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ctx 1 elisa kit  (Cusabio)


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    Cusabio ctx 1 elisa kit
    Ctx 1 Elisa Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ctx+1/pmc12757577-45-0-4?v=Cusabio
    Average 93 stars, based on 22 article reviews
    ctx 1 elisa kit - by Bioz Stars, 2026-07
    93/100 stars

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    Cxcr2 deletion expands the detected pro-inflammatory cytokines and alters systemic bone turnover. a Log-2 transformed fold change in cytokine expression (KO/WT) in Cxcr2 WT versus KO serum, quantified by Eve Technologies 32-Plex Cytokine Array. N = 6 mice per genotype. b Serum concentration of G-CSF and CXCL5 in Cxcr2 WT and KO mice. N = 3–8 mice per genotype. c Serum concentration of osteoblast and osteoclast activity markers P1NP <t>and</t> <t>CTX-1</t> in Cxcr2 WT and KO mice. N = 4–5 mice per genotype. d Concentration of RANKL and OPG and OPG/RANKL ratio in Cxcr2 WT and KO bone conditioned media. N = 8 samples per group. Error bars represent standard deviation. Analysis of Cxcr2 WT versus KO using Welch’s t- test. Significance levels for differences are indicated: * p < 0.05, ** p < 0.01, *** p < 0.001, ns: not significant ( p ≥ 0.05). N = 4–6 mice per group
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    Image Search Results


    Cxcr2 deletion expands the detected pro-inflammatory cytokines and alters systemic bone turnover. a Log-2 transformed fold change in cytokine expression (KO/WT) in Cxcr2 WT versus KO serum, quantified by Eve Technologies 32-Plex Cytokine Array. N = 6 mice per genotype. b Serum concentration of G-CSF and CXCL5 in Cxcr2 WT and KO mice. N = 3–8 mice per genotype. c Serum concentration of osteoblast and osteoclast activity markers P1NP and CTX-1 in Cxcr2 WT and KO mice. N = 4–5 mice per genotype. d Concentration of RANKL and OPG and OPG/RANKL ratio in Cxcr2 WT and KO bone conditioned media. N = 8 samples per group. Error bars represent standard deviation. Analysis of Cxcr2 WT versus KO using Welch’s t- test. Significance levels for differences are indicated: * p < 0.05, ** p < 0.01, *** p < 0.001, ns: not significant ( p ≥ 0.05). N = 4–6 mice per group

    Journal: Calcified Tissue International

    Article Title: Cxcr2 is Required for Osteoclast Regulation, Bone Structure, and Hematological Response During Bone (Re)modeling

    doi: 10.1007/s00223-025-01470-x

    Figure Lengend Snippet: Cxcr2 deletion expands the detected pro-inflammatory cytokines and alters systemic bone turnover. a Log-2 transformed fold change in cytokine expression (KO/WT) in Cxcr2 WT versus KO serum, quantified by Eve Technologies 32-Plex Cytokine Array. N = 6 mice per genotype. b Serum concentration of G-CSF and CXCL5 in Cxcr2 WT and KO mice. N = 3–8 mice per genotype. c Serum concentration of osteoblast and osteoclast activity markers P1NP and CTX-1 in Cxcr2 WT and KO mice. N = 4–5 mice per genotype. d Concentration of RANKL and OPG and OPG/RANKL ratio in Cxcr2 WT and KO bone conditioned media. N = 8 samples per group. Error bars represent standard deviation. Analysis of Cxcr2 WT versus KO using Welch’s t- test. Significance levels for differences are indicated: * p < 0.05, ** p < 0.01, *** p < 0.001, ns: not significant ( p ≥ 0.05). N = 4–6 mice per group

    Article Snippet: Levels of CTX-1 and P1NP were measured using the Serum Crosslaps (CTX-1) ELISA (Immunodiagnostic Systems #AC-02F1) and Rat/Mouse P1NP ELISA (Immunodiagnostic Systems #AC-33F1) according to the manufacturer’s protocols.

    Techniques: Transformation Assay, Expressing, Concentration Assay, Activity Assay, Standard Deviation