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rabbit anti d2r extracellular antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs rabbit anti d2r extracellular antibody
    Rabbit Anti D2r Extracellular Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+dopamine+d2+receptor/Anti-D2+Dopamine+Receptor+Antibody/pm41642719-163-0-8
    Average 94 stars, based on 14 article reviews
    rabbit anti d2r extracellular antibody - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Western Blot:

    Article Title: Modulation of Theta-Band Local Field Potential Oscillations Across Brain Networks With Central Thalamic Deep Brain Stimulation to Enhance Spatial Working Memory
    Article Snippet: Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).. The membranes were hybridized with the anti-dopamine D2 receptor (DRD2, 1:1000 dilution; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-dopamine D1 receptor (DRD1, 1:1000 dilution; DR001AN03, Alomone Labs, Jerusalem, Israel) antibodies or anicotinic acetylcholine receptor alpha 4 (α4-nAChR, 1:1000 dilution; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).

    Article Title: Central Thalamic Deep-Brain Stimulation Alters Striatal-Thalamic Connectivity in Cognitive Neural Behavior
    Article Snippet: Protein samples were extracted in ice-cold lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA).lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). ... The membranes were hybridized with anti-dopamine D2 receptor (Drd2; 1:1000; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-nicotinic acetylcholine α 4 receptor (α4-nAChR; 1:1000; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).

    SDS Page:

    Article Title: Modulation of Theta-Band Local Field Potential Oscillations Across Brain Networks With Central Thalamic Deep Brain Stimulation to Enhance Spatial Working Memory
    Article Snippet: Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).. The membranes were hybridized with the anti-dopamine D2 receptor (DRD2, 1:1000 dilution; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-dopamine D1 receptor (DRD1, 1:1000 dilution; DR001AN03, Alomone Labs, Jerusalem, Israel) antibodies or anicotinic acetylcholine receptor alpha 4 (α4-nAChR, 1:1000 dilution; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).

    Article Title: Central Thalamic Deep-Brain Stimulation Alters Striatal-Thalamic Connectivity in Cognitive Neural Behavior
    Article Snippet: Protein samples were extracted in ice-cold lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA).lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). ... The membranes were hybridized with anti-dopamine D2 receptor (Drd2; 1:1000; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-nicotinic acetylcholine α 4 receptor (α4-nAChR; 1:1000; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).

    Expressing:

    Article Title: Modulation of Theta-Band Local Field Potential Oscillations Across Brain Networks With Central Thalamic Deep Brain Stimulation to Enhance Spatial Working Memory
    Article Snippet: Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).. The membranes were hybridized with the anti-dopamine D2 receptor (DRD2, 1:1000 dilution; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-dopamine D1 receptor (DRD1, 1:1000 dilution; DR001AN03, Alomone Labs, Jerusalem, Israel) antibodies or anicotinic acetylcholine receptor alpha 4 (α4-nAChR, 1:1000 dilution; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).

    Article Title: Central Thalamic Deep-Brain Stimulation Alters Striatal-Thalamic Connectivity in Cognitive Neural Behavior
    Article Snippet: Protein samples were extracted in ice-cold lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA).lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). ... The membranes were hybridized with anti-dopamine D2 receptor (Drd2; 1:1000; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-nicotinic acetylcholine α 4 receptor (α4-nAChR; 1:1000; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).

    Control:

    Article Title: Modulation of Theta-Band Local Field Potential Oscillations Across Brain Networks With Central Thalamic Deep Brain Stimulation to Enhance Spatial Working Memory
    Article Snippet: Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).Gels were then transferred onto polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States).. The membranes were hybridized with the anti-dopamine D2 receptor (DRD2, 1:1000 dilution; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-dopamine D1 receptor (DRD1, 1:1000 dilution; DR001AN03, Alomone Labs, Jerusalem, Israel) antibodies or anicotinic acetylcholine receptor alpha 4 (α4-nAChR, 1:1000 dilution; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).Next, the membranes were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, United States) and developed using the Luminata Forte Western HRP substrate (Millipore, Billerica, MA, United States).

    Article Title: Central Thalamic Deep-Brain Stimulation Alters Striatal-Thalamic Connectivity in Cognitive Neural Behavior
    Article Snippet: Protein samples were extracted in ice-cold lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA).lysis buffer (50 mM Tris-HCl, pH = 7.5, 0.3 M sucrose, 5 mM EDTA, 2 mM sodium pyrophosphate, 1 mM sodium orthovanadate, 1 mM PMSF, 20 μg/ml leupeptin, and 4 μg/ml aprotinin) and then separated (30 μg) by SDS-PAGE, and trans-blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). ... The membranes were hybridized with anti-dopamine D2 receptor (Drd2; 1:1000; ADR-002-50UL, Alomone Labs, Jerusalem, Israel) or anti-nicotinic acetylcholine α 4 receptor (α4-nAChR; 1:1000; ANC-004-50UL, Alomone Labs, Jerusalem, Israel) antibodies.. Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).Then, the blots were washed and incubated with HRP-conjugated goat anti-rabbit IgG antibody (1:1000 dilution; Jackson ImmunoResearch Inc., West Grove, PA, USA), and developed by Luminata Forte Western HRP substrate (Millipore, Billerica, MA, USA).



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