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anti p2y12 receptor extracellular pe antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs anti p2y12 receptor extracellular pe antibody
    Anti P2y12 Receptor Extracellular Pe Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/p2y12/Anti-P2Y12+Receptor+(extracellular)-PE+Antibody/pm41980755-59-32-37
    Average 94 stars, based on 3 article reviews
    anti p2y12 receptor extracellular pe antibody - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    other:

    Article Title: Combination therapy with Treg and MSC enhances potency and attenuation of inflammation after traumatic brain injury compared to monotherapy
    Article Snippet: FITC , P2Y12 , n/a , Alomone Labs.

    Blocking Assay:

    Article Title: Analysis of purine receptor expression and functionality in alveolar epithelial cells.
    Article Snippet: The samples were separated by a 4–12% Bis-Tris polyacrylamide gel (NuPage, Life Technologies GmbH) and transferred to nitrocellulose filters (Life Technologies GmbH) by electroblotting. .. After addition of blocking buffer (PBS plus 0.1% Tween containing 5% milk powder) followed by agitation for 1 h, specific P2R antibodies were applied overnight at 4 °C (P2Y2, P2Y4, P2Y6, P2Y12, P2Y13, P2X3, P2X4, P2X5, and P2X7 from Alomone Labs, Jerusalem, Israel; P2Y1 from Genway, San Diego, CA, USA; and P2Y14 from Abcam, Cambridge, UK). .. Bound primary antibodies were visualized using horseradish peroxidase-conjugated secondary antibodies (1 h at room temperature with agitation) and enhanced chemiluminescent substrate (ECL) reagent (ECL Plus Western Blotting Detection Reagents, GE Healthcare, Freiburg, Germany) according to the manufacturer’s protocol.

    Incubation:

    Article Title: Study of the Involvement of the P2Y12 Receptor in Chronic Itching in Type 2 Diabetes Mellitus.
    Article Snippet: Itching is a common clinical symptom in diabetic patients.. This research is to carry out experiments on the pathological changes in the P2Y12 receptor in type 2 diabetes mellitus complicated with chronic itching.. Changes in body weight, fasting blood glucose (FBG), thermal hyperalgesia, cold hyperalgesia, spontaneous itching, and sciatic nerve conduction velocity were detected.

    Article Title: Implication of P2Y 12 receptor in uc.48+-mediated abnormal sympathoexcitatory reflex via superior cervical ganglia in myocardial ischemic rats.
    Article Snippet: Purinergic 2Y12 (P2Y12) receptor antagonists are used as platelet aggregation inhibitors.. Long non-coding RNAs (lncRNAs) play an important role in neuropathological events.. Satellite glial cells (SGCs) in the superior cervical ganglia (SCGs) encircle the somata of neurons.

    Chemotaxis Assay:

    Article Title: Human cord blood‐derived regulatory T ‐cell therapy modulates the central and peripheral immune response after traumatic brain injury
    Article Snippet: .. BV421 , P2Y12 , n/a , Alomone Labs , APR‐020‐F , Mediates microglia chemotaxis. ..



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    Alomone Labs anti p2y12 receptor extracellular pe antibody
    Anti P2y12 Receptor Extracellular Pe Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/p2y12/Anti-P2Y12+Receptor+(extracellular)-PE+Antibody/pm41980755-59-32-37
    Average 94 stars, based on 1 article reviews
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    Oxford Instruments microglial cells p2y12
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Accumetrics verifynow p2y12 analyzer
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Oxford Instruments imaris
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Accriva Inc verifynow p2y12
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Alomone Labs anti p2y12 receptor antibody
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
    Anti P2y12 Receptor Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Genechem shrna plasmid targeting p2y12
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
    Shrna Plasmid Targeting P2y12, supplied by Genechem, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs anti p2y12r antibody
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Alomone Labs anti p2y 12 antibody
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
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    Alomone Labs anti p2y12 antibody
    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia <t>(P2Y12</t> + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .
    Anti P2y12 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia (P2Y12 + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .

    Journal: EMBO Molecular Medicine

    Article Title: Blocking microglial reactivity via purinergic receptors prevents subacute cognitive deficits after TIA

    doi: 10.1038/s44321-026-00397-6

    Figure Lengend Snippet: ( A ) Representative scheme of the microperfusion system. ( B ) Heat map of all ANOVA+ proteins of the LC-MS analysis of the perfusate products, ( C ) protein intensity over time, top ten upregulated genes and pathway analysis from cluster 3 and ( D ) cluster 5 in males ( n = 5 per group). ( E ) Uniform manifold approximation and projection (UMAP) plot, colored by identified clusters (different cell types). ( F ) Number of differentially expressed genes ( p < 0.05) at 24 h and 3 d after TIA in each cell type compared to control (naïve) in males ( n = 3 per group). ( G ) Volcano plot of differentially regulated genes in microglia 3 d compared to naïve animals. Cut-off for illustrating gene names: Log2FC >|2| illustrated by vertical gray dashed lines, adjusted p value: >−log10(0.05) illustrated by horizontal gray dashed line ( n = 3 per group). ( H ) Representative image and quantification of microglia (P2Y12R + ) and neuron soma (KV2.1 + ) contacts 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 20 µm. ( I ) Representative image of microglia (P2Y12 + ) and synapse (Vglut + Homer + ) staining for synapse engulfed quantification 24 h after TIA in males ( n = 5 per group; p value = 0.0079), scale bar = 1 µm. Statistical tests: ( B – D ) Two-way ANOVA, Fisher’s exact testing. ( G ) Wilcoxon rank sum test + Bonferroni correction. ( H , I ) Two-way Student’s t -test. Error bars indicate ±SD. * p < 0.05. .

