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primary antibodies directed against mature neuronal marker neun  (Millipore)

 
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    Millipore primary antibodies directed against mature neuronal marker neun
    Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the <t>mature</t> <t>neuronal</t> marker <t>NeuN</t> with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.
    Primary Antibodies Directed Against Mature Neuronal Marker Neun, supplied by Millipore, 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/primary antibodies directed against mature neuronal marker neun/product/Millipore
    Average 90 stars, based on 1 article reviews
    primary antibodies directed against mature neuronal marker neun - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Selective Elimination of Corticogeniculate Feedback Abolishes the Electroencephalogram Dependence of Primary Visual Cortical Receptive Fields and Reduces Their Spatial Specificity"

    Article Title: Selective Elimination of Corticogeniculate Feedback Abolishes the Electroencephalogram Dependence of Primary Visual Cortical Receptive Fields and Reduces Their Spatial Specificity

    Journal: The Journal of Neuroscience

    doi: 10.1523/JNEUROSCI.23-18-07021.2003

    Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the mature neuronal marker NeuN with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.
    Figure Legend Snippet: Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the mature neuronal marker NeuN with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.

    Techniques Used: Labeling, Marker, Sampling



    Similar Products

    primary antibodies directed against mature neuronal marker neun  (Millipore)
    90
    Millipore primary antibodies directed against mature neuronal marker neun
    Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the <t>mature</t> <t>neuronal</t> marker <t>NeuN</t> with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.
    Primary Antibodies Directed Against Mature Neuronal Marker Neun, supplied by Millipore, 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/primary antibodies directed against mature neuronal marker neun/product/Millipore
    Average 90 stars, based on 1 article reviews
    primary antibodies directed against mature neuronal marker neun - by Bioz Stars, 2026-03
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the mature neuronal marker NeuN with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.

    Journal: The Journal of Neuroscience

    Article Title: Selective Elimination of Corticogeniculate Feedback Abolishes the Electroencephalogram Dependence of Primary Visual Cortical Receptive Fields and Reduces Their Spatial Specificity

    doi: 10.1523/JNEUROSCI.23-18-07021.2003

    Figure Lengend Snippet: Highly selective elimination of corticogeniculate neurons in areas 17-18 of experimental cortex. a, Gyrus lateralis of an experimental cat 14 d after induction of apoptosis. The red arrow indicates the center and direction of photoactivation by incident light (1.9 mm diameter region of photoactivation); L, lateral; V, ventral; WM, white matter. b, c, Merged overlay of images for the rhodamine fluorochrome carried by the targeting nanospheres (red) and immunocytochemical labeling for the mature neuronal marker NeuN with Cy2 (green). b, High magnification image of the blue-boxed region in a, demonstrating the highly efficient elimination of corticogeniculate projection neurons in the experimentally targeted region. c, High magnification image of the red-boxed region in a, demonstrating the normal appearance of corticogeniculate neurons in control primary visual cortex. d-f, Quantification of corticogeniculate neuron loss by relative cell density profiles. Regions denoted by gray and white shading represent assignment to specific cortical layers (noted above the abscissa). d, Density profile in regions of corticogeniculate neuron apoptosis at the tip of the gyrus and in the homologous regions in the control hemisphere (see insets above). e, Control region at the tip of the gyrus 3-6 mm anterior to the affected region, within the same experimental hemisphere (see inset). f, Control regions deep in the medial or lateral banks of the experimental hemisphere. Note that layer 5A is relatively thicker than layers 5B-6 in these deep regions compared with that at the tip of the gyrus, as indicated by three sampling windows and thicker area of gray shading. Error bars in d-f indicate SDs from the means.

    Article Snippet: Sections from the regions of targeted neuronal apoptosis and the homologous regions of the control hemispheres were processed for immunocytochemistry using primary antibodies directed against the mature neuronal marker NeuN (Chemicon, Temecula, CA).

    Techniques: Labeling, Marker, Sampling