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primary antibodies to lamp3  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc primary antibodies to lamp3
    Primary Antibodies To Lamp3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+antibodies+to+lamp3/pm41651377-251-0-4?v=Cell+Signaling+Technology+Inc
    Average 86 stars, based on 1 article reviews
    primary antibodies to lamp3 - by Bioz Stars, 2026-07
    86/100 stars

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    Free cholesterol accumulates in the late endosome/lysosome compartment in ALS muscle . Intracellular distribution of free cholesterol on transversal slices of deltoid muscle biopsies from amyotrophic lateral sclerosis (ALS) and controls (CTRL) (representative image). Lysosomes were labelled by immunofluorescence directed against <t>LAMP3,</t> unesterified cholesterol was stained with filipin and nuclei were stained by propidium iodide (PI). Scale bar = 50 µm. Arrows in the left panels indicate co-localizations between the cholesterol and LAMP3 and arrows in the right panels indicate lysosome without cholesterol co-localization.
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    Free cholesterol accumulates in the late endosome/lysosome compartment in ALS muscle . Intracellular distribution of free cholesterol on transversal slices of deltoid muscle biopsies from amyotrophic lateral sclerosis (ALS) and controls (CTRL) (representative image). Lysosomes were labelled by immunofluorescence directed against <t>LAMP3,</t> unesterified cholesterol was stained with filipin and nuclei were stained by propidium iodide (PI). Scale bar = 50 µm. Arrows in the left panels indicate co-localizations between the cholesterol and LAMP3 and arrows in the right panels indicate lysosome without cholesterol co-localization.
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    (A) ILP increases NO release. NO production as assessed by DAF-fluorescence doubled in ECs exposed to 1% ILP for 2 hours. Concomitant incubation with L-NAME not only prevented this increase but brought it below control levels; * P < 0.05 vs control, † P < 0.05 vs ILP. (B) ILP increases formation of endosomes: <t>CD63/LAMP3</t> fluorescence with ILP shows increased number of endosomes within the cell when compared to no ILP treatment; * P < 0.05 vs control.
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    Santa Cruz Biotechnology cd63/lamp3 primary antibody sc-5275
    (A) ILP increases NO release. NO production as assessed by DAF-fluorescence doubled in ECs exposed to 1% ILP for 2 hours. Concomitant incubation with L-NAME not only prevented this increase but brought it below control levels; * P < 0.05 vs control, † P < 0.05 vs ILP. (B) ILP increases formation of endosomes: <t>CD63/LAMP3</t> fluorescence with ILP shows increased number of endosomes within the cell when compared to no ILP treatment; * P < 0.05 vs control.
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    Image Search Results


    Free cholesterol accumulates in the late endosome/lysosome compartment in ALS muscle . Intracellular distribution of free cholesterol on transversal slices of deltoid muscle biopsies from amyotrophic lateral sclerosis (ALS) and controls (CTRL) (representative image). Lysosomes were labelled by immunofluorescence directed against LAMP3, unesterified cholesterol was stained with filipin and nuclei were stained by propidium iodide (PI). Scale bar = 50 µm. Arrows in the left panels indicate co-localizations between the cholesterol and LAMP3 and arrows in the right panels indicate lysosome without cholesterol co-localization.

    Journal: Brain

    Article Title: Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosis

    doi: 10.1093/brain/awae270

    Figure Lengend Snippet: Free cholesterol accumulates in the late endosome/lysosome compartment in ALS muscle . Intracellular distribution of free cholesterol on transversal slices of deltoid muscle biopsies from amyotrophic lateral sclerosis (ALS) and controls (CTRL) (representative image). Lysosomes were labelled by immunofluorescence directed against LAMP3, unesterified cholesterol was stained with filipin and nuclei were stained by propidium iodide (PI). Scale bar = 50 µm. Arrows in the left panels indicate co-localizations between the cholesterol and LAMP3 and arrows in the right panels indicate lysosome without cholesterol co-localization.

    Article Snippet: Slides were incubated with mouse monoclonal anti-CD63 (LAMP3) primary antibody (1:100, H5C6, DSHB) diluted in a solution of 0.05% saponin and 10% donkey serum in PBS overnight at 4°C.

    Techniques: Immunofluorescence, Staining

    High-power (40×) view showing LAMP3 expression.

    Journal: Cureus

    Article Title: Lysosome-Associated Membrane Protein-3 (LAMP3) Expression in Oral Squamous Cell Carcinoma and Its Relationship With Clinicopathological Parameters: A Cross-Sectional Study

    doi: 10.7759/cureus.69790

    Figure Lengend Snippet: High-power (40×) view showing LAMP3 expression.

    Article Snippet: The tissues were then blocked for endogenous peroxidase activity with pre-diluted 3% hydrogen peroxide, and incubated with 1:200 dilution of anti-LAMP3 mouse monoclonal primary antibody (anti-LAMP3, clone 16H11.2, Merck Millipore, Germany).

    Techniques: Expressing

    Relationship of  LAMP3  expression with clinicopathological parameters in oral squamous cell carcinoma. *: p-value <0.05* = Statistically significant; **: p-value <0.001 = highly significant.

    Journal: Cureus

    Article Title: Lysosome-Associated Membrane Protein-3 (LAMP3) Expression in Oral Squamous Cell Carcinoma and Its Relationship With Clinicopathological Parameters: A Cross-Sectional Study

    doi: 10.7759/cureus.69790

    Figure Lengend Snippet: Relationship of LAMP3 expression with clinicopathological parameters in oral squamous cell carcinoma. *: p-value <0.05* = Statistically significant; **: p-value <0.001 = highly significant.

    Article Snippet: The tissues were then blocked for endogenous peroxidase activity with pre-diluted 3% hydrogen peroxide, and incubated with 1:200 dilution of anti-LAMP3 mouse monoclonal primary antibody (anti-LAMP3, clone 16H11.2, Merck Millipore, Germany).

    Techniques: Expressing

    (A) ILP increases NO release. NO production as assessed by DAF-fluorescence doubled in ECs exposed to 1% ILP for 2 hours. Concomitant incubation with L-NAME not only prevented this increase but brought it below control levels; * P < 0.05 vs control, † P < 0.05 vs ILP. (B) ILP increases formation of endosomes: CD63/LAMP3 fluorescence with ILP shows increased number of endosomes within the cell when compared to no ILP treatment; * P < 0.05 vs control.

    Journal: JPEN. Journal of parenteral and enteral nutrition

    Article Title: Intralipid™ Increases Nitric Oxide Release from Human Endothelial Cells during Oxidative Stress

    doi: 10.1002/jpen.1834

    Figure Lengend Snippet: (A) ILP increases NO release. NO production as assessed by DAF-fluorescence doubled in ECs exposed to 1% ILP for 2 hours. Concomitant incubation with L-NAME not only prevented this increase but brought it below control levels; * P < 0.05 vs control, † P < 0.05 vs ILP. (B) ILP increases formation of endosomes: CD63/LAMP3 fluorescence with ILP shows increased number of endosomes within the cell when compared to no ILP treatment; * P < 0.05 vs control.

    Article Snippet: A 30-minute incubation at 37°C with the CD63/LAMP3 primary antibody (1:50, sc-5275, Santa Cruz Biotechnologies Inc.) was followed by three washes with PBS for 5 minutes each.

    Techniques: Fluorescence, Incubation