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rabbit polyclonal anti psd95 specific antibody  (Proteintech)

 
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    Structured Review

    Proteintech rabbit polyclonal anti psd95 specific antibody
    Reagents and instruments used in the study
    Rabbit Polyclonal Anti Psd95 Specific Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti psd95 specific antibody/product/Proteintech
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal anti psd95 specific antibody - by Bioz Stars, 2025-02
    86/100 stars

    Images

    1) Product Images from "Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2"

    Article Title: Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2

    Journal: Neural Regeneration Research

    doi: 10.4103/NRR.NRR-D-23-01051

    Reagents and instruments used in the study
    Figure Legend Snippet: Reagents and instruments used in the study

    Techniques Used: CCK-8 Assay, Saline, TUNEL Assay, DNA Extraction, Modification, Marker, Fluorescence, Microscopy, Imaging

    Treatment with NaHS inhibits the dysregulation of neuroplasticity induced by Quin. (A, B) Immunofluorescence images showing colocalization of PSD95 (red, CoraLite594 fluorescent dye) and NeuN (green, CoraLite488 fluorescent dye) in nine coronal sections from three mice per group. PSD95 expression was significantly upregulated in neuronal cells in the Quin + NaHS group compared with the Quin group, and this effect was reversed by the addition of ML385. Scale bar: 20 μm. (C) Western blot was used to measure PSD95, SYT1, and Syn expression levels 6 days after Quin striatal injection. Quantification of PSD95, SYT1, and Syn expression levels ( n = 3 per group). The values are reported as mean ± SD. *** P < 0.001 (one-way analysis of variance followed by Bonferroni post hoc test). NeuN: Neuronal nuclei; PSD95: postsynaptic density protein 95; Quin: quinolinic acid; Syn: synaptophysin; SYT1: synaptotagmin 1.
    Figure Legend Snippet: Treatment with NaHS inhibits the dysregulation of neuroplasticity induced by Quin. (A, B) Immunofluorescence images showing colocalization of PSD95 (red, CoraLite594 fluorescent dye) and NeuN (green, CoraLite488 fluorescent dye) in nine coronal sections from three mice per group. PSD95 expression was significantly upregulated in neuronal cells in the Quin + NaHS group compared with the Quin group, and this effect was reversed by the addition of ML385. Scale bar: 20 μm. (C) Western blot was used to measure PSD95, SYT1, and Syn expression levels 6 days after Quin striatal injection. Quantification of PSD95, SYT1, and Syn expression levels ( n = 3 per group). The values are reported as mean ± SD. *** P < 0.001 (one-way analysis of variance followed by Bonferroni post hoc test). NeuN: Neuronal nuclei; PSD95: postsynaptic density protein 95; Quin: quinolinic acid; Syn: synaptophysin; SYT1: synaptotagmin 1.

