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goat anti-dat  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology goat anti-dat
    Goat Anti Dat, 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/product/goat+anti+dat/goat+polyclonal+anti+dat+antibody++k+20/bio_rxiv__2025__03__21__644417-247-22-25
    Average 90 stars, based on 1 article reviews
    goat anti-dat - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Incubation:

    Article Title: Inhibition of Nigral Microglial Activation Reduces Age-Related Loss of Dopaminergic Neurons and Motor Deficits
    Article Snippet: The free-floating 30-micrometer brain sections of interest were selected, washed with 0.3% Triton X-100 (X100, Sigma-Aldrich, St. Louis, MO, USA) in PBS, immersed in 3% H 2 O 2 to abolish endogenous peroxidase activity, and blocked with 3% normal goat serum (Cat# 005-000-001, RRID: AB_2336983, Jackson ImmunoResearch Inc., West Grove, PA, USA) to reduce non-specific bindings of antibody for 1 h at room temperature. .. The sections were then incubated with rabbit anti-tyrosine hydroxylase (TH) (1:2000; MAB152, Millipore, Darmstadt, Germany) for DA neurons, rabbit anti-ionized calcium-binding adapter molecule-1 (Iba1) (1:2000; 019-19741, Wako Pure Chemical Industries, Osaka, Japan) for microglia, and goat anti-DAT (1:1000; SC-1433, Santa Cruz Biotechnology, Dallas, TX, USA) for DA neuron terminals. .. Sections were then incubated with appropriate biotin-conjugated secondary antibodies and avidin-biotin-peroxidase (PK-6100, Vectastain Elite ABC Kit, Vector Laboratories, Burlingame, CA, USA) using diaminobenzidine to visualize signals.

    Article Title: [ 3 H]Dopamine Uptake through the Dopamine and Norepinephrine Transporters is Decreased in the Prefrontal Cortex of Transgenic Mice Expressing HIV-1 Transactivator of Transcription Protein
    Article Snippet: .. Samples were separated by 10% SDS-polyacrylamide gel electrophoresis for ∼90 minutes at 125 V. Samples were then transferred to Immobilon-P transfer membranes (0.45-μm pore size; Millipore Co., Bedford, MA) in transfer buffer (50 mM Tris, 250 mM glycine, 3.5 mM SDS) using a Mini Trans-Blot Electrophoretic Transfer Cell (Bio-Rad, Hercules, CA) for 90 minutes at 75 V. The membranes were then incubated with blocking buffer (5% milk powder in PBS containing 0.5% Tween-20) for 1 hour at room temperature, followed by incubation with either goat anti-DAT (C-20 polyclonal antibody, diluted 1:500 in blocking buffer; Santa Cruz) or mouse anti-NET (MAb tech, 05-1 monoclonal antibody, diluted 1:5000 in blocking buffer) overnight at 4°C. .. Transfer membranes were then washed three times with blocking buffer at room temperature, followed by incubation with either anti-goat horseradish peroxidase (catalog number 305-035-045, diluted 1:10,000 in blocking buffer; Jackson Laboratory) or anti-mouse horseradish peroxidase (catalog number 7076S, diluted 1:15,000 in blocking buffer; Cell Signaling) for 1 hour at room temperature.

    Article Title: Evidence for an Additive Neurorestorative Effect of Simultaneously Administered CDNF and GDNF in Hemiparkinsonian Rats: Implications for Different Mechanism of Action
    Article Snippet: .. After transfer of proteins to a nitrocellulose membrane, the membrane was incubated in 5% BSA for 1.5 h to block unspecific binding and then incubated in the presence of mouse anti-TH (1:5000, MAB 318, Millipore), goat anti-DAT (1:1000, sc2020, Santa Cruz Biotechnology), mouse anti-β-actin (1:2000, A1978, Sigma-Aldrich), rabbit anti-pERK (1:1000, 9101, Cell Signaling), rabbit anti-ERK (1:1000, 9102, Cell Signaling), rabbit anti-pAkt (1:2000, 9271, Cell Signaling), rabbit anti-Akt (1:1000, 9272, Cell Signaling), rabbit anti-p-eukaryotic initiation factor 2α subunit (eIF2α) (1:1000, 3398, Cell Signaling), rabbit anti-eIF2α (1:1000, 9722, Cell Signaling), rabbit anti-GRP78 (1:1000, sc-1051, Santa Cruz Biotechnology), and mouse anti-β-tubuline antibodies at 4°C overnight. .. Membranes were further incubated in horseradish peroxidase-conjugated secondary antibodies [goat anti-mouse 1:2000 (R&D Systems), donkey anti-goat 1:1000 (Santa Cruz Biotechnology), or donkey anti-rabbit 1:3000 (Santa Cruz Biotechnology)], and protein bands were detected using a chemiluminescent substrate (Pierce) with GeneGnome chemiluminescent detector (Synoptics).

