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prostate specific antigen psa  (Elabscience Biotechnology)


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    Elabscience Biotechnology prostate specific antigen psa
    Prostate Specific Antigen Psa, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+psa+elisa+kit/pmc12905635-177-3-14?v=Elabscience+Biotechnology
    Average 94 stars, based on 8 article reviews
    prostate specific antigen psa - by Bioz Stars, 2026-07
    94/100 stars

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    prostate specific antigen psa  (Elabscience Biotechnology)
    94
    Elabscience Biotechnology prostate specific antigen psa
    Prostate Specific Antigen Psa, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+psa+elisa+kit/pmc12905635-177-3-14?v=Elabscience+Biotechnology
    Average 94 stars, based on 1 article reviews
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    mouse psa elisa kit  (Elabscience Biotechnology)
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    <t>PSA</t> plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by <t>ELISA</t> at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.
    Mouse Psa Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mouse psa elisa kit - by Bioz Stars, 2026-07
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    <t>PSA</t> plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by <t>ELISA</t> at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.
    Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    e el m0961  (Elabscience Biotechnology)
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    Elabscience Biotechnology e el m0961
    <t>PSA</t> plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by <t>ELISA</t> at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.
    E El M0961, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    mouse psa  (Elabscience Biotechnology)
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    <t>PSA</t> plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by <t>ELISA</t> at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.
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    mouse specific kits  (Cusabio)
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    <t>PSA</t> plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by <t>ELISA</t> at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.
    Mouse Specific Kits, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+psa+elisa+kit/pm32171969-115-9-16?v=Cusabio
    Average 93 stars, based on 1 article reviews
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    PSA plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by ELISA at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.

    Journal: International Journal of Biological Sciences

    Article Title: TRPV1 Downregulation Impairs Prostate Cancer Growth: Functional and Translational Insights from Cellular and In Vivo Models

    doi: 10.7150/ijbs.125429

    Figure Lengend Snippet: PSA plasma levels and TRPV1 expression in the prostates of TRAMP mice fed different diets. (A) PSA levels in plasma measured by ELISA at the end of the experiment. Results are expressed as mean ± SD (n = 6 per group) along with median values. p -values comparing each group to the STD group are shown in the rightmost column. (B) Left: TRPV1 mRNA levels determined by RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). Right: TRPV1 protein levels assessed by Western blotting with β-actin used as a loading control. A representative blot from two independent samples per group is shown. Densitometric values (mean ± SD) relative to the STD group are presented. (C) Protein levels of PCNA and Cyclin B1, key regulators of proliferation and the cell cycle, analyzed via Western blotting. A representative blot from two samples per group is shown with densitometric values (mean ± SD) relative to the STD group. (D) Relative mRNA expression levels of the stemness markers Oct4 and Nanog in prostate tissues from TRAMP mice. mRNA levels were quantified via RT-qPCR, normalized to GAPDH (housekeeping gene) and presented as mean ± SD (n = 6 per group). (E) Correlation analysis between TRPV1 and the stemness markers Oct4 and Nanog in prostate tissues of TRAMP mice. Top: Scatter plots showing Pearson's correlation coefficients (r) for TRPV1 vs. Oct4 and TRPV1 vs. Nanog. Bottom: Heatmap displaying Pearson's correlation coefficients for TRPV1, Oct4, and Nanog expression. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***) and p < 0.0001 (****) indicate significant differences via one-way ANOVA.

    Article Snippet: Plasma levels of prostate-specific antigen (PSA) were measured using a Mouse PSA ELISA Kit (Elabscience®, Houston, TX, USA; catalogue number: E-EL-M0961), following the manufacturer's instructions.

    Techniques: Clinical Proteomics, Expressing, Enzyme-linked Immunosorbent Assay, Quantitative RT-PCR, Western Blot, Control