    Techniques Used: Immunofluorescence, Expressing, Western Blot, Injection



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    86
    Proteintech rabbit polyclonal anti psd95 specific antibody
    Reagents and instruments used in the study
    Rabbit Polyclonal Anti Psd95 Specific Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti psd95 specific antibody/product/Proteintech
    Average 86 stars, based on 1 article reviews
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    Proteintech rabbit polyclonal psd95
    Effects of PBMT on dendritic atrophy and expression of GluA1 in the cortex and hippocampus of depressed mice. (a) Typical staining of MAP2 (green) in the cortex and hippocampal regions from CUMS mice with or without PBMT and the control group. Nuclei were counterstained with DAPI (blue). Scale bar, 100 μ m ( n = 6 per group). (b) Representative immunofluorescent image analysis of NeuN-positive cells (red) in the hippocampal and cortex regions of each group; scale bar represents 100 μ m. (c) Quantification of MAP2 density in the hippocampal and cortex regions of different groups. (d) Quantitative analyses of the NeuN-positive cells in the hippocampal and cortex regions of different groups. (e) Western blot and quantification analysis of MAP2 from control vs. chronic stressed mice without or with PBMT treatment ( n = 6-8 per group). (f) Western blot and quantification analysis of GluA1 from control vs. chronic stressed mice without or with PBMT treatment. (g) Representative western blot and quantification analysis of S845 in chronic stressed mice under the treatment with or without PBMT. (h) Western blot and quantification analysis of <t>PSD95</t> from control vs. chronic stressed mice without or with PBMT treatment. All the data represent mean ± SEM. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001, one-way ANOVA with Tukey's post hoc analysis. MAP2: microtubule-associated protein 2; PSD95: postsynaptic density 95.
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    Proteintech rabbit polyclonal
    Primary antibodies used for immunohistochemistry.
    Rabbit Polyclonal, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Proteintech rabbit polyclonal anti psd 95 antibody
    (A,B) Co-localization of REST with LC3-II, a marker of cellular autophagosomes, in the cytoplasm of the cortex in 263K-infected hamsters. (A) Confocal immunofluorescence labeling for REST (red), LC3-II (green) and nucleus (DAPI, blue) in the brain of the normal control and the 263K-infected hamsters. (B) Quantitative analysis of immunofluorescence in (A) . Relative AFU values (LC3-II/REST ratio) are expressed as fold change relative to the normal control. Data are presented as mean ± SD of triplicate experiments. ∗∗ P < 0.01 vs. the normal control. (C,D) Analyses of Akt-mTOR and LRP6-Wnt-β-catenin signaling pathway molecules in brains of normal control and 263K-infected hamsters. (C) Immunoblots of total mTOR protein, p-mTOR (Ser2448), LRP6, total β-catenin protein, p-β-catenin (Ser552), <t>PSD-95,</t> total Akt protein, p-Akt (Ser473), total GSK-3β protein, p-GSK-3β(Ser9), Synaptophysin (SYP) and Bcl-2 in brain homogenates of normal and 263K-inefcted hamsters. (D) and (E) Quantitative analyses of (C) . Immunoblot density in (D) was normalized to GAPDH and expressed as the ratio to the GAPDH density. Immunoblot density in (E) showed the quantification of p-mTOR (Ser2448)/total mTOR protein, p-β-catenin (Ser552)/total β-catenin protein, p-Akt (Ser473)/total Akt protein and p-GSK3β (Ser9)/total GSK3β protein, total mTOR, β-catenin, Akt and GSK3β protein were normalized to GAPDH. Data are presented as mean ± SD of triplicate experiments. Immunoblotting density was expressed as a ratio to the less amount group for each protein, ∗∗ P < 0.01, ∗∗∗ P < 0.001 vs. the normal control.
    Rabbit Polyclonal Anti Psd 95 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti psd 95 antibody/product/Proteintech
    Average 95 stars, based on 1 article reviews
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    Proteintech rabbit polyclonal anti postsynaptic density protein 95 antibody
    (A,B) Co-localization of REST with LC3-II, a marker of cellular autophagosomes, in the cytoplasm of the cortex in 263K-infected hamsters. (A) Confocal immunofluorescence labeling for REST (red), LC3-II (green) and nucleus (DAPI, blue) in the brain of the normal control and the 263K-infected hamsters. (B) Quantitative analysis of immunofluorescence in (A) . Relative AFU values (LC3-II/REST ratio) are expressed as fold change relative to the normal control. Data are presented as mean ± SD of triplicate experiments. ∗∗ P < 0.01 vs. the normal control. (C,D) Analyses of Akt-mTOR and LRP6-Wnt-β-catenin signaling pathway molecules in brains of normal control and 263K-infected hamsters. (C) Immunoblots of total mTOR protein, p-mTOR (Ser2448), LRP6, total β-catenin protein, p-β-catenin (Ser552), <t>PSD-95,</t> total Akt protein, p-Akt (Ser473), total GSK-3β protein, p-GSK-3β(Ser9), Synaptophysin (SYP) and Bcl-2 in brain homogenates of normal and 263K-inefcted hamsters. (D) and (E) Quantitative analyses of (C) . Immunoblot density in (D) was normalized to GAPDH and expressed as the ratio to the GAPDH density. Immunoblot density in (E) showed the quantification of p-mTOR (Ser2448)/total mTOR protein, p-β-catenin (Ser552)/total β-catenin protein, p-Akt (Ser473)/total Akt protein and p-GSK3β (Ser9)/total GSK3β protein, total mTOR, β-catenin, Akt and GSK3β protein were normalized to GAPDH. Data are presented as mean ± SD of triplicate experiments. Immunoblotting density was expressed as a ratio to the less amount group for each protein, ∗∗ P < 0.01, ∗∗∗ P < 0.001 vs. the normal control.
    Rabbit Polyclonal Anti Postsynaptic Density Protein 95 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Reagents and instruments used in the study

