rabbit monoclonal anti darpp32  (Cell Signaling Technology Inc)

Journal: Frontiers in Aging Neuroscience

Article Title: Abnormal outer and inner retina in a mouse model of Huntington’s disease with age

doi: 10.3389/fnagi.2024.1434551

Figure Lengend Snippet: Information of antibodies used in Western blotting.

Article Snippet: Rabbit monoclonal anti-Darpp32 , Cell signaling, Danvers, Massachusetts, USA , 2306S , , 1:1000 , Brain.

Techniques: Western Blot

Journal: Frontiers in Aging Neuroscience

Article Title: Abnormal outer and inner retina in a mouse model of Huntington’s disease with age

doi: 10.3389/fnagi.2024.1434551

Figure Lengend Snippet: Information on antibodies used in immunofluorescent staining.

Article Snippet: Rabbit monoclonal anti-Darpp32 , Cell signaling, Danvers, Massachusetts, USA , 2306S , , 1:1000 , Brain.

Techniques: Staining, Electron Microscopy

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 rabbit monoclonal antibody against DARPP32 (Cell Signaling Technology Cat# 2306, RRID:AB_823479) was from Cell Signaling Technology Europe (Frankfurt am Main, Germany) and the polyclonal rabbit antibody against tyrosine hydroxylase (TH) (Millipore Cat# AB152, RRID:AB_390204) was from Merck Chemicals (Darmstadt, Germany).

Techniques: Proximity Ligation Assay, Immunostaining, Staining

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 rabbit monoclonal antibody against DARPP32 (Cell Signaling Technology Cat# 2306, RRID:AB_823479) was from Cell Signaling Technology Europe (Frankfurt am Main, Germany) and the polyclonal rabbit antibody against tyrosine hydroxylase (TH) (Millipore Cat# AB152, RRID:AB_390204) was from Merck Chemicals (Darmstadt, Germany).

Techniques: Proximity Ligation Assay, Staining

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 rabbit monoclonal antibody against DARPP32 (Cell Signaling Technology Cat# 2306, RRID:AB_823479) was from Cell Signaling Technology Europe (Frankfurt am Main, Germany) and the polyclonal rabbit antibody against tyrosine hydroxylase (TH) (Millipore Cat# AB152, RRID:AB_390204) was from Merck Chemicals (Darmstadt, Germany).

Techniques: Isolation, Western Blot, Comparison, Derivative Assay

Journal: eLife

Article Title: Cell-type-specific regulation of neuronal intrinsic excitability by macroautophagy

doi: 10.7554/eLife.50843

Figure Lengend Snippet:

Article Snippet: Antibody , Rabbit anti-DARPP32 monoclonal , Cell Signaling Technology , Cat # 2306S , See Table S3 in .

Techniques: Transformation Assay, Bioprocessing, Ubiquitin Proteomics, Magnetic Beads, Recombinant, Plasmid Preparation, Sequencing, RNAscope, Multiplex Assay, Bicinchoninic Acid Protein Assay, Western Blot, Protease Inhibitor, Software