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guinea pig polyclonal anti mor  (Millipore)


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    Millipore guinea pig polyclonal anti mor
    Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit <t>polyclonal</t> antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).
    Guinea Pig Polyclonal Anti Mor, 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/guinea pig polyclonal anti mor/product/Millipore
    Average 90 stars, based on 1 article reviews
    guinea pig polyclonal anti mor - by Bioz Stars, 2026-06
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    Images

    1) Product Images from "Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice"

    Article Title: Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice

    Journal: Frontiers in Molecular Neuroscience

    doi: 10.3389/fnmol.2023.1139118

    Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit polyclonal antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).
    Figure Legend Snippet: Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit polyclonal antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).

    Techniques Used: Over Expression, Modification, Expressing, Immunostaining, Marker, Generated, Staining, Labeling



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    Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit <t>polyclonal</t> antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).
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    Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit <t>polyclonal</t> antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).
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    Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit polyclonal antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).

    Journal: Frontiers in Molecular Neuroscience

    Article Title: Excessive self-grooming, gene dysregulation and imbalance between the striosome and matrix compartments in the striatum of Shank3 mutant mice

    doi: 10.3389/fnmol.2023.1139118

    Figure Lengend Snippet: Altered transcriptome of D1- and D2-MSN, over-expression of GAD65, and modification of the striosome/matrix balance in the striatum of Shank3 Δ11/Δ11 mice. (A) Enrichment of RNAseq DEGs in the striatum of Shank3 Δ11/Δ11 mice compared to cell-specific gene clusters suggested by and . Genes under-expressed in Shank3 Δ11/Δ11 striatum are enriched in D1-MSN clusters while genes over-expressed in Shank3 Δ11/Δ11 striatum are enriched in D2-MSN clusters. Ratio genes correspond to the proportion of DEGs enriched in the cluster. Over-representation analyses were performed with Fisher’s hypergeometric tests and p -values were adjusted for multiple testing with the Benjamini–Hochberg procedure within each category of DEGs. (B) Comparison of the log of the fold change of gene expression of selected genes in Shank3 Δ11/Δ11 vs. Shank3 +/+ mice (LogFC RNAseq, Y axis) and the β values (slope of the linear regression) for low self-grooming vs. high self-grooming ( β value grooming, X axis). (C,D) Confocal images of striatum coronal sections of one-year old Shank3 +/+ male mice. (C) GAD65 immunoreactivity (red) is enriched in striatal microzones identified as striosomes by immunostaining for μ-opioid receptor (MOR, in green), a canonical marker of striosomes. (D) Increased GAD65 immunoreactivity in striosomes (arrows) and subcallosal streak (two-headed arrows) compared to surrounding matrix is observed with two different antibodies: the rabbit polyclonal antibody (Invitrogen PA5-77983 in red) used in (C,E,F) and a mouse monoclonal antibody (Millipore MAB351, in green). (E,F) Distribution and quantification of GAD65 immunoreactivity in dorsal striatum sections of a Shank3 +/+ (E) and a Shank3 Δ11/Δ11 (F) mouse (images generated by stitching multiple maximum-intensity projected z-stacks). The arrows point to striosomes and the arrowheads to subcallosal streak. In the dorsal striatum ROI (surrounded in green), the unlabeled myelinated fibers are colored in red, the regions of higher expression of GAD65 (striosomes) are colored in green, and the regions of lower expression of GAD65 (matrix) are uncolored. The cortex ROI used as a reference is surrounded in red. Note that the acquisition parameters were adjusted for each brain hemi-section in order to have no saturating signal for GAD65 in the striatal ROI. Increased intensity in the striatum thus leads to a staining which appears weaker in the cortex. (G–I) Comparison of GAD65 immunoreactivity in the striosome and matrix compartments of the dorsal striatum in 5 Shank3 +/+ (green) and 9 Shank3 Δ11/Δ11 (orange) 1-year old male mice. (G) Relative surface of the GAD65-enriched striosome compartment (surface of striosomes/surface of (striosomes + matrix). (H) Relative GAD65 labeling intensity in the striosomal compartment of the striatum compared to cortex. (I) Relative GAD65 labeling intensity in the matrix compartment of the striatum compared to cortex. Data, generated from analysis of 9–14 images per animal, are presented as box-plots (median, first, and third quartiles).

    Article Snippet: The free-floating sections were rinsed three times in PBS (pH 7.4) and then incubated in NH4Cl (Sigma-Aldrich) 50 mM in PBS for 15 min. After three PBS washes (5 min each), sections were incubated for 1 h at room temperature in PBS containing 1% bovine serum albumin (Applichem) and 0.3% Triton X-100 (Sigma-Aldrich) (PBS/BSA/TX) before incubation for ≈ 20 h at room temperature with the following primary antibodies diluted in PBS/BSA/TX: rabbit polyclonal anti-GAD65 (Invitrogen PA5-77983, 1/200), mouse monoclonal anti-GAD65 (Millipore MAB351, 1/500), guinea pig polyclonal anti MOR (Millipore AB5509, 1/100), rabbit polyclonal anti-VGLUT1 (Synaptic Systems 135303, 1/1000), and mouse monoclonal anti-SHANK3 (Santa Cruz Biotechnology sc-377088, 1/1000).

    Techniques: Over Expression, Modification, Expressing, Immunostaining, Marker, Generated, Staining, Labeling