cells from p1 (upper panel) have autofluorescence in the phycoerythrin (PE) and fluorescein isothiocyanate (FITC) channels. However, cells from p2 (lower panel) are not autofluorescent. (c) Using anti-CD90 (neutrophil marker) and anti-CD206 (macrophage marker) antibodies, cells from p1 (upper panel) but not p2 (lower panel) are identified as neutrophils (Q3) and macrophages (Q1), respectively. (d) Using antibodies against CD5 (lymphocyte marker) and PanB cells, cells in p1 (upper panel) are double- negative, and cells in p2 (lower panel) are identified as lymphocytes; the red circle indicates autofluorescent cells.

Article Snippet: The fluorescent primary antibodies used in this study were phycoerythrin (PE) conjugated mouse antihuman CD206 (clone 3.29B1, Beckman Coulter), fluorescein isothiocyanate (FITC) conjugated mouse anti-horse CD5 (clone CVS5, Bio-Rad), and PE conjugated mouse anti-horse PanB cells (clone CVS36, Bio-Rad).

Techniques: Control, Marker