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  • 94
    Millipore one m173 semithin sections
    One M173 Semithin Sections, supplied by Millipore, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Merck KGaA semithin sections
    A , light microscopy of <t>semithin</t> sections of Kir4.1 +/+ and Kir4.1 −/− stomach mucosae. In both genotypes, droplets of varying size can be observed in the cells directly lining the lumen, indicative of milk absorption. Some of the PCs in
    Semithin Sections, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 92/100, based on 39 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    Olympus semithin toluidine blue stained sections
    A , light microscopy of <t>semithin</t> sections of Kir4.1 +/+ and Kir4.1 −/− stomach mucosae. In both genotypes, droplets of varying size can be observed in the cells directly lining the lumen, indicative of milk absorption. Some of the PCs in
    Semithin Toluidine Blue Stained Sections, supplied by Olympus, used in various techniques. Bioz Stars score: 91/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    Carl Zeiss semithin sections semithin
    Lipid droplets in the Drosophila brain. (A-E) Pictures taken from third instar larval brains. (A) Oil Red O staining, note an intense staining in the dorso-medial part of the central brain. (B) Toluidine blue-stained <t>semithin</t> section from the brain cortex. LDs (green) are organized in large clusters between neurons. (C) Pseudocolored electron micrograph taken from the brain cortex. LDs (green) are found in the cytoplasm of glial cells (G, red) but not in neurons (N). (D) High power electron micrograph from the perinuclear region of a cortex glia (G) LDs are rounded electron-opaque structures, delineated by a phospholipid monolayer (inset, arrow). N: neuron. (E) LDs (brown) are generally found in the closest vicinity of neuroblasts (asterisks). Unstained semithin section. (F) Diagram representing the distribution of LDs between neurons and glial cells. (G) Number of LDs in order of their distance from neuroblasts. (H) Time-course changes in the amount of accumulated LDs per brain tissue area ratio. Standard deviations are indicated. Scalebars: (A) 100 μm (B) 10 μm (C) 1μm, (D) 500nm, inset: 200nm, (E) 10 μm.
    Semithin Sections Semithin, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 88/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Hamamatsu semithin sections
    Immuno-EM of Cx29. These are images of teased fibers that were fixed in 0.5% glutaraldehyde, immunostained for Cx29 using DAB as the substrate for peroxidase, and processed for EM. Two teased fibers are illustrated in A , unstained <t>semithin</t> sections are shown in B and C , and thin sections photographed with an electron microscope are shown in D and E . In all panels , there is DAB throughout incisures ( arrowheads ) and in the innermost aspects of the juxtaparanodal/paranodal regions ( arrows ) of myelinating Schwann cells. SC , Schwann cell nucleus; M , myelin sheath; A , axon. Double arrowheads , Node of Ranvier. Scale bars: A–C , 10 μm; D, E , 1 μm.
    Semithin Sections, supplied by Hamamatsu, used in various techniques. Bioz Stars score: 92/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    Heraeus Kulzer semithin sections
    Immuno-EM of Cx29. These are images of teased fibers that were fixed in 0.5% glutaraldehyde, immunostained for Cx29 using DAB as the substrate for peroxidase, and processed for EM. Two teased fibers are illustrated in A , unstained <t>semithin</t> sections are shown in B and C , and thin sections photographed with an electron microscope are shown in D and E . In all panels , there is DAB throughout incisures ( arrowheads ) and in the innermost aspects of the juxtaparanodal/paranodal regions ( arrows ) of myelinating Schwann cells. SC , Schwann cell nucleus; M , myelin sheath; A , axon. Double arrowheads , Node of Ranvier. Scale bars: A–C , 10 μm; D, E , 1 μm.
    Semithin Sections, supplied by Heraeus Kulzer, used in various techniques. Bioz Stars score: 92/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore semithin sections
    Immuno-EM of Cx29. These are images of teased fibers that were fixed in 0.5% glutaraldehyde, immunostained for Cx29 using DAB as the substrate for peroxidase, and processed for EM. Two teased fibers are illustrated in A , unstained <t>semithin</t> sections are shown in B and C , and thin sections photographed with an electron microscope are shown in D and E . In all panels , there is DAB throughout incisures ( arrowheads ) and in the innermost aspects of the juxtaparanodal/paranodal regions ( arrows ) of myelinating Schwann cells. SC , Schwann cell nucleus; M , myelin sheath; A , axon. Double arrowheads , Node of Ranvier. Scale bars: A–C , 10 μm; D, E , 1 μm.
    Semithin Sections, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 293 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    A , light microscopy of semithin sections of Kir4.1 +/+ and Kir4.1 −/− stomach mucosae. In both genotypes, droplets of varying size can be observed in the cells directly lining the lumen, indicative of milk absorption. Some of the PCs in

    Journal: The Journal of Biological Chemistry

    Article Title: Kir4.1 Channel Expression Is Essential for Parietal Cell Control of Acid Secretion *

    doi: 10.1074/jbc.M110.151191

    Figure Lengend Snippet: A , light microscopy of semithin sections of Kir4.1 +/+ and Kir4.1 −/− stomach mucosae. In both genotypes, droplets of varying size can be observed in the cells directly lining the lumen, indicative of milk absorption. Some of the PCs in

    Article Snippet: Semithin sections (1 μm) of these samples were collected on glass slides pretreated with 3-(triethoxysilyl)propylamide (silane; Merck, Darmstadt, Germany).

