n418 biorad cat Search Results


n418 biorad cat  (Bio-Rad)
93
Bio-Rad n418 biorad cat
N418 Biorad Cat, 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/product/n418+biorad+cat/Hamster+anti+Mouse+CD11c/pm41421352-627-83-84
Average 93 stars, based on 1 article reviews
n418 biorad cat - by Bioz Stars, 2026-09
93/100 stars
  Buy from Supplier
nk1.1 antibody / cd161c  (NSJ Bioreagents)
99
NSJ Bioreagents nk1.1 antibody / cd161c
Nk1.1 Antibody / Cd161c, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/n418+biorad+cat/Nk1%2E1+Antibody+%2F+Cd161c/custom%40v8986%4036470865
Average 99 stars, based on 1 article reviews
nk1.1 antibody / cd161c - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier
cd301 apc  (Bio-Rad)
94
Bio-Rad cd301 apc
Cd301 Apc, 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/product/n418+biorad+cat/Rat+anti+Mouse+CD301/pmc09927046-66-6-10
Average 94 stars, based on 1 article reviews
cd301 apc - by Bioz Stars, 2026-09
94/100 stars
  Buy from Supplier
cd64 pe  (Becton Dickinson)
90
Becton Dickinson cd64 pe
Male Msr1KO mice have decreased fat mass and inflammation compared to non-littermate wild-type controls. ( a ) Whole body weight for 12-week HFD fed Msr1KO (red) and C57BL6 wild type non-littermate controls (white). ( b ) Organ weight for Msr1KO (red) and WT non-littermate controls (black). ( c ) Insulin tolerance test (ITT) after 12 weeks of HFD. Flow cytometry analysis of ( d ) CD45 + leukocytes, ( e ) <t>CD64</t> + ATMs, ( f ) CD64 − CD11c + ATDCs, ( g ) CD11c + ATMs, ( h ) CD11c + ATMs, and ( i ) CD64 + Ki67 + ATMs in SVF after 12 weeks of HFD. n = 5/group. * p < 0.05. Statistical Analysis = T-test. Identical results observed when data was expressed as percent total SVF cells.
Cd64 Pe, 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/n418+biorad+cat/cd64+pe+antibody/pmc09927046-66-21-25
Average 90 stars, based on 1 article reviews
cd64 pe - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
cd11b-pe-cy7  (Becton Dickinson)
90
Becton Dickinson cd11b-pe-cy7
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Cd11b Pe Cy7, 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/n418+biorad+cat/anti+cd3/pmc09722918-331-23-25
Average 90 stars, based on 1 article reviews
cd11b-pe-cy7 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
mhcii-bv711  (Becton Dickinson)
90
Becton Dickinson mhcii-bv711
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Mhcii Bv711, 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/n418+biorad+cat/streptavidin+bv711/pmc09722918-331-17-19
Average 90 stars, based on 1 article reviews
mhcii-bv711 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
af647  (Bio-Rad)
96
Bio-Rad af647
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Af647, supplied by Bio-Rad, 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/product/n418+biorad+cat/Rat+anti+Mouse+CD206/pmc12830989-261-37-40
Average 96 stars, based on 1 article reviews
af647 - by Bioz Stars, 2026-09
96/100 stars
  Buy from Supplier
ly6g/6c-apc-cy7  (Becton Dickinson)
90
Becton Dickinson ly6g/6c-apc-cy7
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Ly6g/6c Apc Cy7, 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/n418+biorad+cat/ly6g+antibody/pmc09722918-331-11-13
Average 90 stars, based on 1 article reviews
ly6g/6c-apc-cy7 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
dab substrate kit servicebio cat  (Servicebio Inc)
86
Servicebio Inc dab substrate kit servicebio cat
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Dab Substrate Kit Servicebio Cat, supplied by Servicebio Inc, 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/product/n418+biorad+cat/dab+kit/pm41421352-627-268-271
Average 86 stars, based on 1 article reviews
dab substrate kit servicebio cat - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
oil red o servicebio cat  (Servicebio Inc)
86
Servicebio Inc oil red o servicebio cat
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Oil Red O Servicebio Cat, supplied by Servicebio Inc, 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/product/n418+biorad+cat/alizarin+red+s+solution/pm41421352-627-182-185
Average 86 stars, based on 1 article reviews
oil red o servicebio cat - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
anti marco fitc  (Bio-Rad)
93
Bio-Rad anti marco fitc
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Anti Marco Fitc, 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/product/n418+biorad+cat/Rat+anti+Mouse+MARCO/pm31269444-185-110-114
Average 93 stars, based on 1 article reviews
anti marco fitc - by Bioz Stars, 2026-09
93/100 stars
  Buy from Supplier
anti cd200r  (Bio-Rad)
93
Bio-Rad anti cd200r
a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for <t>CD11b+</t> and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.
Anti Cd200r, 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/product/n418+biorad+cat/Rat+anti+Mouse+CD200R/pm31269444-185-74-77
Average 93 stars, based on 1 article reviews
anti cd200r - by Bioz Stars, 2026-09
93/100 stars
  Buy from Supplier

Image Search Results


Male Msr1KO mice have decreased fat mass and inflammation compared to non-littermate wild-type controls. ( a ) Whole body weight for 12-week HFD fed Msr1KO (red) and C57BL6 wild type non-littermate controls (white). ( b ) Organ weight for Msr1KO (red) and WT non-littermate controls (black). ( c ) Insulin tolerance test (ITT) after 12 weeks of HFD. Flow cytometry analysis of ( d ) CD45 + leukocytes, ( e ) CD64 + ATMs, ( f ) CD64 − CD11c + ATDCs, ( g ) CD11c + ATMs, ( h ) CD11c + ATMs, and ( i ) CD64 + Ki67 + ATMs in SVF after 12 weeks of HFD. n = 5/group. * p < 0.05. Statistical Analysis = T-test. Identical results observed when data was expressed as percent total SVF cells.

