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type i collagen  (Cusabio)


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    Cusabio type i collagen
    Type I Collagen, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/type+i+collagen+c+telopeptide/Mouse+cross+linked+C-telopeptide+of+type+I+collagen+(CTX-%E2%85%A0)+ELISA+Kit/pm41242268-101-17-22
    Average 93 stars, based on 27 article reviews
    type i collagen - by Bioz Stars, 2026-09
    93/100 stars

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    Animal Model:

    Article Title: Cervical vertebrae for early bone loss evaluation in osteoporosis mouse models.
    Article Snippet: .. We have tested the serum estradiol and testosterone levels to characterize the animal model. Then, the measurement of biochemical markers of bone turnover in serum including propeptide of type I procollagen (PINP, CSB-E12775m, CUSABIO, China), osteocalcin (OCN, CSB-E06917m, CUSABIO, China) and type I collagen C-telopeptide (CTX, CSBE12782m, CUSABIO, China) to evaluate the process of OP with group information were blinded to assessors. ..



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    Immune profile of WT and CD5L⁻ mice during CIA. A Serum CD5L levels measured in WT mice after immunization. p -values were obtained using the Kruskal–Wallis test with Dunn’s multiple comparisons. B Frequencies of blood leukocyte subsets in WT ( n = 10) and CD5L⁻ ( n = 10) mice. Leukocytes were phenotyped by flow cytometry: CD11b + cells, monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺); inflammatory monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁺); and Ly6C⁻ monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁻). Shaded area indicates mean and SEM of total leukocyte frequency. p -values were calculated using Šídák’s multiple-comparisons test. C Serum cytokine levels in WT ( n = 6) and CD5L⁻ ( n = 6) mice. p -values were calculated using the Mann–Whitney test. D Serum RANKL and <t>cross-linked</t> <t>C-telopeptide</t> of <t>type</t> <t>I</t> collagen <t>(CTX-I)</t> levels on day 56 after immunization. p -values were obtained using an unpaired t -test with Welch’s correction. E Splenic gene expression in non-immunized WT ( n = 5) and CD5L⁻ ( n = 5) mice, measured by RT-qPCR and normalized to Actb (β-actin). p -values were calculated using a two-tailed unpaired t -test with Welch’s correction
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    Immune profile of WT and CD5L⁻ mice during CIA. A Serum CD5L levels measured in WT mice after immunization. p -values were obtained using the Kruskal–Wallis test with Dunn’s multiple comparisons. B Frequencies of blood leukocyte subsets in WT ( n = 10) and CD5L⁻ ( n = 10) mice. Leukocytes were phenotyped by flow cytometry: CD11b + cells, monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺); inflammatory monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁺); and Ly6C⁻ monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁻). Shaded area indicates mean and SEM of total leukocyte frequency. p -values were calculated using Šídák’s multiple-comparisons test. C Serum cytokine levels in WT ( n = 6) and CD5L⁻ ( n = 6) mice. p -values were calculated using the Mann–Whitney test. D Serum RANKL and <t>cross-linked</t> <t>C-telopeptide</t> of <t>type</t> <t>I</t> collagen <t>(CTX-I)</t> levels on day 56 after immunization. p -values were obtained using an unpaired t -test with Welch’s correction. E Splenic gene expression in non-immunized WT ( n = 5) and CD5L⁻ ( n = 5) mice, measured by RT-qPCR and normalized to Actb (β-actin). p -values were calculated using a two-tailed unpaired t -test with Welch’s correction
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    Immune profile of WT and CD5L⁻ mice during CIA. A Serum CD5L levels measured in WT mice after immunization. p -values were obtained using the Kruskal–Wallis test with Dunn’s multiple comparisons. B Frequencies of blood leukocyte subsets in WT ( n = 10) and CD5L⁻ ( n = 10) mice. Leukocytes were phenotyped by flow cytometry: CD11b + cells, monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺); inflammatory monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁺); and Ly6C⁻ monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁻). Shaded area indicates mean and SEM of total leukocyte frequency. p -values were calculated using Šídák’s multiple-comparisons test. C Serum cytokine levels in WT ( n = 6) and CD5L⁻ ( n = 6) mice. p -values were calculated using the Mann–Whitney test. D Serum RANKL and <t>cross-linked</t> <t>C-telopeptide</t> of <t>type</t> <t>I</t> collagen <t>(CTX-I)</t> levels on day 56 after immunization. p -values were obtained using an unpaired t -test with Welch’s correction. E Splenic gene expression in non-immunized WT ( n = 5) and CD5L⁻ ( n = 5) mice, measured by RT-qPCR and normalized to Actb (β-actin). p -values were calculated using a two-tailed unpaired t -test with Welch’s correction
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    Immune profile of WT and CD5L⁻ mice during CIA. A Serum CD5L levels measured in WT mice after immunization. p -values were obtained using the Kruskal–Wallis test with Dunn’s multiple comparisons. B Frequencies of blood leukocyte subsets in WT ( n = 10) and CD5L⁻ ( n = 10) mice. Leukocytes were phenotyped by flow cytometry: CD11b + cells, monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺); inflammatory monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁺); and Ly6C⁻ monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁻). Shaded area indicates mean and SEM of total leukocyte frequency. p -values were calculated using Šídák’s multiple-comparisons test. C Serum cytokine levels in WT ( n = 6) and CD5L⁻ ( n = 6) mice. p -values were calculated using the Mann–Whitney test. D Serum RANKL and cross-linked C-telopeptide of type I collagen (CTX-I) levels on day 56 after immunization. p -values were obtained using an unpaired t -test with Welch’s correction. E Splenic gene expression in non-immunized WT ( n = 5) and CD5L⁻ ( n = 5) mice, measured by RT-qPCR and normalized to Actb (β-actin). p -values were calculated using a two-tailed unpaired t -test with Welch’s correction

