sheep cross reactivity Search Results


y3p  (ATCC)
91
ATCC y3p
Y3p, supplied by ATCC, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cross reactivity against bovine il 6  (Bio-Rad)
93
Bio-Rad cross reactivity against bovine il 6
Cross Reactivity Against Bovine Il 6, 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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heart brain lysate cross reactivity varying amounts  (Novus Biologicals)
90
Novus Biologicals heart brain lysate cross reactivity varying amounts
Heart Brain Lysate Cross Reactivity Varying Amounts, supplied by Novus Biologicals, 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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an antibody raised against bovine pgis and having cross reactivity for human pgis  (Cayman Chemical)
90
Cayman Chemical an antibody raised against bovine pgis and having cross reactivity for human pgis
An Antibody Raised Against Bovine Pgis And Having Cross Reactivity For Human Pgis, supplied by Cayman Chemical, 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
an antibody raised against bovine pgis and having cross reactivity for human pgis - by Bioz Stars, 2026-06
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anti mouse igg  (Rockland Immunochemicals)
96
Rockland Immunochemicals anti mouse igg
Anti Mouse Igg, supplied by Rockland Immunochemicals, 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
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cross reactive anti ovine il 8 specific mab  (Bio-Rad)
93
Bio-Rad cross reactive anti ovine il 8 specific mab
Cross Reactive Anti Ovine Il 8 Specific Mab, 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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sheep cross-reactive anti-tlr4 ab  (Becton Dickinson)
90
Becton Dickinson sheep cross-reactive anti-tlr4 ab
Sheep Cross Reactive Anti Tlr4 Ab, 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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anti rat erk1  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology anti rat erk1
Anti Rat Erk1, supplied by Santa Cruz Biotechnology, 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
anti rat erk1 - by Bioz Stars, 2026-06
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an antibody raised against sheep cox-1 and having cross-reactivity for human cox-1  (Cayman Chemical)
90
Cayman Chemical an antibody raised against sheep cox-1 and having cross-reactivity for human cox-1
An Antibody Raised Against Sheep Cox 1 And Having Cross Reactivity For Human Cox 1, supplied by Cayman Chemical, 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/an antibody raised against sheep cox-1 and having cross-reactivity for human cox-1/product/Cayman Chemical
Average 90 stars, based on 1 article reviews
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mouse anti bovine cd4  (Bio-Rad)
94
Bio-Rad mouse anti bovine cd4
FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, <t>CD4,</t> CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).
Mouse Anti Bovine Cd4, 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
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Average 94 stars, based on 1 article reviews
mouse anti bovine cd4 - by Bioz Stars, 2026-06
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mouse anti human cd14  (Bio-Rad)
95
Bio-Rad mouse anti human cd14
FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and <t>CD14</t> are plotted for efferent lymph (C) and peripheral blood (D).
Mouse Anti Human Cd14, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse anti human cd14/product/Bio-Rad
Average 95 stars, based on 1 article reviews
mouse anti human cd14 - by Bioz Stars, 2026-06
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mouse antibovine wc1  (Bio-Rad)
94
Bio-Rad mouse antibovine wc1
FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, <t>WC1,</t> and CD14 are plotted for efferent lymph (C) and peripheral blood (D).
Mouse Antibovine Wc1, 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/mouse antibovine wc1/product/Bio-Rad
Average 94 stars, based on 1 article reviews
mouse antibovine wc1 - by Bioz Stars, 2026-06
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Image Search Results


FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Staining

FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Infection, Labeling, Injection, Staining, Marker

FIG. 8. Percentages of BrdU cells present among efferent lymph cells and PBMCs after intravenous pulses of BrdU. The percentage of BrdU-stained cells, as determined by flow cytometry, is plotted for the total live-cell population as well as within IgM, CD4, CD8, and WC1

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 8. Percentages of BrdU cells present among efferent lymph cells and PBMCs after intravenous pulses of BrdU. The percentage of BrdU-stained cells, as determined by flow cytometry, is plotted for the total live-cell population as well as within IgM, CD4, CD8, and WC1

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Staining, Cytometry

FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Article Snippet: For double labeling, mouse-anti-human CD14 (clone TÜK4, IgG2a isotype; cross-reactive with sheep; Serotec) conjugated to phycoerythrin-Cy5 was used at 1:50.

Techniques: Staining

FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Article Snippet: For double labeling, mouse-anti-human CD14 (clone TÜK4, IgG2a isotype; cross-reactive with sheep; Serotec) conjugated to phycoerythrin-Cy5 was used at 1:50.

Techniques: Infection, Labeling, Injection, Staining, Marker

FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 1. Leukocytes in efferent lymph and peripheral blood of can- nulated, uninfected sheep 455. Cell counts are plotted in thousands per l as a function of time after cannulation for efferent lymph cells (A) and leukocytes (B) (closed symbols) and mononuclear cells (open symbols) from peripheral blood. Percentages of live-gated, mononu- clear cells staining for the surface markers IgM, CD4, CD8, WC1, and CD14 are plotted for efferent lymph (C) and peripheral blood (D).

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Staining

FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 5. Cell lineages and blasts among efferent lymph cells of mock-infected and infected sheep. (A) Percentages of live cell labeling on the surface for IgM, CD4, CD8, WC1, and CD14 are plotted for each animal relative to the day of injection with allogeneic cells. Horizontal reference lines represent the average percentage for a given lineage as measured in each animal before injection of allogeneic cells. (B) Reciprocal oscillation of IgM and CD8 lymph cells in infected, cannulated sheep. (C) Percentages of blasts among lymph cells of different lineages. Blasts were quantified as percentages of lymph cells staining for the indicated surface marker by gating on cells with high forward and side scatter (infected animals, closed symbols; mock-infected animals, open symbols). Averages for infected (solid lines) and mock-infected (dotted lines) animals were calculated using measurements made either on the same day or on adjacent days after injection of allogeneic cells.

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Infection, Labeling, Injection, Staining, Marker

FIG. 8. Percentages of BrdU cells present among efferent lymph cells and PBMCs after intravenous pulses of BrdU. The percentage of BrdU-stained cells, as determined by flow cytometry, is plotted for the total live-cell population as well as within IgM, CD4, CD8, and WC1

Journal: Journal of Virology

Article Title: Dissemination of Bovine Leukemia Virus-Infected Cells from a Newly Infected Sheep Lymph Node

doi: 10.1128/jvi.00529-06

Figure Lengend Snippet: FIG. 8. Percentages of BrdU cells present among efferent lymph cells and PBMCs after intravenous pulses of BrdU. The percentage of BrdU-stained cells, as determined by flow cytometry, is plotted for the total live-cell population as well as within IgM, CD4, CD8, and WC1

Article Snippet: Primary antibodies to surface proteins were as follows: affinity-purified rabbit-anti-sheep immunoglobulin (Kirkegaard & Perry Laboratories) used at 1:200; mouse-anti-bovine CD4 (clone GC1A, IgG2a isotype; cross-reactive with sheep; Veterinary Medical Research and Development, Inc.) used at 1:50; mouse-anti-bovine CD8 (clone CC63, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50; mouse-antibovine WC1 (clone CC15, IgG2a isotype; cross-reactive with sheep; Serotec) used at 1:50 to detect a major subpopulation of T cells (41); and affinitypurified mouse-anti-sheep CD14 (clone VPM65, IgG1 isotype; Serotec) (16) used at 1:50.

Techniques: Staining, Cytometry