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rat ctx i elisa kit  (Elabscience Biotechnology)


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    Elabscience Biotechnology rat ctx i elisa kit
    Rat Ctx I Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rat+ctx+i+elisa+kit/pmc13057037-331-24-30?v=Elabscience+Biotechnology
    Average 93 stars, based on 21 article reviews
    rat ctx i elisa kit - by Bioz Stars, 2026-08
    93/100 stars

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    Darolutamide in combination with radium-223 inhibits abnormal bone turnover. The levels of the bone formation marker ( A , B ) <t>PINP</t> and bone resorption marker ( C , D ) CTX-I were measured in blood samples collected from the saphenous vein of mice ( n = 7–9/group) 2 days prior to and 13, 27, and 41 days after the initiation of treatment. The mice were treated with vehicle; darolutamide (100 mg/kg, BID, p.o.); radium-223 (330 kBq/kg, Q4Wx2, i.v.); or a combination of darolutamide and radium-223 and were sacrificed on day 41 after the start of treatment, except for one mouse in the radium-223 monotherapy group, which was sacrificed on day 38. Plots describe mean and standard deviation (SD). Statistical analyses were performed using mixed models and model contrasts ( A , C ), ANOVA followed by contrasts ( B ), or a Kruskal–Wallis test followed by Dunn’s pairwise comparison test ( D ): *, p < 0.05; **, p < 0.01; ***, p < 0.001.
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    Darolutamide in combination with radium-223 inhibits abnormal bone turnover. The levels of the bone formation marker ( A , B ) PINP and bone resorption marker ( C , D ) CTX-I were measured in blood samples collected from the saphenous vein of mice ( n = 7–9/group) 2 days prior to and 13, 27, and 41 days after the initiation of treatment. The mice were treated with vehicle; darolutamide (100 mg/kg, BID, p.o.); radium-223 (330 kBq/kg, Q4Wx2, i.v.); or a combination of darolutamide and radium-223 and were sacrificed on day 41 after the start of treatment, except for one mouse in the radium-223 monotherapy group, which was sacrificed on day 38. Plots describe mean and standard deviation (SD). Statistical analyses were performed using mixed models and model contrasts ( A , C ), ANOVA followed by contrasts ( B ), or a Kruskal–Wallis test followed by Dunn’s pairwise comparison test ( D ): *, p < 0.05; **, p < 0.01; ***, p < 0.001.

    Journal: International Journal of Molecular Sciences

    Article Title: Darolutamide in Combination with Radium-223 Exhibits Synergistic Antitumor Efficacy in LNCaP Prostate Cancer Models

    doi: 10.3390/ijms252413672

    Figure Lengend Snippet: Darolutamide in combination with radium-223 inhibits abnormal bone turnover. The levels of the bone formation marker ( A , B ) PINP and bone resorption marker ( C , D ) CTX-I were measured in blood samples collected from the saphenous vein of mice ( n = 7–9/group) 2 days prior to and 13, 27, and 41 days after the initiation of treatment. The mice were treated with vehicle; darolutamide (100 mg/kg, BID, p.o.); radium-223 (330 kBq/kg, Q4Wx2, i.v.); or a combination of darolutamide and radium-223 and were sacrificed on day 41 after the start of treatment, except for one mouse in the radium-223 monotherapy group, which was sacrificed on day 38. Plots describe mean and standard deviation (SD). Statistical analyses were performed using mixed models and model contrasts ( A , C ), ANOVA followed by contrasts ( B ), or a Kruskal–Wallis test followed by Dunn’s pairwise comparison test ( D ): *, p < 0.05; **, p < 0.01; ***, p < 0.001.

    Article Snippet: The markers were analyzed using a Human Kallikrein 3/PSA Quantikine ® enzyme-linked immunosorbent assay (ELISA) kit (R&D Systems, Minneapolis, MN, USA) and Rat/Mouse PINP and RatLaps™ CTX-I ELISA kits (both from IDS Ltd., Boldon, UK).

    Techniques: Marker, Standard Deviation, Comparison