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rabbit polyclonal anti-darpp32  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit polyclonal anti-darpp32
    Rabbit Polyclonal Anti Darpp32, supplied by Santa Cruz Biotechnology, 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/rabbit polyclonal anti-darpp32/product/Santa Cruz Biotechnology
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal anti-darpp32 - by Bioz Stars, 2026-02
    90/100 stars

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    Cell Signaling Technology Inc polyclonal rabbit anti darpp32 thr75 antibody
    Effect of treatment (Veh-Veh, TBZ-Veh, Veh-BUP, or TBZ-BUP) on number of cell counts positive for pDARPP-32-(Thr34) and <t>pDARPP-32(Thr75)</t> immunoreactivity on Nacb core. Upper left: Diagram showing the effect of TBZ on DARPP-32 phosphorylation in D2-receptor containing cells, and coronal section with bregma coordinates showing location of the brain area for immunohistochemistry taken from Paxino and Franklin’s mouse atlas. TBZ, which depletes DA, increases D2-receptor stimulation by increasing cyclic adenosine monophosphate (c-AMP) production and protein kinase A (PKA) activity yielding to the increase of the dephosphorylation of pDARPP-32(Thr34) and no change or a decrease in the phosphorylation of pDARPP-32(Thr75) by blocking the protein phosphatase (PP1) (based on results from Bateup et al. ; Nunes et al. ; López-Cruz et al. ). Bottom left: photomicrographs of individual representative brain sections. Right: mean ± S.E.M of number of pDARPP-32-(Thr34) and pDARPP-32-(Thr75) counts in a 100um 2 ROI. * p < 0.05, ** p < 0.01 significantly different from Veh-Veh. ## p < 0.01 significant differences from TBZ-Veh
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    Effect of treatment (Veh-Veh, TBZ-Veh, Veh-BUP, or TBZ-BUP) on number of cell counts positive for pDARPP-32-(Thr34) and pDARPP-32(Thr75) immunoreactivity on Nacb core. Upper left: Diagram showing the effect of TBZ on DARPP-32 phosphorylation in D2-receptor containing cells, and coronal section with bregma coordinates showing location of the brain area for immunohistochemistry taken from Paxino and Franklin’s mouse atlas. TBZ, which depletes DA, increases D2-receptor stimulation by increasing cyclic adenosine monophosphate (c-AMP) production and protein kinase A (PKA) activity yielding to the increase of the dephosphorylation of pDARPP-32(Thr34) and no change or a decrease in the phosphorylation of pDARPP-32(Thr75) by blocking the protein phosphatase (PP1) (based on results from Bateup et al. ; Nunes et al. ; López-Cruz et al. ). Bottom left: photomicrographs of individual representative brain sections. Right: mean ± S.E.M of number of pDARPP-32-(Thr34) and pDARPP-32-(Thr75) counts in a 100um 2 ROI. * p < 0.05, ** p < 0.01 significantly different from Veh-Veh. ## p < 0.01 significant differences from TBZ-Veh

    Journal: Psychopharmacology

    Article Title: Energizing effects of bupropion on effortful behaviors in mice under positive and negative test conditions: modulation of DARPP-32 phosphorylation patterns

    doi: 10.1007/s00213-021-05950-4

    Figure Lengend Snippet: Effect of treatment (Veh-Veh, TBZ-Veh, Veh-BUP, or TBZ-BUP) on number of cell counts positive for pDARPP-32-(Thr34) and pDARPP-32(Thr75) immunoreactivity on Nacb core. Upper left: Diagram showing the effect of TBZ on DARPP-32 phosphorylation in D2-receptor containing cells, and coronal section with bregma coordinates showing location of the brain area for immunohistochemistry taken from Paxino and Franklin’s mouse atlas. TBZ, which depletes DA, increases D2-receptor stimulation by increasing cyclic adenosine monophosphate (c-AMP) production and protein kinase A (PKA) activity yielding to the increase of the dephosphorylation of pDARPP-32(Thr34) and no change or a decrease in the phosphorylation of pDARPP-32(Thr75) by blocking the protein phosphatase (PP1) (based on results from Bateup et al. ; Nunes et al. ; López-Cruz et al. ). Bottom left: photomicrographs of individual representative brain sections. Right: mean ± S.E.M of number of pDARPP-32-(Thr34) and pDARPP-32-(Thr75) counts in a 100um 2 ROI. * p < 0.05, ** p < 0.01 significantly different from Veh-Veh. ## p < 0.01 significant differences from TBZ-Veh

    Article Snippet: Equal amounts (30ug) of striatum protein samples were separated by 12.5% SDS-PAGE and transferred to nitrocellulose membrane (Bio-rad) for 90 min at 30 V. Filtering membranes were incubated in 5% of bovine serum albumin (BSA, Sigma-Aldrich) dissolved in TBS-T (Tris Base 200 Mm and 5 M NaCl) containing 0.1% Tween 20, and then incubated overnight at 4 °C with polyclonal rabbit anti-DARPP32-Thr75 antibody (1:500, cell signaling).

    Techniques: Phospho-proteomics, Immunohistochemistry, Activity Assay, De-Phosphorylation Assay, Blocking Assay

    Effect of treatment (Veh-Veh, TBZ-Veh, Veh-BUP, or TBZ-BUP) on pDARPP-32 (Thr75) in ventral striatum. Data are expressed as mean ± S.E.M of density units of pDARPP-32 (Thr75). Lower and right part: representative Western blots showing two bands corresponding to actin (molecular weight of 42 kDa) and pDARPP-32(Thr75) (molecular weight of 32 kDa). Each line contains 30ug of ventral striatum homogenates taken as tissue punctures represented in the coronal brain sections

    Journal: Psychopharmacology

    Article Title: Energizing effects of bupropion on effortful behaviors in mice under positive and negative test conditions: modulation of DARPP-32 phosphorylation patterns

    doi: 10.1007/s00213-021-05950-4

    Figure Lengend Snippet: Effect of treatment (Veh-Veh, TBZ-Veh, Veh-BUP, or TBZ-BUP) on pDARPP-32 (Thr75) in ventral striatum. Data are expressed as mean ± S.E.M of density units of pDARPP-32 (Thr75). Lower and right part: representative Western blots showing two bands corresponding to actin (molecular weight of 42 kDa) and pDARPP-32(Thr75) (molecular weight of 32 kDa). Each line contains 30ug of ventral striatum homogenates taken as tissue punctures represented in the coronal brain sections

    Article Snippet: Equal amounts (30ug) of striatum protein samples were separated by 12.5% SDS-PAGE and transferred to nitrocellulose membrane (Bio-rad) for 90 min at 30 V. Filtering membranes were incubated in 5% of bovine serum albumin (BSA, Sigma-Aldrich) dissolved in TBS-T (Tris Base 200 Mm and 5 M NaCl) containing 0.1% Tween 20, and then incubated overnight at 4 °C with polyclonal rabbit anti-DARPP32-Thr75 antibody (1:500, cell signaling).

    Techniques: Western Blot, Molecular Weight

    Journal: Cell reports

    Article Title: Single-Cell Analysis of Foxp1-Driven Mechanisms Essential for Striatal Development

    doi: 10.1016/j.celrep.2020.02.030

    Figure Lengend Snippet:

    Article Snippet: Rabbit polyclonal anti-DARPP32 , Millipore , Cat#: AB10518, RRID:AB_10807019.

    Techniques: Recombinant, SYBR Green Assay, Software, Transgenic Assay