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human p1np elisa kit  (Elabscience Biotechnology)


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    Elabscience Biotechnology human p1np elisa kit
    Human P1np Elisa Kit, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 85 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+p1np+elisa+kit/Human+Testosterone+ELISA+Kit/pmc12735629-139-5-9
    Average 94 stars, based on 85 article reviews
    human p1np elisa kit - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Effects of Greek Yogurt Supplementation and Exercise on Markers of Bone Turnover and Inflammation in Older Adult Exercisers: An 8-Week Pilot Intervention Trial
    Article Snippet: The analyses of amino-terminal propeptide of type I collagen (P1NP) and C -telopeptides of type I collagen (CTX-I) were performed on a PerkinElmer EnSpireTM 2300 Multilabel Reader System (Waltham, MA, USA). .. P1NP was measured using the Human P1NP ELISA Kit (Elabscience Biotechnology Inc., Houston, TX, USA) with assay sensitivity of 9.38 pg/mL and an intra- and inter-assay coefficient of variation (%CV) < 10 and <15, respectively. .. CTX-I was measured using the Human CTX ELISA Kit (Elabscience Biotechnology Inc., Houston, TX, USA) with assay sensitivity of 0.09 ng/mL and an intra- and inter-assay %CV < 10 and <15, respectively.

    Inter Assay:

    Article Title: Effects of Greek Yogurt Supplementation and Exercise on Markers of Bone Turnover and Inflammation in Older Adult Exercisers: An 8-Week Pilot Intervention Trial
    Article Snippet: The analyses of amino-terminal propeptide of type I collagen (P1NP) and C -telopeptides of type I collagen (CTX-I) were performed on a PerkinElmer EnSpireTM 2300 Multilabel Reader System (Waltham, MA, USA). .. P1NP was measured using the Human P1NP ELISA Kit (Elabscience Biotechnology Inc., Houston, TX, USA) with assay sensitivity of 9.38 pg/mL and an intra- and inter-assay coefficient of variation (%CV) < 10 and <15, respectively. .. CTX-I was measured using the Human CTX ELISA Kit (Elabscience Biotechnology Inc., Houston, TX, USA) with assay sensitivity of 0.09 ng/mL and an intra- and inter-assay %CV < 10 and <15, respectively.



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    FIGURE 1 Plasma bone markers in radiographic and non-radiographic axial SpA patients, and controls. The circulating levels of (A) <t>procollagen</t> type I N- terminal propeptide <t>(P1NP),</t> indicative of osteoblast activity, (B) tartrate-resistant acid phosphatase 5b (TRACP5b), and (C) receptor activator of nuclear factor kappa-B ligand (RANKL), both markers of osteoclast activity, were measured. Additionally, levels of (D) osteoprotegerin (OPG), a RANKL decoy receptor that inhibits osteoclast function, (E) RANKL/OPG ratio, and (F) Sclerostin, an inhibitor of Wnt signaling that modulates bone formation, were also analyzed. Bars represent mean ± standard deviation. Significant differences: *p < 0.05; **p < 0.01.
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    FIGURE 1 Plasma bone markers in radiographic and non-radiographic axial SpA patients, and controls. The circulating levels of (A) <t>procollagen</t> type I N- terminal propeptide <t>(P1NP),</t> indicative of osteoblast activity, (B) tartrate-resistant acid phosphatase 5b (TRACP5b), and (C) receptor activator of nuclear factor kappa-B ligand (RANKL), both markers of osteoclast activity, were measured. Additionally, levels of (D) osteoprotegerin (OPG), a RANKL decoy receptor that inhibits osteoclast function, (E) RANKL/OPG ratio, and (F) Sclerostin, an inhibitor of Wnt signaling that modulates bone formation, were also analyzed. Bars represent mean ± standard deviation. Significant differences: *p < 0.05; **p < 0.01.
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    Figure 1. Fat percentage and bone turnover enzymes across VD deficiency categories. (A) Repre- sentative images of DEXA-measured body composition. Graphical representations of total fat % (B) and VAT mass (C) across VD deficiency groups. Serum levels of CTX (D) and <t>P1NP</t> (E) measured by ELISA assays. Results are represented as means ± standard error (SE). A significant p-value is denoted by * for the comparison between the mild and moderate deficiency groups, # for the comparison between the mild and severe deficiency groups, and † for the comparison between moderate and severe deficiency groups.
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    Image Search Results


    FIGURE 1 Plasma bone markers in radiographic and non-radiographic axial SpA patients, and controls. The circulating levels of (A) procollagen type I N- terminal propeptide (P1NP), indicative of osteoblast activity, (B) tartrate-resistant acid phosphatase 5b (TRACP5b), and (C) receptor activator of nuclear factor kappa-B ligand (RANKL), both markers of osteoclast activity, were measured. Additionally, levels of (D) osteoprotegerin (OPG), a RANKL decoy receptor that inhibits osteoclast function, (E) RANKL/OPG ratio, and (F) Sclerostin, an inhibitor of Wnt signaling that modulates bone formation, were also analyzed. Bars represent mean ± standard deviation. Significant differences: *p < 0.05; **p < 0.01.

