cover slips Search Results


li cor black box  (LI-COR)
97
LI-COR li cor black box
Li Cor Black Box, supplied by LI-COR, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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microscope cover slips  (Celprogen Inc)
91
Celprogen Inc microscope cover slips
Microscope Cover Slips, supplied by Celprogen Inc, 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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24 well coverslip bottom plate  (Greiner Bio)
95
Greiner Bio 24 well coverslip bottom plate
24 Well Coverslip Bottom Plate, supplied by Greiner Bio, 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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round coverslips  (World Precision Instruments)
93
World Precision Instruments round coverslips
Round Coverslips, supplied by World Precision Instruments, 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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coverslips  (Carolina Biological)
92
Carolina Biological coverslips
Coverslips, supplied by Carolina Biological, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cover slip coated with fibronectin  (Cosmo Bio USA)
90
Cosmo Bio USA cover slip coated with fibronectin
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
Cover Slip Coated With Fibronectin, supplied by Cosmo Bio USA, 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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coverslip coated with 0.3% hypromellose genteal gel  (Novartis)
90
Novartis coverslip coated with 0.3% hypromellose genteal gel
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
Coverslip Coated With 0.3% Hypromellose Genteal Gel, supplied by Novartis, 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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no. 0 cover slips  (Fisher Scientific)
90
Fisher Scientific no. 0 cover slips
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
No. 0 Cover Slips, supplied by Fisher Scientific, 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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apoptag® plastic cover slips  (Merck & Co)
90
Merck & Co apoptag® plastic cover slips
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
Apoptag® Plastic Cover Slips, supplied by Merck & Co, 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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glass cover slips  (Fisher Scientific)
90
Fisher Scientific glass cover slips
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
Glass Cover Slips, supplied by Fisher Scientific, 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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cover slips imaging menzel gläser  (Menzel Inc)
90
Menzel Inc cover slips imaging menzel gläser
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
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cover slips (24 × ≠1.5)  (Menzel Inc)
90
Menzel Inc cover slips (24 × ≠1.5)
a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a <t>fibronectin-coated</t> plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .
Cover Slips (24 × ≠1.5), supplied by Menzel Inc, 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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Image Search Results


a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a fibronectin-coated plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .

Journal: Communications Biology

Article Title: Uptake of osteoblast-derived extracellular vesicles promotes the differentiation of osteoclasts in the zebrafish scale

doi: 10.1038/s42003-020-0925-1

Figure Lengend Snippet: a Representative flow cytometric analysis of cells in scales at 1 day post-fracture (dpf) from a osterix:mCherry single-transgenic animal. Gated regions indicate the mCh + Hoe high cell fraction and mCh + Hoe low EV fraction. b mCh + Hoe high cells and mCh + Hoe low EVs were displayed in an Annexin-V-FITC vs. Sytox Red dot plot. mCh + Hoe high cells were subdivided into three fractions, “live”, “pre-apoptotic”, and “apoptotic”, whereas mCh + Hoe low EVs were divided into two fractions, “microvesicle” (MV) and “apoptotic body” (AB). c Schematic diagram of in vitro cell culture assays. Kidney marrow cells (KMCs) from trap:GFP single-transgenic zebrafish were co-cultured with OBs, MVs, or ABs from fractured scales of osterix:mCherry single-transgenic zebrafish in a fibronectin-coated plate. At 2 days of co-culture, the number of trap:GFP + cells was counted in each well. Non-co-cultured KMCs were used as a control. d The average number of trap:GFP + cells in each type of wells. Error bars, s.d. ( n = 4 for each group). e Representative images of trap:GF P + cells co-cultured with OBs (left panel), MVs (middle panel), or ABs (right panel). trap:GFP + cells contained OB-derived EVs in the cytoplasm (arrows). Bars, 5 μm. f Schematic diagram of zebrafish rankl locus. gRNA target sites and primer recognition sites are shown in red bars and blue arrows, respectively. g qPCR analysis of rankl in the adult fin of wild type control and rankl gRNA-injected animals. Results from seven individual gRNA-injected animals are shown. Data are mean ± s.d. from three independent experiments. h The average number of trap:GFP + cells in non-co-cultured KMCs (control), or KMCs co-cultured with OBs or EVs from wild type or rankl gRNA-injected animals. Error bars, s.d. ( n = 4 for each group); n.s., no significance; * p < 0.05; ** p < 0.01; *** p < 0.001 by one-way ANOVA followed by Dunnett’s test. Experiments were performed twice with four biological replicates in each group d , h .

Article Snippet: For imaging of cultured cells, cells were plated on a cover slip coated with fibronectin (Cosmo Bio) and were cultured as described above.

Techniques: Transgenic Assay, In Vitro, Cell Culture, Co-Culture Assay, Control, Derivative Assay, Injection