    Journal: Neural Regeneration Research

    Article Title: Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2

    doi: 10.4103/NRR.NRR-D-23-01051

    Figure Lengend Snippet: Reagents and instruments used in the study

    Article Snippet: Rabbit polyclonal anti-PSD95-specific antibody , Proteintech Group , 20665-1-AP (RRID: AB_2687961).

    Techniques: CCK-8 Assay, Saline, TUNEL Assay, DNA Extraction, Modification, Marker, Fluorescence, Microscopy, Imaging

    Treatment with NaHS inhibits the dysregulation of neuroplasticity induced by Quin. (A, B) Immunofluorescence images showing colocalization of PSD95 (red, CoraLite594 fluorescent dye) and NeuN (green, CoraLite488 fluorescent dye) in nine coronal sections from three mice per group. PSD95 expression was significantly upregulated in neuronal cells in the Quin + NaHS group compared with the Quin group, and this effect was reversed by the addition of ML385. Scale bar: 20 μm. (C) Western blot was used to measure PSD95, SYT1, and Syn expression levels 6 days after Quin striatal injection. Quantification of PSD95, SYT1, and Syn expression levels ( n = 3 per group). The values are reported as mean ± SD. *** P < 0.001 (one-way analysis of variance followed by Bonferroni post hoc test). NeuN: Neuronal nuclei; PSD95: postsynaptic density protein 95; Quin: quinolinic acid; Syn: synaptophysin; SYT1: synaptotagmin 1.

    Journal: Neural Regeneration Research

    Article Title: Hydrogen sulfide reduces oxidative stress in Huntington’s disease via Nrf2

    doi: 10.4103/NRR.NRR-D-23-01051

    Figure Lengend Snippet: Treatment with NaHS inhibits the dysregulation of neuroplasticity induced by Quin. (A, B) Immunofluorescence images showing colocalization of PSD95 (red, CoraLite594 fluorescent dye) and NeuN (green, CoraLite488 fluorescent dye) in nine coronal sections from three mice per group. PSD95 expression was significantly upregulated in neuronal cells in the Quin + NaHS group compared with the Quin group, and this effect was reversed by the addition of ML385. Scale bar: 20 μm. (C) Western blot was used to measure PSD95, SYT1, and Syn expression levels 6 days after Quin striatal injection. Quantification of PSD95, SYT1, and Syn expression levels ( n = 3 per group). The values are reported as mean ± SD. *** P < 0.001 (one-way analysis of variance followed by Bonferroni post hoc test). NeuN: Neuronal nuclei; PSD95: postsynaptic density protein 95; Quin: quinolinic acid; Syn: synaptophysin; SYT1: synaptotagmin 1.

    Article Snippet: Rabbit polyclonal anti-PSD95-specific antibody , Proteintech Group , 20665-1-AP (RRID: AB_2687961).