    Journal: Frontiers in endocrinology

    Article Title: Bone metabolism and inflammatory biomarkers in radiographic and non-radiographic axial spondyloarthritis patients: a comprehensive evaluation.

    doi: 10.3389/fendo.2024.1227196

    Figure Lengend Snippet: FIGURE 1 Plasma bone markers in radiographic and non-radiographic axial SpA patients, and controls. The circulating levels of (A) procollagen type I N- terminal propeptide (P1NP), indicative of osteoblast activity, (B) tartrate-resistant acid phosphatase 5b (TRACP5b), and (C) receptor activator of nuclear factor kappa-B ligand (RANKL), both markers of osteoclast activity, were measured. Additionally, levels of (D) osteoprotegerin (OPG), a RANKL decoy receptor that inhibits osteoclast function, (E) RANKL/OPG ratio, and (F) Sclerostin, an inhibitor of Wnt signaling that modulates bone formation, were also analyzed. Bars represent mean ± standard deviation. Significant differences: *p < 0.05; **p < 0.01.

    Article Snippet: Markers related to bone remodeling To estimate the osteoblastic activity, also referred to as bone formation, human procollagen type 1 N-terminal propeptide (P1NP) quantification was carried out in plasma samples (1:200 dilution) using a commercial ELISA Kit (Cusabio Technology LLC, Houston, TX, USA) following the manufacturer’s instructions.

    Techniques: Clinical Proteomics, Activity Assay, Standard Deviation

    FIGURE 5 ROC curve analyses of circulating levels of inflammatory-related proteins and bone turnover markers as potential biomarkers of disease in axSpA. (A) Positive relation of inflammatory-related proteins in r-axSpA patients compared with controls [IL6 (AUC 0.78; p = 0.001), OSM (AUC 0.72; p = 0.011), and TNFRSF9 (AUC 0.73; p = 0.006)]. (B) Negative relation in P1NP in r-axSpA patients compared to controls (AUC 0.75; p = 0.003). (C) Positive relation in IL13 in nr-axSpA patients compared to controls (AUC 0.71; p = 0.065). (D) Positive relation in IL13 in nr-axSpA patients compared to r-axSpA patients (AUC 0.63; p = 0.198). Significant differences **p < 0.01.

    Journal: Frontiers in endocrinology

    Article Title: Bone metabolism and inflammatory biomarkers in radiographic and non-radiographic axial spondyloarthritis patients: a comprehensive evaluation.

    doi: 10.3389/fendo.2024.1227196

    Figure Lengend Snippet: FIGURE 5 ROC curve analyses of circulating levels of inflammatory-related proteins and bone turnover markers as potential biomarkers of disease in axSpA. (A) Positive relation of inflammatory-related proteins in r-axSpA patients compared with controls [IL6 (AUC 0.78; p = 0.001), OSM (AUC 0.72; p = 0.011), and TNFRSF9 (AUC 0.73; p = 0.006)]. (B) Negative relation in P1NP in r-axSpA patients compared to controls (AUC 0.75; p = 0.003). (C) Positive relation in IL13 in nr-axSpA patients compared to controls (AUC 0.71; p = 0.065). (D) Positive relation in IL13 in nr-axSpA patients compared to r-axSpA patients (AUC 0.63; p = 0.198). Significant differences **p < 0.01.

    Article Snippet: Markers related to bone remodeling To estimate the osteoblastic activity, also referred to as bone formation, human procollagen type 1 N-terminal propeptide (P1NP) quantification was carried out in plasma samples (1:200 dilution) using a commercial ELISA Kit (Cusabio Technology LLC, Houston, TX, USA) following the manufacturer’s instructions.

    Techniques:

    Figure 1. Fat percentage and bone turnover enzymes across VD deficiency categories. (A) Repre- sentative images of DEXA-measured body composition. Graphical representations of total fat % (B) and VAT mass (C) across VD deficiency groups. Serum levels of CTX (D) and P1NP (E) measured by ELISA assays. Results are represented as means ± standard error (SE). A significant p-value is denoted by * for the comparison between the mild and moderate deficiency groups, # for the comparison between the mild and severe deficiency groups, and † for the comparison between moderate and severe deficiency groups.

    Journal: International journal of molecular sciences

    Article Title: Obesity-Associated Vitamin D Deficiency Correlates with Adipose Tissue DNA Hypomethylation, Inflammation, and Vascular Dysfunction.

    doi: 10.3390/ijms232214377

    Figure Lengend Snippet: Figure 1. Fat percentage and bone turnover enzymes across VD deficiency categories. (A) Repre- sentative images of DEXA-measured body composition. Graphical representations of total fat % (B) and VAT mass (C) across VD deficiency groups. Serum levels of CTX (D) and P1NP (E) measured by ELISA assays. Results are represented as means ± standard error (SE). A significant p-value is denoted by * for the comparison between the mild and moderate deficiency groups, # for the comparison between the mild and severe deficiency groups, and † for the comparison between moderate and severe deficiency groups.

    Article Snippet: Human C-terminal cross-linking telopeptide of type I (CTX-1) and human procollagen type 1 N-terminal propeptide (P1NP) ELISA Kits (Novus Biologicals, Centennial, CO, USA) were used to measure plasma levels of CTX1 and P1NP.

    Techniques: Enzyme-linked Immunosorbent Assay, Comparison