small animal in vivo fluorescence imaging system Search Results


fluorescence imager for small animals ivis  (Caliper Life Sciences)
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Caliper Life Sciences fluorescence imager for small animals ivis
Fluorescence Imager For Small Animals Ivis, supplied by Caliper Life Sciences, 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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small animal near infrared fluorescence imager  (Siemens Healthineers)
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Siemens Healthineers small animal near infrared fluorescence imager
Small Animal Near Infrared Fluorescence Imager, supplied by Siemens Healthineers, 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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small animal fluorescence imaging system in-vivo imaging system fx pro  (Carestream Health)
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Carestream Health small animal fluorescence imaging system in-vivo imaging system fx pro
Small Animal Fluorescence Imaging System In Vivo Imaging System Fx Pro, supplied by Carestream Health, 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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small animal ccd-based fluorescence imager  (Caliper Life Sciences)
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Caliper Life Sciences small animal ccd-based fluorescence imager
Small Animal Ccd Based Fluorescence Imager, supplied by Caliper Life Sciences, 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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small animal living fluorescence imaging system xtrem  (Bruker Corporation)
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Bruker Corporation small animal living fluorescence imaging system xtrem
Small Animal Living Fluorescence Imaging System Xtrem, supplied by Bruker Corporation, 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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small animal ccd-based fluorescence imager ivis  (Caliper Life Sciences)
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Caliper Life Sciences small animal ccd-based fluorescence imager ivis
Small Animal Ccd Based Fluorescence Imager Ivis, supplied by Caliper Life Sciences, 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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whole-body multichannel small animal fluorescence reflectance imager in vivo fx pro  (Bruker Corporation)
90
Bruker Corporation whole-body multichannel small animal fluorescence reflectance imager in vivo fx pro
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
Whole Body Multichannel Small Animal Fluorescence Reflectance Imager In Vivo Fx Pro, supplied by Bruker Corporation, 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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near-infrared fluorescence imaging system for small animals in vivo  (Caliper Life Sciences)
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Caliper Life Sciences near-infrared fluorescence imaging system for small animals in vivo
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
Near Infrared Fluorescence Imaging System For Small Animals In Vivo, supplied by Caliper Life Sciences, 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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near-infrared fluorescence imaging system for small animals in vivo - by Bioz Stars, 2026-02
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ami small animal fluorescence imaging system  (Spectral Instruments Imaging)
90
Spectral Instruments Imaging ami small animal fluorescence imaging system
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
Ami Small Animal Fluorescence Imaging System, supplied by Spectral Instruments Imaging, 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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fluorescence small animal imager photon imager  (BIOSPACE LAB)
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BIOSPACE LAB fluorescence small animal imager photon imager
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
Fluorescence Small Animal Imager Photon Imager, supplied by BIOSPACE LAB, 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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in vivo animal fluorescence imager carestream health  (Carestream Health)
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Carestream Health in vivo animal fluorescence imager carestream health
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
In Vivo Animal Fluorescence Imager Carestream Health, supplied by Carestream Health, 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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deepvision nir-ii in vivo imaging system  (Nirmidas Biotech)
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Nirmidas Biotech deepvision nir-ii in vivo imaging system
Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by <t>fluorescence</t> <t>reflectance</t> imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.
Deepvision Nir Ii In Vivo Imaging System, supplied by Nirmidas Biotech, 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


Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by fluorescence reflectance imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.

Journal: Cellular and Molecular Gastroenterology and Hepatology

Article Title: Granulocyte Macrophage Colony-Stimulating Factor–Activated CD39 + /CD73 + Murine Monocytes Modulate Intestinal Inflammation via Induction of Regulatory T Cells

doi: 10.1016/j.jcmgh.2015.04.005

Figure Lengend Snippet: Granulocyte-macrophage colony-stimulating factor–activated monocytes (GMaM) infiltrate the intestine at higher numbers and persist longer. ( A ) GMaM and control monocytes were stained for cell surface expression of gut homing molecules and analyzed by flow cytometry. Expression is shown as representative dot plots gated on CD11b + cells showing Ly6c expression ( y axis) versus respective cell surface molecules ( x axis). ( B ) GMaM and control monocytes were labeled with 1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide and injected intravenously at day 13 of chronic dextran sulfate sodium–induced colitis. Monocyte infiltration in the intestine was visualized after 48 hours and 96 hours, and representative pictures are shown (n = 3). ( C ) After 96 hours, the intestine was removed and monocyte infiltration especially into Peyer’s patches, visualized by fluorescence reflectance imaging, was evaluated (arrow shows Peyer’s patches). ( D ) Mean fluorescence intensity (mean ± SEM) of Peyer’s patches is shown (n = 5–7). Statistical significance was determined by unpaired Student t -test. * P < .05.

Article Snippet: Ex vivo optical imaging of the dissected intestine placed on a petri dish 96 hours after intravenous injection was performed using a whole-body multichannel small animal fluorescence reflectance imager (in vivo FX Pro; Bruker, Billerica, MA).

Techniques: Control, Staining, Expressing, Flow Cytometry, Labeling, Injection, Fluorescence, Imaging