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sc 365322  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology sc 365322
    Sc 365322, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sc 365322/product/Santa Cruz Biotechnology
    Average 94 stars, based on 43 article reviews
    sc 365322 - by Bioz Stars, 2026-02
    94/100 stars

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    Santa Cruz Biotechnology sc 365322
    HAS2 expression, and effect of HA coat modulation on NP uptake A. HAS2 expression in 4 different breast cancer cell lines measured by qRT-PCR. Relative quantification was calculated with HMLE-E sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. B. <t>HAS3</t> expression in 4 different breast cancer cell lines, measured by qRT-PCR. Relative quantification was calculated with HMLE-M sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. For A and B, t he statistical significance was determined by using the one-way Anova test, with a Sidak’s multiple comparison test. Note: ns, non-significant; * p < 0.05, ** p <0.005 and **** p < 0.0001. C. Representative images of hyaluronic acid staining in the 4 different cell lines. Nuclei were stained with Hoescht (blue) and HA Binding proteins coupled to biotin were further detected using streptavidin-FITC (green). Images were obtained by confocal microscopy. Scale bar is 10µm. D. Mean Fluorescence Intensity of HABP from at least 10000 cells for each of the 4 indicated cell lines, analysed by flow cytometry. Analysis was performed in triplicates. E. SSC-A deviation signals from T47D and MDA-MB231 cells treated with hyaluronidase and exposed to NM100 or NM103 TiO2 NPs. The graph represents the mean of data from 10000 cells, and in duplicates. The statistical analysis comparing untreated vs treated cells was performed with one-way anova. Ns=non significant, *indicates a p-value<0,05 and **indicates a p-value<0,01.
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    Image Search Results


    HAS2 expression, and effect of HA coat modulation on NP uptake A. HAS2 expression in 4 different breast cancer cell lines measured by qRT-PCR. Relative quantification was calculated with HMLE-E sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. B. HAS3 expression in 4 different breast cancer cell lines, measured by qRT-PCR. Relative quantification was calculated with HMLE-M sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. For A and B, t he statistical significance was determined by using the one-way Anova test, with a Sidak’s multiple comparison test. Note: ns, non-significant; * p < 0.05, ** p <0.005 and **** p < 0.0001. C. Representative images of hyaluronic acid staining in the 4 different cell lines. Nuclei were stained with Hoescht (blue) and HA Binding proteins coupled to biotin were further detected using streptavidin-FITC (green). Images were obtained by confocal microscopy. Scale bar is 10µm. D. Mean Fluorescence Intensity of HABP from at least 10000 cells for each of the 4 indicated cell lines, analysed by flow cytometry. Analysis was performed in triplicates. E. SSC-A deviation signals from T47D and MDA-MB231 cells treated with hyaluronidase and exposed to NM100 or NM103 TiO2 NPs. The graph represents the mean of data from 10000 cells, and in duplicates. The statistical analysis comparing untreated vs treated cells was performed with one-way anova. Ns=non significant, *indicates a p-value<0,05 and **indicates a p-value<0,01.

    Journal: bioRxiv

    Article Title: The uptake of metallic nanoparticles in breast cancer cell lines is modulated by the HA-CD44 axis

    doi: 10.1101/2025.02.12.637873

    Figure Lengend Snippet: HAS2 expression, and effect of HA coat modulation on NP uptake A. HAS2 expression in 4 different breast cancer cell lines measured by qRT-PCR. Relative quantification was calculated with HMLE-E sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. B. HAS3 expression in 4 different breast cancer cell lines, measured by qRT-PCR. Relative quantification was calculated with HMLE-M sample as a reference. Measures of expression were performed in triplicates, and error bars represent RQ min and RQ max values. For A and B, t he statistical significance was determined by using the one-way Anova test, with a Sidak’s multiple comparison test. Note: ns, non-significant; * p < 0.05, ** p <0.005 and **** p < 0.0001. C. Representative images of hyaluronic acid staining in the 4 different cell lines. Nuclei were stained with Hoescht (blue) and HA Binding proteins coupled to biotin were further detected using streptavidin-FITC (green). Images were obtained by confocal microscopy. Scale bar is 10µm. D. Mean Fluorescence Intensity of HABP from at least 10000 cells for each of the 4 indicated cell lines, analysed by flow cytometry. Analysis was performed in triplicates. E. SSC-A deviation signals from T47D and MDA-MB231 cells treated with hyaluronidase and exposed to NM100 or NM103 TiO2 NPs. The graph represents the mean of data from 10000 cells, and in duplicates. The statistical analysis comparing untreated vs treated cells was performed with one-way anova. Ns=non significant, *indicates a p-value<0,05 and **indicates a p-value<0,01.

    Article Snippet: The references of the Taqman probe sets used are as follows : GAPDH : Hs99999905_m1, CD44v2-10 : Hs01075866_m1, CD44s : Hs01081473_m1, HAS2 : Hs00193435_m1, HAS3 : Hs00193436_m1.

    Techniques: Expressing, Quantitative RT-PCR, Quantitative Proteomics, Comparison, Staining, Binding Assay, Confocal Microscopy, Fluorescence, Flow Cytometry

    Primer sequences used for quantification of gene expression.

    Journal: Molecular Medicine Reports

    Article Title: Effects of natural killer cell‑conditioned medium on UVB‑induced photoaging in human keratinocytes and a human reconstructed skin model

    doi: 10.3892/mmr.2025.13488

    Figure Lengend Snippet: Primer sequences used for quantification of gene expression.

    Article Snippet: Anti-hyaluronan synthase3 , 1:5,000 , sc-365322 , Santa Cruz Biotechnology, Inc..

    Techniques: Expressing, Sequencing

    Antibodies used for western blot analysis.

    Journal: Molecular Medicine Reports

    Article Title: Effects of natural killer cell‑conditioned medium on UVB‑induced photoaging in human keratinocytes and a human reconstructed skin model

    doi: 10.3892/mmr.2025.13488

    Figure Lengend Snippet: Antibodies used for western blot analysis.

    Article Snippet: Anti-hyaluronan synthase3 , 1:5,000 , sc-365322 , Santa Cruz Biotechnology, Inc..

    Techniques: Western Blot