    Article Snippet: For the microglia-synapse analysis, confocal Z-stack images were processed, and colocalizations of synapses (VGlut+ Homer+) in contact with microglial cells (P2Y12+) were analyzed using Imaris software.

    Techniques: Liquid Chromatography with Mass Spectroscopy, Control, Staining

    ( A ) Luciferace assay to detect ATP concentration from peri-lesional perfusate (see Fig. ) at before (BL) and at indicated time points after TIA in males ( n = 6 per group; 10 min: p value = 0.0002, 24 h: p value = 0.0231). ( B ) Quantification of extracellular ATP (hsyn-cATPs) using in vivo two-photon imaging before (BL) and at indicated time points after TIA ( n = 18 per group; 10 min: p value <0.01) and ( C ) microglial processes (Cx3Cr1cre-TdTomato) recruitment to focal increase in extracellular ATP within 3 min after TIA in males. ( D ) Representative image of Iba1+ microglia cell and 3D reconstructed microglia for branches nodes analysis 24 h after cisterna magna injection of different ATP concentrations in males ( n = 6 per group; 0.3, 1, and 3 µg ATP: p value <0.0001), scale bar = 20 µm. ( E ) Quantification of colocalized presynaptic and postsynaptic particles 24 h after cisterna magna injection of different ATP concentrations in males ( n = 6 per group; 0.3, 1, and 3 µg ATP: p value <0.0001). ( F ) Microglia sphericity ( n = 5 per group; Veh: p value <0.0001 and P2Y12Ri: p value <0.0001), ( G ) synapse (Vglut + Homer + ) contacts with microglial cells (P2Y12 + ) ( n = 10 per group; Veh: p value <0.0033 and P2Y12Ri: p value <0.0035) (scale bar = 2 µm) and ( H ) glutamatergic synapse counts ( n = 5 per group) in sham and 24 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals (in males’ mice); Veh: p value = 0.0140 and P2Y12Ri: p value = 0.0155. ( I ) Neuroscore at 48 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals ( n = 10 per group; p value = 0.0002) and ( J ) Barnes Maze test ( n = 10 per group) in Sham and 48 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals (in males’ mice); Veh: p value = 0.0083 and P2Y12Ri: p value = 0.0469. Statistical tests: ( A – J ) two-way ANOVA, corrected for multiple comparisons using two-stage step-up method of Benjamin Kriegel. (I) Mann–Whitney U -test. Error bars indicate ±SD. * p < 0.05. .

    Journal: EMBO Molecular Medicine

    Article Title: Blocking microglial reactivity via purinergic receptors prevents subacute cognitive deficits after TIA

    doi: 10.1038/s44321-026-00397-6

    Figure Lengend Snippet: ( A ) Luciferace assay to detect ATP concentration from peri-lesional perfusate (see Fig. ) at before (BL) and at indicated time points after TIA in males ( n = 6 per group; 10 min: p value = 0.0002, 24 h: p value = 0.0231). ( B ) Quantification of extracellular ATP (hsyn-cATPs) using in vivo two-photon imaging before (BL) and at indicated time points after TIA ( n = 18 per group; 10 min: p value <0.01) and ( C ) microglial processes (Cx3Cr1cre-TdTomato) recruitment to focal increase in extracellular ATP within 3 min after TIA in males. ( D ) Representative image of Iba1+ microglia cell and 3D reconstructed microglia for branches nodes analysis 24 h after cisterna magna injection of different ATP concentrations in males ( n = 6 per group; 0.3, 1, and 3 µg ATP: p value <0.0001), scale bar = 20 µm. ( E ) Quantification of colocalized presynaptic and postsynaptic particles 24 h after cisterna magna injection of different ATP concentrations in males ( n = 6 per group; 0.3, 1, and 3 µg ATP: p value <0.0001). ( F ) Microglia sphericity ( n = 5 per group; Veh: p value <0.0001 and P2Y12Ri: p value <0.0001), ( G ) synapse (Vglut + Homer + ) contacts with microglial cells (P2Y12 + ) ( n = 10 per group; Veh: p value <0.0033 and P2Y12Ri: p value <0.0035) (scale bar = 2 µm) and ( H ) glutamatergic synapse counts ( n = 5 per group) in sham and 24 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals (in males’ mice); Veh: p value = 0.0140 and P2Y12Ri: p value = 0.0155. ( I ) Neuroscore at 48 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals ( n = 10 per group; p value = 0.0002) and ( J ) Barnes Maze test ( n = 10 per group) in Sham and 48 h after TIA in vehicle (Veh) or P2Y12Ri (-inhibitor) treated animals (in males’ mice); Veh: p value = 0.0083 and P2Y12Ri: p value = 0.0469. Statistical tests: ( A – J ) two-way ANOVA, corrected for multiple comparisons using two-stage step-up method of Benjamin Kriegel. (I) Mann–Whitney U -test. Error bars indicate ±SD. * p < 0.05. .

    Article Snippet: For the microglia-synapse analysis, confocal Z-stack images were processed, and colocalizations of synapses (VGlut+ Homer+) in contact with microglial cells (P2Y12+) were analyzed using Imaris software.

    Techniques: Concentration Assay, In Vivo, Imaging, Injection, MANN-WHITNEY