Journal: Scientific Reports

Article Title: MSR1 is not required for obesity-associated inflammation and insulin resistance in mice

doi: 10.1038/s41598-023-29736-0

Figure Lengend Snippet: Male Msr1KO mice have decreased fat mass and inflammation compared to non-littermate wild-type controls. ( a ) Whole body weight for 12-week HFD fed Msr1KO (red) and C57BL6 wild type non-littermate controls (white). ( b ) Organ weight for Msr1KO (red) and WT non-littermate controls (black). ( c ) Insulin tolerance test (ITT) after 12 weeks of HFD. Flow cytometry analysis of ( d ) CD45 + leukocytes, ( e ) CD64 + ATMs, ( f ) CD64 − CD11c + ATDCs, ( g ) CD11c + ATMs, ( h ) CD11c + ATMs, and ( i ) CD64 + Ki67 + ATMs in SVF after 12 weeks of HFD. n = 5/group. * p < 0.05. Statistical Analysis = T-test. Identical results observed when data was expressed as percent total SVF cells.

Article Snippet: The following conjugated antibodies were used: CD301 APC (Clone ER-MP23, BioRad, Cat# MCA2392A647), CD45 Pacific Blue (Clone 30-F11, eBiosciences, Cat# 48,045,182), CD64 PE (Clone X54-6/7.1.1, BD Biosciences, Cat# 558,455), CD11c APC-Cy7 (Clone N418, eBiosciences, Cat# 47,011,482), and Ki67 PeCy7 (Clone SolA15, eBiosciences, Cat#25,569,882).

Techniques: Flow Cytometry

a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for CD11b+ and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: The circadian clock influences T cell responses to vaccination by regulating dendritic cell antigen processing

doi: 10.1038/s41467-022-34897-z

Figure Lengend Snippet: a A schematic summarising how ZT time can be inferred from the in vitro synchonised serum shock model comparing Per2 mRNA oscillation in BMDCs. Shading represents the relative active periods. As mice are nocturnal, 12 h post synchronisation represents ZT0 the onset of the inactive phase, whereas 24 h post synchronisation represents ZT12 the onset of the active phase. b Per2::luciferase BMDCs were synchronised by serum shock and circadian rhythms were measured using lumicycle technology ( n = 3 biologically independent samples). Bmal1 +/+ and Bmal1 − / − BMDCs were synchronised and antigen processing was measured at c 4 h or d 12 h intervals over a 48 h time course ( n = 3 independent experiments). Antigen processing was measured by addition of DQ-OVA (1 µg/mL) and fluorescence (blue – DAPI, green – DQ-OVA) was measured at 15 min (uptake) or 60 min (processing) and then fixed and analysed by confocal microscopy. e Spleens were isolated from WT mice at ZT1, ZT7, ZT13 and ZT19 and single cell suspension generated, stained for DQ-OVA (1 μg/mL) as in ( c , d ) and subsequently stained for CD11b+ and CD11c+ and analysed by flow cytometry ( n = 4 mice). f Spleens isolated from Bmal1 myeloid+/+ and Bmal1 myeloid − / − mice and stained for DQ-OVA as in ( c , d ) and CD11b + and analysed by flow cytometry ( n = 3 mice) p = 0.0045. g , h Splenic DCs were expanded by B16-FLT3L cells. g cDCs, cDC1s, cDC2s, plasmacytoid DCs and macrophages, or h migratory and resident DCs were identified by flow cytometry and DQ-OVA processing quantified by flow cytometry ( n = 3–4 mice). cDC p = 0.003, cDC1 p = 0.005, cDC2 p = 0.04, pDC p = 0.02, macs p = 0.001, migratory DCs p = 0.01, resident DCs p = 0.0092 Data shown is mean with error bars representing ± SEM. Luciferase data was analysed for circadian rhythmicity by JTK cycle ( b ). Antigen processing in Bmal1 +/+ was predicted to be circadian by cosinor analysis ( c ). Data were compared by one-way ANOVA with Tukey’s post-hoc test for multiple comparisons ( e ) or by a two-tailed t -test ( f–h ). * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001. Source data are provided as a Source Data file.

Article Snippet: Antibodies used as follows: CD3-APC (145-2c11, Biolegend), F4/80-AF700 (cat. MCA497A700, BioRad), LY6G/6C-APC-Cy7 (RB6-8C5, BD), NK1.1-BV421 (PK136, Biolegend), MHCII-BV711 (M5/114, BD), CD11c-BV785 (N418, Biolegend), CD11b-PE-Cy7 (M1/70, BD), CD45R/B220-V500 (RA3-6B2, BD), CD103-PE (2E7, Invitrogen), CD8-Percp-Cy5.5 (53–6.7, Biolegend) and CD317-BV650 (927, Biolegend).

Techniques: In Vitro, Luciferase, Fluorescence, Confocal Microscopy, Isolation, Generated, Staining, Flow Cytometry, Two Tailed Test