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rat anti myelin basic protein  (Novus Biologicals)


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    Novus Biologicals rat anti myelin basic protein
    Rat Anti Myelin Basic Protein, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 95/100, based on 46 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+anti+mbp/pm41932622-128-54-61?v=Novus+Biologicals
    Average 95 stars, based on 46 article reviews
    rat anti myelin basic protein - by Bioz Stars, 2026-08
    95/100 stars

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    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked <t>by</t> <t>CNP</t> immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of <t>MBP</t> and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.
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    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked <t>by</t> <t>CNP</t> immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of <t>MBP</t> and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.
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    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked <t>by</t> <t>CNP</t> immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of <t>MBP</t> and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.
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    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked <t>by</t> <t>CNP</t> immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of <t>MBP</t> and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.
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    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked <t>by</t> <t>CNP</t> immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of <t>MBP</t> and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.
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    (A) Optic nerve sections were immunostained with an <t>anti-MBP</t> antibody (green). Representative confocal images from 7-month-old WT (top) and Wfs1 KO (bottom) mice are shown along with the corresponding high-magnification zoom of the boxed area. Scale bar, 50 µm. Quantification of MBP fluorescence mean intensity in optic nerve sections from (B) 4-month (C) 7-month old animals. Data are presented as normalized values ± SEM relative to the WT mean. Statistical analysis was performed using a two-tailed unpaired Student’s I-test with Welch’s correction. n≥ 5. ns - not significant.
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    (A) Optic nerve sections were immunostained with an <t>anti-MBP</t> antibody (green). Representative confocal images from 7-month-old WT (top) and Wfs1 KO (bottom) mice are shown along with the corresponding high-magnification zoom of the boxed area. Scale bar, 50 µm. Quantification of MBP fluorescence mean intensity in optic nerve sections from (B) 4-month (C) 7-month old animals. Data are presented as normalized values ± SEM relative to the WT mean. Statistical analysis was performed using a two-tailed unpaired Student’s I-test with Welch’s correction. n≥ 5. ns - not significant.
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    (A) Optic nerve sections were immunostained with an <t>anti-MBP</t> antibody (green). Representative confocal images from 7-month-old WT (top) and Wfs1 KO (bottom) mice are shown along with the corresponding high-magnification zoom of the boxed area. Scale bar, 50 µm. Quantification of MBP fluorescence mean intensity in optic nerve sections from (B) 4-month (C) 7-month old animals. Data are presented as normalized values ± SEM relative to the WT mean. Statistical analysis was performed using a two-tailed unpaired Student’s I-test with Welch’s correction. n≥ 5. ns - not significant.
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    Image Search Results


    Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked by CNP immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of MBP and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.

    Journal: bioRxiv

    Article Title: Red fluorescent labeling of myelin by membrane-targeted tdTomato in transgenic mouse lines

    doi: 10.64898/2026.04.17.718425

    Figure Lengend Snippet: Upper panels: Fluorescence micrographs visualizing that transgenically expressed tdTomato is localized in the processes and somata of oligodendrocytes which are marked by CNP immunolabeling. A fraction of CNP-positive oligodendrocytes does not express tdTomato (purple arrows), corresponding to the expression pattern as described in . Lower panels: Colocalization of MBP and tdTomato in myelin. The fluorescence signal is observed on both sides of the axon, while the enwrapped axon shows no fluorescence (white arrow in the inset). The cyan arrows highlight primary processes of oligodendrocytes connecting soma and myelin sheaths, which are labeled by tdTomato, but not stained for MBP. CB: cerebellum; CTX: cortex; HIP: hippocampus. The letters in the circles indicate the CNPMTO mouse line. Scale bar: 10 µm. Scale bar inset: 4 µm.

    Article Snippet: Free-floating slices were permeabilized in 0.4% Triton X-100/PBS for 30 min and blocked with 4% fetal calf serum (FCS) in 0.2% Triton X-100/PBS for 1 h. Sections were immunohistochemically stained either for MBP (rat anti-MBP, AbD Serotec #MCA409S) or CNP (guinea pig anti-CNP, Synaptic Systems #355004).

    Techniques: Fluorescence, Immunolabeling, Expressing, Labeling, Staining

    (A) Optic nerve sections were immunostained with an anti-MBP antibody (green). Representative confocal images from 7-month-old WT (top) and Wfs1 KO (bottom) mice are shown along with the corresponding high-magnification zoom of the boxed area. Scale bar, 50 µm. Quantification of MBP fluorescence mean intensity in optic nerve sections from (B) 4-month (C) 7-month old animals. Data are presented as normalized values ± SEM relative to the WT mean. Statistical analysis was performed using a two-tailed unpaired Student’s I-test with Welch’s correction. n≥ 5. ns - not significant.

    Journal: bioRxiv

    Article Title: Synaptic Alterations Are Preceding the Axonal Loss in Optic Atrophy of Wolfram Syndrome Mouse Model

    doi: 10.64898/2026.03.22.713521

    Figure Lengend Snippet: (A) Optic nerve sections were immunostained with an anti-MBP antibody (green). Representative confocal images from 7-month-old WT (top) and Wfs1 KO (bottom) mice are shown along with the corresponding high-magnification zoom of the boxed area. Scale bar, 50 µm. Quantification of MBP fluorescence mean intensity in optic nerve sections from (B) 4-month (C) 7-month old animals. Data are presented as normalized values ± SEM relative to the WT mean. Statistical analysis was performed using a two-tailed unpaired Student’s I-test with Welch’s correction. n≥ 5. ns - not significant.

    Article Snippet: Primary antibodies against Brn3a (MAB1585, Millipore, 1:250), RBPMS (GTX118619, GeneTex, 1:200), NF200 (N4142, Sigma-Aldrich, 1:2000), GFAP (PA1-10004, Invitrogen, 1:2000), MBP aa82–87 (MCA409S, Bio-Rad, 1:50), β-III Tubulin (ab18207, Abcam, 1:750), PSD95 (51-6900, Invitrogen, 1:150), and Synaptophysin (101 004, Synaptic Systems, 1:2000) were applied overnight at 4°C.

    Techniques: Fluorescence, Two Tailed Test