    Nucleic Acid Electrophoresis:

    Article Title: [ 3 H]Dopamine Uptake through the Dopamine and Norepinephrine Transporters is Decreased in the Prefrontal Cortex of Transgenic Mice Expressing HIV-1 Transactivator of Transcription Protein
    Article Snippet: .. Samples were separated by 10% SDS-polyacrylamide gel electrophoresis for ∼90 minutes at 125 V. Samples were then transferred to Immobilon-P transfer membranes (0.45-μm pore size; Millipore Co., Bedford, MA) in transfer buffer (50 mM Tris, 250 mM glycine, 3.5 mM SDS) using a Mini Trans-Blot Electrophoretic Transfer Cell (Bio-Rad, Hercules, CA) for 90 minutes at 75 V. The membranes were then incubated with blocking buffer (5% milk powder in PBS containing 0.5% Tween-20) for 1 hour at room temperature, followed by incubation with either goat anti-DAT (C-20 polyclonal antibody, diluted 1:500 in blocking buffer; Santa Cruz) or mouse anti-NET (MAb tech, 05-1 monoclonal antibody, diluted 1:5000 in blocking buffer) overnight at 4°C. .. Transfer membranes were then washed three times with blocking buffer at room temperature, followed by incubation with either anti-goat horseradish peroxidase (catalog number 305-035-045, diluted 1:10,000 in blocking buffer; Jackson Laboratory) or anti-mouse horseradish peroxidase (catalog number 7076S, diluted 1:15,000 in blocking buffer; Cell Signaling) for 1 hour at room temperature.

    Pore Size:

    Article Title: [ 3 H]Dopamine Uptake through the Dopamine and Norepinephrine Transporters is Decreased in the Prefrontal Cortex of Transgenic Mice Expressing HIV-1 Transactivator of Transcription Protein
    Article Snippet: .. Samples were separated by 10% SDS-polyacrylamide gel electrophoresis for ∼90 minutes at 125 V. Samples were then transferred to Immobilon-P transfer membranes (0.45-μm pore size; Millipore Co., Bedford, MA) in transfer buffer (50 mM Tris, 250 mM glycine, 3.5 mM SDS) using a Mini Trans-Blot Electrophoretic Transfer Cell (Bio-Rad, Hercules, CA) for 90 minutes at 75 V. The membranes were then incubated with blocking buffer (5% milk powder in PBS containing 0.5% Tween-20) for 1 hour at room temperature, followed by incubation with either goat anti-DAT (C-20 polyclonal antibody, diluted 1:500 in blocking buffer; Santa Cruz) or mouse anti-NET (MAb tech, 05-1 monoclonal antibody, diluted 1:5000 in blocking buffer) overnight at 4°C. .. Transfer membranes were then washed three times with blocking buffer at room temperature, followed by incubation with either anti-goat horseradish peroxidase (catalog number 305-035-045, diluted 1:10,000 in blocking buffer; Jackson Laboratory) or anti-mouse horseradish peroxidase (catalog number 7076S, diluted 1:15,000 in blocking buffer; Cell Signaling) for 1 hour at room temperature.

    Blocking Assay:

    Article Title: [ 3 H]Dopamine Uptake through the Dopamine and Norepinephrine Transporters is Decreased in the Prefrontal Cortex of Transgenic Mice Expressing HIV-1 Transactivator of Transcription Protein
    Article Snippet: .. Samples were separated by 10% SDS-polyacrylamide gel electrophoresis for ∼90 minutes at 125 V. Samples were then transferred to Immobilon-P transfer membranes (0.45-μm pore size; Millipore Co., Bedford, MA) in transfer buffer (50 mM Tris, 250 mM glycine, 3.5 mM SDS) using a Mini Trans-Blot Electrophoretic Transfer Cell (Bio-Rad, Hercules, CA) for 90 minutes at 75 V. The membranes were then incubated with blocking buffer (5% milk powder in PBS containing 0.5% Tween-20) for 1 hour at room temperature, followed by incubation with either goat anti-DAT (C-20 polyclonal antibody, diluted 1:500 in blocking buffer; Santa Cruz) or mouse anti-NET (MAb tech, 05-1 monoclonal antibody, diluted 1:5000 in blocking buffer) overnight at 4°C. .. Transfer membranes were then washed three times with blocking buffer at room temperature, followed by incubation with either anti-goat horseradish peroxidase (catalog number 305-035-045, diluted 1:10,000 in blocking buffer; Jackson Laboratory) or anti-mouse horseradish peroxidase (catalog number 7076S, diluted 1:15,000 in blocking buffer; Cell Signaling) for 1 hour at room temperature.