    Techniques: Immunofluorescence, Expressing, Western Blot, Injection

    Effects of PBMT on dendritic atrophy and expression of GluA1 in the cortex and hippocampus of depressed mice. (a) Typical staining of MAP2 (green) in the cortex and hippocampal regions from CUMS mice with or without PBMT and the control group. Nuclei were counterstained with DAPI (blue). Scale bar, 100 μ m ( n = 6 per group). (b) Representative immunofluorescent image analysis of NeuN-positive cells (red) in the hippocampal and cortex regions of each group; scale bar represents 100 μ m. (c) Quantification of MAP2 density in the hippocampal and cortex regions of different groups. (d) Quantitative analyses of the NeuN-positive cells in the hippocampal and cortex regions of different groups. (e) Western blot and quantification analysis of MAP2 from control vs. chronic stressed mice without or with PBMT treatment ( n = 6-8 per group). (f) Western blot and quantification analysis of GluA1 from control vs. chronic stressed mice without or with PBMT treatment. (g) Representative western blot and quantification analysis of S845 in chronic stressed mice under the treatment with or without PBMT. (h) Western blot and quantification analysis of PSD95 from control vs. chronic stressed mice without or with PBMT treatment. All the data represent mean ± SEM. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001, one-way ANOVA with Tukey's post hoc analysis. MAP2: microtubule-associated protein 2; PSD95: postsynaptic density 95.

    Journal: Oxidative Medicine and Cellular Longevity

    Article Title: Photobiomodulation Therapy Ameliorates Glutamatergic Dysfunction in Mice with Chronic Unpredictable Mild Stress-Induced Depression

    doi: 10.1155/2021/6678276

    Figure Lengend Snippet: Effects of PBMT on dendritic atrophy and expression of GluA1 in the cortex and hippocampus of depressed mice. (a) Typical staining of MAP2 (green) in the cortex and hippocampal regions from CUMS mice with or without PBMT and the control group. Nuclei were counterstained with DAPI (blue). Scale bar, 100 μ m ( n = 6 per group). (b) Representative immunofluorescent image analysis of NeuN-positive cells (red) in the hippocampal and cortex regions of each group; scale bar represents 100 μ m. (c) Quantification of MAP2 density in the hippocampal and cortex regions of different groups. (d) Quantitative analyses of the NeuN-positive cells in the hippocampal and cortex regions of different groups. (e) Western blot and quantification analysis of MAP2 from control vs. chronic stressed mice without or with PBMT treatment ( n = 6-8 per group). (f) Western blot and quantification analysis of GluA1 from control vs. chronic stressed mice without or with PBMT treatment. (g) Representative western blot and quantification analysis of S845 in chronic stressed mice under the treatment with or without PBMT. (h) Western blot and quantification analysis of PSD95 from control vs. chronic stressed mice without or with PBMT treatment. All the data represent mean ± SEM. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001, one-way ANOVA with Tukey's post hoc analysis. MAP2: microtubule-associated protein 2; PSD95: postsynaptic density 95.

    Article Snippet: Rabbit polyclonal MAP2 (17490-1-AP), rabbit polyclonal NeuN (26975-1-AP), and rabbit polyclonal PSD95 (20665-1-AP) were purchased from ProteinTech.

    Techniques: Expressing, Staining, Western Blot

    Primary antibodies used for immunohistochemistry.

    Journal: Frontiers in Cellular Neuroscience

    Article Title: Novel Scalable and Simplified System to Generate Microglia-Containing Cerebral Organoids From Human Induced Pluripotent Stem Cells

    doi: 10.3389/fncel.2021.682272

    Figure Lengend Snippet: Primary antibodies used for immunohistochemistry.

    Article Snippet: PSD95 , Rabbit polyclonal , Proteintech, cat. no. 20665–1-AP , 1:400.

