statistical parametric mapping version 12 software package Search Results


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Revvity ivis lumina
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
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Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
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MathWorks Inc spm12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Spm12, supplied by MathWorks Inc, 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/spm12/product/MathWorks Inc
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MathWorks Inc statistical parametric mapping (spm) 12 software, version 7219
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Statistical Parametric Mapping (Spm) 12 Software, Version 7219, supplied by MathWorks Inc, 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/statistical parametric mapping (spm) 12 software, version 7219/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
statistical parametric mapping (spm) 12 software, version 7219 - by Bioz Stars, 2026-03
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90
MathWorks Inc statistical parametric mapping version 12 (spm12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Statistical Parametric Mapping Version 12 (Spm12, supplied by MathWorks 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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MathWorks Inc statistical parametric mapping software 12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Statistical Parametric Mapping Software 12, supplied by MathWorks Inc, 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/statistical parametric mapping software 12/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
statistical parametric mapping software 12 - by Bioz Stars, 2026-03
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Cell Signaling Technology Inc erk antibody
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
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Cordis corporation carto electroanatomical mapping
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
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MapleSoft Inc maple 12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Maple 12, supplied by MapleSoft Inc, 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/maple 12/product/MapleSoft Inc
Average 90 stars, based on 1 article reviews
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MathWorks Inc statistical parametric mapping (spm) version 12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Statistical Parametric Mapping (Spm) Version 12, supplied by MathWorks Inc, 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/statistical parametric mapping (spm) version 12/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
statistical parametric mapping (spm) version 12 - by Bioz Stars, 2026-03
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MapleSoft Inc maple 12 software
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Maple 12 Software, supplied by MapleSoft 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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MathWorks Inc statistical parametric mapping 12
Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and <t>IVIS</t> imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.
Statistical Parametric Mapping 12, supplied by MathWorks Inc, 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/result/statistical parametric mapping 12/product/MathWorks Inc
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Image Search Results


Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and IVIS imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.

Journal: bioRxiv

Article Title: Designer Fat Cells: Adipogenic Differentiation of CRISPR-Cas9 Genome-Engineered Induced Pluripotent Stem Cells

doi: 10.1101/2023.10.26.564206

Figure Lengend Snippet: Different cell concentrations of Ccl2-Luciferase PDiPSCs primed in adipogenic media for 3 days were injected into LD mice and IVIS imaging was used to quantify cells present in the mouse, (a) Photon flux per animal was calculated every week for 4 weeks. Bars represent mean photon flux + SEM (n=3- 7). Exact p values are displayed using LD mice with PBS injection as the control, (b) WT and LD mice were injected with 20e 6 cells and imaged for 28 weeks using IVIS imaging. Values represent mean photon flux ± SEM (n=3-7). All statistics were run using a 2-way ANOVA with Sidak’s post-hoc test. SEM, standard error of the mean, (c) Representative images of WT and LD mice at various timepoints from IVIS imaging are shown. The red circle highlights the area of injection.

Article Snippet: After waiting 10 minutes, mice were positioned on their dorsal aspect and images were taken from the ventral view with an exposure time of 5 minutes using an IVIS Lumina (PerkinElmer, Waltham, MA, USA; Living Image 4.2; 1-min exposure; bin, 8; field of view, 12.5 cm; f/stop, 1; open filter).

Techniques: Luciferase, Injection, Imaging, Control