    Techniques: Light Microscopy

    Lipid droplets in the Drosophila brain. (A-E) Pictures taken from third instar larval brains. (A) Oil Red O staining, note an intense staining in the dorso-medial part of the central brain. (B) Toluidine blue-stained semithin section from the brain cortex. LDs (green) are organized in large clusters between neurons. (C) Pseudocolored electron micrograph taken from the brain cortex. LDs (green) are found in the cytoplasm of glial cells (G, red) but not in neurons (N). (D) High power electron micrograph from the perinuclear region of a cortex glia (G) LDs are rounded electron-opaque structures, delineated by a phospholipid monolayer (inset, arrow). N: neuron. (E) LDs (brown) are generally found in the closest vicinity of neuroblasts (asterisks). Unstained semithin section. (F) Diagram representing the distribution of LDs between neurons and glial cells. (G) Number of LDs in order of their distance from neuroblasts. (H) Time-course changes in the amount of accumulated LDs per brain tissue area ratio. Standard deviations are indicated. Scalebars: (A) 100 μm (B) 10 μm (C) 1μm, (D) 500nm, inset: 200nm, (E) 10 μm.

    Journal: PLoS ONE

    Article Title: Specialized Cortex Glial Cells Accumulate Lipid Droplets in Drosophila melanogaster

    doi: 10.1371/journal.pone.0131250

    Figure Lengend Snippet: Lipid droplets in the Drosophila brain. (A-E) Pictures taken from third instar larval brains. (A) Oil Red O staining, note an intense staining in the dorso-medial part of the central brain. (B) Toluidine blue-stained semithin section from the brain cortex. LDs (green) are organized in large clusters between neurons. (C) Pseudocolored electron micrograph taken from the brain cortex. LDs (green) are found in the cytoplasm of glial cells (G, red) but not in neurons (N). (D) High power electron micrograph from the perinuclear region of a cortex glia (G) LDs are rounded electron-opaque structures, delineated by a phospholipid monolayer (inset, arrow). N: neuron. (E) LDs (brown) are generally found in the closest vicinity of neuroblasts (asterisks). Unstained semithin section. (F) Diagram representing the distribution of LDs between neurons and glial cells. (G) Number of LDs in order of their distance from neuroblasts. (H) Time-course changes in the amount of accumulated LDs per brain tissue area ratio. Standard deviations are indicated. Scalebars: (A) 100 μm (B) 10 μm (C) 1μm, (D) 500nm, inset: 200nm, (E) 10 μm.

    Article Snippet: Semithin sections Semithin (0,5 μm) sections from Durcupan embedded blocks were cut with glass knives stained in 1% toluidine blue– 1% azure II solution mounted in pure glycerol and viewed in a Zeiss AxioImager Z1 microscope with a 63x oil immersion objective, using an ICc1 camera.

    Techniques: Staining

    Immuno-EM of Cx29. These are images of teased fibers that were fixed in 0.5% glutaraldehyde, immunostained for Cx29 using DAB as the substrate for peroxidase, and processed for EM. Two teased fibers are illustrated in A , unstained semithin sections are shown in B and C , and thin sections photographed with an electron microscope are shown in D and E . In all panels , there is DAB throughout incisures ( arrowheads ) and in the innermost aspects of the juxtaparanodal/paranodal regions ( arrows ) of myelinating Schwann cells. SC , Schwann cell nucleus; M , myelin sheath; A , axon. Double arrowheads , Node of Ranvier. Scale bars: A–C , 10 μm; D, E , 1 μm.

    Journal: The Journal of Neuroscience

    Article Title: Connexin29 Is Uniquely Distributed within Myelinating Glial Cells of the Central and Peripheral Nervous Systems

    doi: 10.1523/JNEUROSCI.22-15-06458.2002

    Figure Lengend Snippet: Immuno-EM of Cx29. These are images of teased fibers that were fixed in 0.5% glutaraldehyde, immunostained for Cx29 using DAB as the substrate for peroxidase, and processed for EM. Two teased fibers are illustrated in A , unstained semithin sections are shown in B and C , and thin sections photographed with an electron microscope are shown in D and E . In all panels , there is DAB throughout incisures ( arrowheads ) and in the innermost aspects of the juxtaparanodal/paranodal regions ( arrows ) of myelinating Schwann cells. SC , Schwann cell nucleus; M , myelin sheath; A , axon. Double arrowheads , Node of Ranvier. Scale bars: A–C , 10 μm; D, E , 1 μm.

    Article Snippet: Light microscopic images of the teased fibers and semithin sections were generated with a cooled Hamamatsu camera.

    Techniques: Microscopy