pre heated sodium citrate buffer Search Results


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New England Biolabs pre heat buffer c
Pre Heat Buffer C, supplied by New England Biolabs, 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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Buffer D, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad pbs pre hybridization solution hs
Pbs Pre Hybridization Solution Hs, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad sodium dodecyl sulfate polyacrylamide gel electrophoresis
Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis, supplied by Bio-Rad, 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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GE Healthcare inactivated fetal bovine serum
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Qiagen qiaquick pcr purification kit
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Bio SB Inc anti-s100-β rabbit monoclonal antibodies clone ep32
Patient characteristics and clinical findings in USP6::MYH9 fusion cases
Anti S100 β Rabbit Monoclonal Antibodies Clone Ep32, supplied by Bio SB 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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MasterTech Inc oil red o staining solution
Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil <t>Red</t> <t>O</t> <t>staining</t> of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.
Oil Red O Staining Solution, supplied by MasterTech 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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GE Healthcare metal affinity chromatography imac buffer
Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil <t>Red</t> <t>O</t> <t>staining</t> of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.
Metal Affinity Chromatography Imac Buffer, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher pre hybridization buffer
Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil <t>Red</t> <t>O</t> <t>staining</t> of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.
Pre Hybridization Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher pre cooled phosphate buffer sodium
Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil <t>Red</t> <t>O</t> <t>staining</t> of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.
Pre Cooled Phosphate Buffer Sodium, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biogenix Inc sodium citrate buffer (ph 6.0
Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil <t>Red</t> <t>O</t> <t>staining</t> of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.
Sodium Citrate Buffer (Ph 6.0, supplied by Biogenix 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


Patient characteristics and clinical findings in USP6::MYH9 fusion cases

Journal: Journal of Clinical Pathology

Article Title: Unusual fusion gene rearrangements in patients with nodular fasciitis: a study of rare and novel USP6 fusion partners with a review of the literature

doi: 10.1136/jcp-2023-208768

Figure Lengend Snippet: Patient characteristics and clinical findings in USP6::MYH9 fusion cases

Article Snippet: Thin histological sections (3 μm thick) were used, and each sample was stained using the following antibodies and protocols: anti-smooth muscle actin (SMA) mouse monoclonal antibodies (clone 1A4, BioSB— Bioscience for the World, dilution 1:75; pretreatment: heating up to 99°C in a pH 6 buffer in a water bath); anti-H-caldesmon mouse monoclonal antibodies (clone BSB-19|, BioSB, dilution 1:100; pretreatment: heating up to 99°C in a pH 9 buffer in a water bath); anti-desmin mouse monoclonal antibodies (clone D33, BioSB, dilution 1:100; pretreatment: heating up to 99°C in a pH 9 buffer in a water bath); anti-S100-β rabbit monoclonal antibodies (clone EP32, BioSB, dilution 1:300; pre-treatment: heating up to 99 ◦C in a pH 9 buffer in a water bath); anti-Ki-67 mouse monoclonal antibodies (clone MIB-1, BioSB, dilution 1:150; pretreatment: heating up to 99°C in a pH 6 buffer in a water bath).

Techniques:

Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil Red O staining of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.

Journal: Communications Biology

Article Title: DIAPH1 mediates progression of atherosclerosis and regulates hepatic lipid metabolism in mice

doi: 10.1038/s42003-023-04643-2

Figure Lengend Snippet: Ldlr − / − and Ldlr − / − Diaph1 − / − male mice were fed Western Diet (WD) for 16 weeks. a Representative images of en face Oil Red O staining of aortas. Quantification of plaque area as percentage of Oil Red O-stained area over total aortic surface area is shown. b – e Representative images of aortic arch sections are shown and quantified for the following: b H&E; c Oil Red O; d CD68; and e , Picrosirius Red. In d , the secondary antibody-alone control is shown. Scale bar: 250 µm. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P values were determined by unpaired T-test.

Article Snippet: Sections were incubated with propylene glycol for 2 min, then incubated with pre-heated Oil Red O staining solution (American MasterTech, STOROPT) at 60 °C for an additional 8 min.

Techniques: Western Blot, Staining

Ldlr − / − and Ldlr − / − Diaph1 −/− male mice were fed WD for 16 weeks. a Representative immunofluorescence staining and quantification of DIAPH1 in the liver of Ldlr −/− and Ldlr −/− Diaph1 −/− male mice. b Representative images of H&E and Oil Red O staining in liver and quantification is shown. c Quantification of free cholesterol content in liver. d Quantification of total cholesterol content in liver. e Quantification of total liver triglycerides. f Representative images of Picrosirius Red staining in liver and quantification is shown. g Quantification of whole liver weight. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. In a the secondary antibody–alone control is shown. Scale bars: 250 µm, and inset boxes: 50 µm. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P- values were determined by unpaired T-test or Wilcoxon rank-sum test depending on if the data passed the Shapiro-Wilk normality test.

Journal: Communications Biology

Article Title: DIAPH1 mediates progression of atherosclerosis and regulates hepatic lipid metabolism in mice

doi: 10.1038/s42003-023-04643-2

Figure Lengend Snippet: Ldlr − / − and Ldlr − / − Diaph1 −/− male mice were fed WD for 16 weeks. a Representative immunofluorescence staining and quantification of DIAPH1 in the liver of Ldlr −/− and Ldlr −/− Diaph1 −/− male mice. b Representative images of H&E and Oil Red O staining in liver and quantification is shown. c Quantification of free cholesterol content in liver. d Quantification of total cholesterol content in liver. e Quantification of total liver triglycerides. f Representative images of Picrosirius Red staining in liver and quantification is shown. g Quantification of whole liver weight. The mean ± SEM is reported. The number of independent mice/group is indicated in the figure as individual data points. In a the secondary antibody–alone control is shown. Scale bars: 250 µm, and inset boxes: 50 µm. Statistical analyses regarding testing for the normality of data followed by appropriate statistical analyses were described in Materials and Methods. P- values were determined by unpaired T-test or Wilcoxon rank-sum test depending on if the data passed the Shapiro-Wilk normality test.

Article Snippet: Sections were incubated with propylene glycol for 2 min, then incubated with pre-heated Oil Red O staining solution (American MasterTech, STOROPT) at 60 °C for an additional 8 min.

Techniques: Immunofluorescence, Staining