rabbit anti darpp 32 Search Results


darpp32  (Bio-Rad)
91
Bio-Rad darpp32
FIGURE 9 Interaction of CHL1 and DRD2 on TH- and DARP32-positive neurons in striatal sections. Proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies was combined with immunostaining using rabbit <t>anti-DARPP32</t> (A) or anti-TH (B) antibodies to analyze tissue sections from 12- to 18-week-old CHL1+/+ mice. Nuclei are stained with DAPI (blue). Representative images are shown. Close- ups of two regions (without DAPI staining) are indicated by boxes and arrowheads indicate red spots indicating close molecular interaction of CHL1 with DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals
Darpp32, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/darpp32/product/Bio-Rad
Average 91 stars, based on 1 article reviews
darpp32 - by Bioz Stars, 2026-03
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rabbit anti-darpp-32  (Covance)
90
Covance rabbit anti-darpp-32
FIGURE 9 Interaction of CHL1 and DRD2 on TH- and DARP32-positive neurons in striatal sections. Proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies was combined with immunostaining using rabbit <t>anti-DARPP32</t> (A) or anti-TH (B) antibodies to analyze tissue sections from 12- to 18-week-old CHL1+/+ mice. Nuclei are stained with DAPI (blue). Representative images are shown. Close- ups of two regions (without DAPI staining) are indicated by boxes and arrowheads indicate red spots indicating close molecular interaction of CHL1 with DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals
Rabbit Anti Darpp 32, supplied by Covance, 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 anti-darpp-32/product/Covance
Average 90 stars, based on 1 article reviews
rabbit anti-darpp-32 - by Bioz Stars, 2026-03
90/100 stars
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rabbit anti-darpp-32 ab10518  (Merck KGaA)
90
Merck KGaA rabbit anti-darpp-32 ab10518
FIGURE 9 Interaction of CHL1 and DRD2 on TH- and DARP32-positive neurons in striatal sections. Proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies was combined with immunostaining using rabbit <t>anti-DARPP32</t> (A) or anti-TH (B) antibodies to analyze tissue sections from 12- to 18-week-old CHL1+/+ mice. Nuclei are stained with DAPI (blue). Representative images are shown. Close- ups of two regions (without DAPI staining) are indicated by boxes and arrowheads indicate red spots indicating close molecular interaction of CHL1 with DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals
Rabbit Anti Darpp 32 Ab10518, supplied by Merck KGaA, 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 anti-darpp-32 ab10518/product/Merck KGaA
Average 90 stars, based on 1 article reviews
rabbit anti-darpp-32 ab10518 - by Bioz Stars, 2026-03
90/100 stars
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rabbit anti–darpp-32  (US Biological Life Sciences)
90
US Biological Life Sciences rabbit anti–darpp-32
Immunohistochemical stainings of dorsal striatum of 2-y-old control (A, D, and G) and DAT-Ret lx/lx mutants (B, E, and H) for NeuN (A and B), <t>DARPP-32</t> (D and E), or parvalbumin (G and H). Histograms showing the number of NeuN-positive (C), DARPP-32–positive (F), and parvalbumin-positive cells (I) in DAT-Ret lx/lx mutants and age-matched controls ( n = 3–5 each genotype). Note also the reduced staining intensities for NeuN and DARPP-32 in DAT-Ret lx/lx compared to control mice. *, p < 0.05; **, p < 0.01 (Student t -test). Scale bars indicate 50 μm.
Rabbit Anti–Darpp 32, supplied by US Biological Life Sciences, 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 anti–darpp-32/product/US Biological Life Sciences
Average 90 stars, based on 1 article reviews
rabbit anti–darpp-32 - by Bioz Stars, 2026-03
90/100 stars
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rabbit polyclonal anti-darpp-32  (Merck KGaA)
90
Merck KGaA rabbit polyclonal anti-darpp-32
Immunohistochemical stainings of dorsal striatum of 2-y-old control (A, D, and G) and DAT-Ret lx/lx mutants (B, E, and H) for NeuN (A and B), <t>DARPP-32</t> (D and E), or parvalbumin (G and H). Histograms showing the number of NeuN-positive (C), DARPP-32–positive (F), and parvalbumin-positive cells (I) in DAT-Ret lx/lx mutants and age-matched controls ( n = 3–5 each genotype). Note also the reduced staining intensities for NeuN and DARPP-32 in DAT-Ret lx/lx compared to control mice. *, p < 0.05; **, p < 0.01 (Student t -test). Scale bars indicate 50 μm.
Rabbit Polyclonal Anti Darpp 32, supplied by Merck KGaA, 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-darpp-32/product/Merck KGaA
Average 90 stars, based on 1 article reviews
rabbit polyclonal anti-darpp-32 - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


