horse anti mouse antibody Search Results


96
Vector Laboratories vectastain abc kit
Vectastain Abc Kit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
vectastain abc kit - by Bioz Stars, 2026-03
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96
Vector Laboratories biotinylated secondary antibody
Biotinylated Secondary Antibody, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
biotinylated secondary antibody - by Bioz Stars, 2026-03
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95
Vector Laboratories pre diluted horse anti mouse immunoglobulin g conjugated to peroxidase
Pre Diluted Horse Anti Mouse Immunoglobulin G Conjugated To Peroxidase, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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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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93
Vector Laboratories anti mouse
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, supplied by Vector Laboratories, 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/anti mouse/product/Vector Laboratories
Average 93 stars, based on 1 article reviews
anti mouse - by Bioz Stars, 2026-03
93/100 stars
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96
Vector Laboratories anti mouse igg
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 Igg, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti mouse igg/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
anti mouse igg - by Bioz Stars, 2026-03
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93
Vector Laboratories mouse igg conjugated to texas red
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.
Mouse Igg Conjugated To Texas Red, supplied by Vector Laboratories, 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/mouse igg conjugated to texas red/product/Vector Laboratories
Average 93 stars, based on 1 article reviews
mouse igg conjugated to texas red - by Bioz Stars, 2026-03
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96
Vector Laboratories immpress system
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.
Immpress System, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/immpress system/product/Vector Laboratories
Average 96 stars, based on 1 article reviews
immpress system - by Bioz Stars, 2026-03
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93
Vector Laboratories anti mouse secondary antibody
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 Secondary Antibody, supplied by Vector Laboratories, 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/anti mouse secondary antibody/product/Vector Laboratories
Average 93 stars, based on 1 article reviews
anti mouse secondary antibody - by Bioz Stars, 2026-03
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91
Bio-Rad mouse anti horse iggb
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.
Mouse Anti Horse Iggb, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse anti horse iggb/product/Bio-Rad
Average 91 stars, based on 1 article reviews
mouse anti horse iggb - by Bioz Stars, 2026-03
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93
Bio-Rad mouse anti horse cd4
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.
Mouse Anti Horse Cd4, 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/mouse anti horse cd4/product/Bio-Rad
Average 93 stars, based on 1 article reviews
mouse anti horse cd4 - 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