    Journal: Molecular Medicine

    Article Title: CD5L insufficiency exacerbates skeletal joint damage in rheumatoid arthritis

    doi: 10.1186/s10020-026-01456-x

    Figure Lengend Snippet: Immune profile of WT and CD5L⁻ mice during CIA. A Serum CD5L levels measured in WT mice after immunization. p -values were obtained using the Kruskal–Wallis test with Dunn’s multiple comparisons. B Frequencies of blood leukocyte subsets in WT ( n = 10) and CD5L⁻ ( n = 10) mice. Leukocytes were phenotyped by flow cytometry: CD11b + cells, monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺); inflammatory monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁺); and Ly6C⁻ monocytes (Siglec-F⁻Ly6G⁻F4/80⁺CD11b⁺Ly6C⁻). Shaded area indicates mean and SEM of total leukocyte frequency. p -values were calculated using Šídák’s multiple-comparisons test. C Serum cytokine levels in WT ( n = 6) and CD5L⁻ ( n = 6) mice. p -values were calculated using the Mann–Whitney test. D Serum RANKL and cross-linked C-telopeptide of type I collagen (CTX-I) levels on day 56 after immunization. p -values were obtained using an unpaired t -test with Welch’s correction. E Splenic gene expression in non-immunized WT ( n = 5) and CD5L⁻ ( n = 5) mice, measured by RT-qPCR and normalized to Actb (β-actin). p -values were calculated using a two-tailed unpaired t -test with Welch’s correction

    Article Snippet: C-telopeptide cross-link type I collagen (CTX-I) was measured by an ELISA (IDS Serum CrossLaps, Immunodiagnostic Systems, Boldon, UK) in undiluted samples; detection limit, 0.11 ng/ml.

    Techniques: Flow Cytometry, MANN-WHITNEY, Gene Expression, Quantitative RT-PCR, Two Tailed Test