FIGURE 9 Interaction of CHL1 and DRD2 on TH- and DARP32-positive neurons in striatal sections. Proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies was combined with immunostaining using rabbit anti-DARPP32 (A) or anti-TH (B) antibodies to analyze tissue sections from 12- to 18-week-old CHL1+/+ mice. Nuclei are stained with DAPI (blue). Representative images are shown. Close- ups of two regions (without DAPI staining) are indicated by boxes and arrowheads indicate red spots indicating close molecular interaction of CHL1 with DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals

Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Article Title: Cell adhesion molecule close homolog of L1 binds to the dopamine receptor D2 and inhibits the internalization of its short isoform.

doi: 10.1096/fj.201900577RRRR

Figure Lengend Snippet: FIGURE 9 Interaction of CHL1 and DRD2 on TH- and DARP32-positive neurons in striatal sections. Proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies was combined with immunostaining using rabbit anti-DARPP32 (A) or anti-TH (B) antibodies to analyze tissue sections from 12- to 18-week-old CHL1+/+ mice. Nuclei are stained with DAPI (blue). Representative images are shown. Close- ups of two regions (without DAPI staining) are indicated by boxes and arrowheads indicate red spots indicating close molecular interaction of CHL1 with DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals

Article Snippet: The polyclonal rabbit antibodies against TH phosphorylated at Ser40 (pSer-TH) (Bio-Rad/AbD Serotec Cat# AHP912, RRID:AB_567401) and against DARPP32 phosphorylated at Thr34 (pThr34-DARPP32) (Bio-Rad/AbD Serotec Cat# AHP897, RRID:AB_566944) were from BioRad (Puchheim, Germany).

Techniques: Proximity Ligation Assay, Immunostaining, Staining

FIGURE 10 Interaction of CHL1 and DRD2 on TH- and DARP32-positive cells in cultures of ventral midbrain and striatum. Cultures of ventral midbrain (A) or striatum (B) were analyzed by proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies combined with immunofluorescent staining using rabbit anti-TH or anti-DARPP32 antibodies. Nuclei are stained with DAPI (blue). Representative images of different cells are shown. Red spots indicate close molecular interaction between CHL1 and DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals

Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Article Title: Cell adhesion molecule close homolog of L1 binds to the dopamine receptor D2 and inhibits the internalization of its short isoform.

doi: 10.1096/fj.201900577RRRR

Figure Lengend Snippet: FIGURE 10 Interaction of CHL1 and DRD2 on TH- and DARP32-positive cells in cultures of ventral midbrain and striatum. Cultures of ventral midbrain (A) or striatum (B) were analyzed by proximity ligation assay using goat anti-CHL1 and mouse anti-DRD2 antibodies combined with immunofluorescent staining using rabbit anti-TH or anti-DARPP32 antibodies. Nuclei are stained with DAPI (blue). Representative images of different cells are shown. Red spots indicate close molecular interaction between CHL1 and DRD2. Scale bars: 10 µm. Three independent experiments were performed with different sets of animals

Article Snippet: The polyclonal rabbit antibodies against TH phosphorylated at Ser40 (pSer-TH) (Bio-Rad/AbD Serotec Cat# AHP912, RRID:AB_567401) and against DARPP32 phosphorylated at Thr34 (pThr34-DARPP32) (Bio-Rad/AbD Serotec Cat# AHP897, RRID:AB_566944) were from BioRad (Puchheim, Germany).

Techniques: Proximity Ligation Assay, Staining

FIGURE 11 Reduced DRD2 and pSer40-TH levels in the dorsal striatum and reduced pThr34-DARPP32 levels in the ventral striatum in the absence of CHL1. The dorsal and ventral parts of the striatum were isolated from 10- to 13-week-old CHL1+/+ and CHL1−/− mice and subjected to Western blot analysis with anti-DRD2 and anti-GAPDH antibodies (A), anti-pSer40-TH and anti-TH antibodies (B) or anti-pThr34-DARPP32 and anti-DARPP32 (C) antibodies. Protein levels were determined by densitometry and DRD2 levels relative to GAPDH levels (A), pSer40-TH levels relative to total TH levels (B) and pThr34-DARPP32 levels relative to total DARPP32 levels (C) were calculated. A-C, Representative Western blots (left panels) are shown and mean values + standard error of the mean from eight CHL1−/− and 11 CHL1+/+ mice (right panels) are shown for the relative levels of DRD2 (A), pSer40-TH (B) and pThr34-DARPP32 (C) (Kruskal-Wallis test with post-hoc Dunn´s multiple comparison test; *P < .05, **P < .01). A, Lanes not adjacent to each other but derived from the same blot are separated by a vertical line