    Techniques: Immunohistochemistry

    (A,B) Co-localization of REST with LC3-II, a marker of cellular autophagosomes, in the cytoplasm of the cortex in 263K-infected hamsters. (A) Confocal immunofluorescence labeling for REST (red), LC3-II (green) and nucleus (DAPI, blue) in the brain of the normal control and the 263K-infected hamsters. (B) Quantitative analysis of immunofluorescence in (A) . Relative AFU values (LC3-II/REST ratio) are expressed as fold change relative to the normal control. Data are presented as mean ± SD of triplicate experiments. ∗∗ P < 0.01 vs. the normal control. (C,D) Analyses of Akt-mTOR and LRP6-Wnt-β-catenin signaling pathway molecules in brains of normal control and 263K-infected hamsters. (C) Immunoblots of total mTOR protein, p-mTOR (Ser2448), LRP6, total β-catenin protein, p-β-catenin (Ser552), PSD-95, total Akt protein, p-Akt (Ser473), total GSK-3β protein, p-GSK-3β(Ser9), Synaptophysin (SYP) and Bcl-2 in brain homogenates of normal and 263K-inefcted hamsters. (D) and (E) Quantitative analyses of (C) . Immunoblot density in (D) was normalized to GAPDH and expressed as the ratio to the GAPDH density. Immunoblot density in (E) showed the quantification of p-mTOR (Ser2448)/total mTOR protein, p-β-catenin (Ser552)/total β-catenin protein, p-Akt (Ser473)/total Akt protein and p-GSK3β (Ser9)/total GSK3β protein, total mTOR, β-catenin, Akt and GSK3β protein were normalized to GAPDH. Data are presented as mean ± SD of triplicate experiments. Immunoblotting density was expressed as a ratio to the less amount group for each protein, ∗∗ P < 0.01, ∗∗∗ P < 0.001 vs. the normal control.

    Journal: Frontiers in Molecular Neuroscience

    Article Title: Downregulation of the Repressor Element 1-Silencing Transcription Factor (REST) Is Associated with Akt-mTOR and Wnt-β-Catenin Signaling in Prion Diseases Models

    doi: 10.3389/fnmol.2017.00128

    Figure Lengend Snippet: (A,B) Co-localization of REST with LC3-II, a marker of cellular autophagosomes, in the cytoplasm of the cortex in 263K-infected hamsters. (A) Confocal immunofluorescence labeling for REST (red), LC3-II (green) and nucleus (DAPI, blue) in the brain of the normal control and the 263K-infected hamsters. (B) Quantitative analysis of immunofluorescence in (A) . Relative AFU values (LC3-II/REST ratio) are expressed as fold change relative to the normal control. Data are presented as mean ± SD of triplicate experiments. ∗∗ P < 0.01 vs. the normal control. (C,D) Analyses of Akt-mTOR and LRP6-Wnt-β-catenin signaling pathway molecules in brains of normal control and 263K-infected hamsters. (C) Immunoblots of total mTOR protein, p-mTOR (Ser2448), LRP6, total β-catenin protein, p-β-catenin (Ser552), PSD-95, total Akt protein, p-Akt (Ser473), total GSK-3β protein, p-GSK-3β(Ser9), Synaptophysin (SYP) and Bcl-2 in brain homogenates of normal and 263K-inefcted hamsters. (D) and (E) Quantitative analyses of (C) . Immunoblot density in (D) was normalized to GAPDH and expressed as the ratio to the GAPDH density. Immunoblot density in (E) showed the quantification of p-mTOR (Ser2448)/total mTOR protein, p-β-catenin (Ser552)/total β-catenin protein, p-Akt (Ser473)/total Akt protein and p-GSK3β (Ser9)/total GSK3β protein, total mTOR, β-catenin, Akt and GSK3β protein were normalized to GAPDH. Data are presented as mean ± SD of triplicate experiments. Immunoblotting density was expressed as a ratio to the less amount group for each protein, ∗∗ P < 0.01, ∗∗∗ P < 0.001 vs. the normal control.

    Article Snippet: Rabbit polyclonal anti-REST antibody (22242-1-AP) (1:200), mouse monoclonal anti-LC3-II antibody (66139-1-lg) (1:200), rabbit polyclonal anti-Synaptophysin antibody (17785-1-AP) (1:200), rabbit polyclonal anti-PSD-95 antibody (20665-1-AP) (1:200), the rabbit polyclonal anti-Akt antibody (10176-2-AP) (1:200), rabbit polyclonal anti-beta-Catenin antibody (51067-2-AP) (1:200), rabbit polyclonal anti-GSK3β antibody (22104-1-AP) (1:200), mouse monoclonal anti-GAPDH antibody (60004-1-lg) (1:1000), and rabbit polyclonal anti-Lamin B1 antibody (12987-1-AP) (1:500) were purchased from Proteintech Biotechnology (Chicago, IL, USA).

    Techniques: Marker, Infection, Immunofluorescence, Labeling, Western Blot