mouse ly6c apc Search Results


anti mouse ly6c flow cytometry monoclonal clone monts1 apc  (Innovative Research Inc)
N/A
Anti Mouse Ly6C Flow Cytometry Monoclonal Clone MONTS1 APC from Innovative Research is a flow cytometry antibody, buffered in PBS with 0.05% Proclin300, 1% BSA. This flow cytometry antibody has been specifically designed to work
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e ab f1120e  (Elabscience Biotechnology)
93
Elabscience Biotechnology e ab f1120e
E Ab F1120e, supplied by Elabscience Biotechnology, 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/product/mouse+ly6c+apc/pmc12533147-179-0-1?v=Elabscience+Biotechnology
Average 93 stars, based on 1 article reviews
e ab f1120e - by Bioz Stars, 2026-08
93/100 stars
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ly6c  (Cytek Biosciences)
92
Cytek Biosciences ly6c
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Ly6c, supplied by Cytek Biosciences, 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/product/mouse+ly6c+apc/pmc11148125-47-37-43?v=Cytek+Biosciences
Average 92 stars, based on 1 article reviews
ly6c - by Bioz Stars, 2026-08
92/100 stars
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anti mouse ly6c apc elabscience  (Elabscience Biotechnology)
93
Elabscience Biotechnology anti mouse ly6c apc elabscience
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Anti Mouse Ly6c Apc Elabscience, supplied by Elabscience Biotechnology, 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/product/mouse+ly6c+apc/pm39412984-208-32-35?v=Elabscience+Biotechnology
Average 93 stars, based on 1 article reviews
anti mouse ly6c apc elabscience - by Bioz Stars, 2026-08
93/100 stars
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5931 u100  (Cytek Biosciences)
92
Cytek Biosciences 5931 u100
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
5931 U100, supplied by Cytek Biosciences, 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/product/mouse+ly6c+apc/pmc10619500-247-61-59?v=Cytek+Biosciences
Average 92 stars, based on 1 article reviews
5931 u100 - by Bioz Stars, 2026-08
92/100 stars
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anti-mouse ly6c (hk1-4)-apc/cy7  (Sony)
90
Sony anti-mouse ly6c (hk1-4)-apc/cy7
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Anti Mouse Ly6c (Hk1 4) Apc/Cy7, supplied by Sony, 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/product/mouse+ly6c+apc/pm37491334-268-15-18?v=Sony
Average 90 stars, based on 1 article reviews
anti-mouse ly6c (hk1-4)-apc/cy7 - by Bioz Stars, 2026-08
90/100 stars
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allophycocyanin conjugated anti mouse ly 6c al 21  (Becton Dickinson)
90
Becton Dickinson allophycocyanin conjugated anti mouse ly 6c al 21
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Allophycocyanin Conjugated Anti Mouse Ly 6c Al 21, 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
https://www.bioz.com/product/mouse+ly6c+apc/pmc06692579-139-21-26?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
allophycocyanin conjugated anti mouse ly 6c al 21 - by Bioz Stars, 2026-08
90/100 stars
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apc anti-mouse ly6 c  (Becton Dickinson)
90
Becton Dickinson apc anti-mouse ly6 c
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Apc Anti Mouse Ly6 C, 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
https://www.bioz.com/product/mouse+ly6c+apc/pmc06136871-439-66-70?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
apc anti-mouse ly6 c - by Bioz Stars, 2026-08
90/100 stars
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ly-6c antibody, anti-mouse  (Miltenyi Biotec)
94
Miltenyi Biotec ly-6c antibody, anti-mouse
The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes <t>(Ly6C</t> + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).
Ly 6c Antibody, Anti Mouse, 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/product/mouse+ly6c+apc/custom%40130-123-285%4029984041?v=Miltenyi+Biotec
Average 94 stars, based on 1 article reviews
ly-6c antibody, anti-mouse - by Bioz Stars, 2026-08
94/100 stars
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apc cy 7 rat anti mouse ly 6g and ly 6c  (BD Biosciences)
N/A
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apc anti mouse ly 6g ly 6c gr 1 antibody  (Elabscience)
N/A
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apc/cy7 anti-mouse ly-6c  (BioLegend)
N/A
APC/Cy7 anti-mouse Ly-6C [HK1.4]; Isotype: Rat IgG2c, κ; Reactivity: Mouse; Apps: FC; Size: 25 μg
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Image Search Results


The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes (Ly6C + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).

Journal: FEBS Open Bio

Article Title: Neutrophil and macrophage crosstalk might be a potential target for liver regeneration

doi: 10.1002/2211-5463.13803

Figure Lengend Snippet: The interaction between neutrophils and macrophages enhances liver regeneration. (A) Network diagrams showing cell–cell interactions indicated by arrows (edges) pointing in the source‐to‐target direction. The thickness indicates the sum of the weighted paths between populations, and the color of the arrows corresponds to the source. Network diagrams for clusters 10–18 are shown. (B) Flow cytometry was used to determine the percentage of macrophages (F4/80 + CD11b + ) in total immune cells (CD45 + ) in the different groups ( n = 6, * P < 0.05). (C) Flow cytometry revealed the percentage of Kupffer cells (CLEC4F + ) in macrophages in the different groups (F4/80 + CD11b + CD45 + ) ( n = 6, * P < 0.05). (D) Flow cytometry revealed the percentage of monocytes (Ly6C + CD11b + ) among the total immune cells in the different groups (CD45+) ( n = 6, * P < 0.05). (E) The mRNA expression levels of Ccl3, Ccl5 and Cxcl1 were examined using qPCR analysis (the genes were normalized to GAPDH mRNA levels in each sample. Ccl3, C‐C motif chemokine ligand 3; Ccl5, C‐C motif chemokine ligand 5; Cxcl1, C‐X‐C motif chemokine ligand 1; n = 3, * P < 0.05). (F) Macrophages cultured without neutrophils and co‐culture of neutrophils and macrophages ( n = 3, * P < 0.05).

Article Snippet: Primary antibodies against CD45 (dilution 1 : 100; 75‐0451‐U100; TONBO, Tokyo, Japan), CD11b (dilution 1 : 100; 85‐0112‐U100; TONBO), Ly6G (dilution 1 : 100; 127633; BioLegend, San Diego, CA, USA), F4/80 (dilution 1 : 100; 123137; BioLegend), LY6C (dilution 1 : 100; 20‐5932‐U100; TONBO) and CLEC4F (dilution 1 : 100; 156804; BioLegend) were carried out in FACS buffer (4 °C for 60 min).

Techniques: Flow Cytometry, Expressing, Cell Culture, Co-Culture Assay