Journal: FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Article Title: Cell adhesion molecule close homolog of L1 binds to the dopamine receptor D2 and inhibits the internalization of its short isoform.

doi: 10.1096/fj.201900577RRRR

Figure Lengend Snippet: FIGURE 11 Reduced DRD2 and pSer40-TH levels in the dorsal striatum and reduced pThr34-DARPP32 levels in the ventral striatum in the absence of CHL1. The dorsal and ventral parts of the striatum were isolated from 10- to 13-week-old CHL1+/+ and CHL1−/− mice and subjected to Western blot analysis with anti-DRD2 and anti-GAPDH antibodies (A), anti-pSer40-TH and anti-TH antibodies (B) or anti-pThr34-DARPP32 and anti-DARPP32 (C) antibodies. Protein levels were determined by densitometry and DRD2 levels relative to GAPDH levels (A), pSer40-TH levels relative to total TH levels (B) and pThr34-DARPP32 levels relative to total DARPP32 levels (C) were calculated. A-C, Representative Western blots (left panels) are shown and mean values + standard error of the mean from eight CHL1−/− and 11 CHL1+/+ mice (right panels) are shown for the relative levels of DRD2 (A), pSer40-TH (B) and pThr34-DARPP32 (C) (Kruskal-Wallis test with post-hoc Dunn´s multiple comparison test; *P < .05, **P < .01). A, Lanes not adjacent to each other but derived from the same blot are separated by a vertical line

Article Snippet: The polyclonal rabbit antibodies against TH phosphorylated at Ser40 (pSer-TH) (Bio-Rad/AbD Serotec Cat# AHP912, RRID:AB_567401) and against DARPP32 phosphorylated at Thr34 (pThr34-DARPP32) (Bio-Rad/AbD Serotec Cat# AHP897, RRID:AB_566944) were from BioRad (Puchheim, Germany).

Techniques: Isolation, Western Blot, Comparison, Derivative Assay

Immunohistochemical stainings of dorsal striatum of 2-y-old control (A, D, and G) and DAT-Ret lx/lx mutants (B, E, and H) for NeuN (A and B), DARPP-32 (D and E), or parvalbumin (G and H). Histograms showing the number of NeuN-positive (C), DARPP-32–positive (F), and parvalbumin-positive cells (I) in DAT-Ret lx/lx mutants and age-matched controls ( n = 3–5 each genotype). Note also the reduced staining intensities for NeuN and DARPP-32 in DAT-Ret lx/lx compared to control mice. *, p < 0.05; **, p < 0.01 (Student t -test). Scale bars indicate 50 μm.

Journal: PLoS Biology

Article Title: Absence of Ret Signaling in Mice Causes Progressive and Late Degeneration of the Nigrostriatal System

doi: 10.1371/journal.pbio.0050039

Figure Lengend Snippet: Immunohistochemical stainings of dorsal striatum of 2-y-old control (A, D, and G) and DAT-Ret lx/lx mutants (B, E, and H) for NeuN (A and B), DARPP-32 (D and E), or parvalbumin (G and H). Histograms showing the number of NeuN-positive (C), DARPP-32–positive (F), and parvalbumin-positive cells (I) in DAT-Ret lx/lx mutants and age-matched controls ( n = 3–5 each genotype). Note also the reduced staining intensities for NeuN and DARPP-32 in DAT-Ret lx/lx compared to control mice. *, p < 0.05; **, p < 0.01 (Student t -test). Scale bars indicate 50 μm.

Article Snippet: Primary antibodies used were goat anti-Ret (1:25; RDI, Flanders, New Jersey, United States, or Neuromics, North Field, Minnesota, United States), monoclonal mouse anti-tyrosine hydroxylase (1:2,000; DiaSorin, Stillwater, Massachusetts, United States), rabbit anti-dopa decarboxylase (1:100; Chemicon/Millipore, Billerica, Massachusetts, United States), monoclonal mouse anti–β-galactosidase (1:50; Sigma, St. Louis, Missouri, United States), rat anti-dopamine transporter (1:500; Chemicon/Millipore), rabbit anti-Pitx3 (1:1,000, provided by M. P. Smidt [ ]), monoclonal mouse anti-NeuN (1:200; Chemicon/Millipore), rabbit anti-GFAP (1:500; DakoCytomation, Glostrup, Denmark), rabbit anti–DARPP-32 (1:50; United States Biological, Swampscott, Massachusetts, United States), monoclonal mouse anti-parvalbumin (1:10,000; Swant, Bellinzona, Switzerland), rabbit anti–Iba-1 (1:1,000; Wako, Neuss, Germany), monoclonal rat anti-MAC1 (1:200; Serotec, Kidlington, United Kingdom).

Techniques: Immunohistochemical staining, Staining