    Article Title: Evidence for an Additive Neurorestorative Effect of Simultaneously Administered CDNF and GDNF in Hemiparkinsonian Rats: Implications for Different Mechanism of Action
    Article Snippet: .. After transfer of proteins to a nitrocellulose membrane, the membrane was incubated in 5% BSA for 1.5 h to block unspecific binding and then incubated in the presence of mouse anti-TH (1:5000, MAB 318, Millipore), goat anti-DAT (1:1000, sc2020, Santa Cruz Biotechnology), mouse anti-β-actin (1:2000, A1978, Sigma-Aldrich), rabbit anti-pERK (1:1000, 9101, Cell Signaling), rabbit anti-ERK (1:1000, 9102, Cell Signaling), rabbit anti-pAkt (1:2000, 9271, Cell Signaling), rabbit anti-Akt (1:1000, 9272, Cell Signaling), rabbit anti-p-eukaryotic initiation factor 2α subunit (eIF2α) (1:1000, 3398, Cell Signaling), rabbit anti-eIF2α (1:1000, 9722, Cell Signaling), rabbit anti-GRP78 (1:1000, sc-1051, Santa Cruz Biotechnology), and mouse anti-β-tubuline antibodies at 4°C overnight. .. Membranes were further incubated in horseradish peroxidase-conjugated secondary antibodies [goat anti-mouse 1:2000 (R&D Systems), donkey anti-goat 1:1000 (Santa Cruz Biotechnology), or donkey anti-rabbit 1:3000 (Santa Cruz Biotechnology)], and protein bands were detected using a chemiluminescent substrate (Pierce) with GeneGnome chemiluminescent detector (Synoptics).

    Membrane:

    Article Title: Evidence for an Additive Neurorestorative Effect of Simultaneously Administered CDNF and GDNF in Hemiparkinsonian Rats: Implications for Different Mechanism of Action
    Article Snippet: .. After transfer of proteins to a nitrocellulose membrane, the membrane was incubated in 5% BSA for 1.5 h to block unspecific binding and then incubated in the presence of mouse anti-TH (1:5000, MAB 318, Millipore), goat anti-DAT (1:1000, sc2020, Santa Cruz Biotechnology), mouse anti-β-actin (1:2000, A1978, Sigma-Aldrich), rabbit anti-pERK (1:1000, 9101, Cell Signaling), rabbit anti-ERK (1:1000, 9102, Cell Signaling), rabbit anti-pAkt (1:2000, 9271, Cell Signaling), rabbit anti-Akt (1:1000, 9272, Cell Signaling), rabbit anti-p-eukaryotic initiation factor 2α subunit (eIF2α) (1:1000, 3398, Cell Signaling), rabbit anti-eIF2α (1:1000, 9722, Cell Signaling), rabbit anti-GRP78 (1:1000, sc-1051, Santa Cruz Biotechnology), and mouse anti-β-tubuline antibodies at 4°C overnight. .. Membranes were further incubated in horseradish peroxidase-conjugated secondary antibodies [goat anti-mouse 1:2000 (R&D Systems), donkey anti-goat 1:1000 (Santa Cruz Biotechnology), or donkey anti-rabbit 1:3000 (Santa Cruz Biotechnology)], and protein bands were detected using a chemiluminescent substrate (Pierce) with GeneGnome chemiluminescent detector (Synoptics).

    Binding Assay:

    Article Title: Evidence for an Additive Neurorestorative Effect of Simultaneously Administered CDNF and GDNF in Hemiparkinsonian Rats: Implications for Different Mechanism of Action
    Article Snippet: .. After transfer of proteins to a nitrocellulose membrane, the membrane was incubated in 5% BSA for 1.5 h to block unspecific binding and then incubated in the presence of mouse anti-TH (1:5000, MAB 318, Millipore), goat anti-DAT (1:1000, sc2020, Santa Cruz Biotechnology), mouse anti-β-actin (1:2000, A1978, Sigma-Aldrich), rabbit anti-pERK (1:1000, 9101, Cell Signaling), rabbit anti-ERK (1:1000, 9102, Cell Signaling), rabbit anti-pAkt (1:2000, 9271, Cell Signaling), rabbit anti-Akt (1:1000, 9272, Cell Signaling), rabbit anti-p-eukaryotic initiation factor 2α subunit (eIF2α) (1:1000, 3398, Cell Signaling), rabbit anti-eIF2α (1:1000, 9722, Cell Signaling), rabbit anti-GRP78 (1:1000, sc-1051, Santa Cruz Biotechnology), and mouse anti-β-tubuline antibodies at 4°C overnight. .. Membranes were further incubated in horseradish peroxidase-conjugated secondary antibodies [goat anti-mouse 1:2000 (R&D Systems), donkey anti-goat 1:1000 (Santa Cruz Biotechnology), or donkey anti-rabbit 1:3000 (Santa Cruz Biotechnology)], and protein bands were detected using a chemiluminescent substrate (Pierce) with GeneGnome chemiluminescent detector (Synoptics).



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