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rabbit anti col ii polyclonal antibody  (Bioss)


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    Structured Review

    Bioss rabbit anti col ii polyclonal antibody
    Rabbit Anti Col Ii Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti col ii polyclonal antibody/product/Bioss
    Average 90 stars, based on 5 article reviews
    rabbit anti col ii polyclonal antibody - by Bioz Stars, 2026-03
    90/100 stars

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    Preparation and characterization of CACM and SIM@CACM microgel: a) schematic illustration on CACM extraction process from natural articular cartilage (NAC); b) GAGs, DNA and <t>Col</t> <t>II</t> retention of NAC and CACM; c) histological staining including H&E staining, Alcian blue staining and safranin O staining; d) optical images of CACM gelation; e) optical images of SIM@CACM microgels in oil phase and water phase; f) size distribution of SIM@CACM microgels in water phase. ∗∗∗P < 0.001, ∗∗P < 0.01, n = 4.
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    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    iDNA Biotechnology rabbit anti-sheep col ii, sox9 col polyclonal antibodies
    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    Proteintech rabbit anti col ii
    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    Cell Signaling Technology Inc rabbit polyclonal anti col ii
    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent <t>Col-II</t> staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.
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    Image Search Results


    Preparation and characterization of CACM and SIM@CACM microgel: a) schematic illustration on CACM extraction process from natural articular cartilage (NAC); b) GAGs, DNA and Col II retention of NAC and CACM; c) histological staining including H&E staining, Alcian blue staining and safranin O staining; d) optical images of CACM gelation; e) optical images of SIM@CACM microgels in oil phase and water phase; f) size distribution of SIM@CACM microgels in water phase. ∗∗∗P < 0.001, ∗∗P < 0.01, n = 4.

    Journal: Bioactive Materials

    Article Title: Injectable acellular matrix microgel assembly with stem cell recruitment and chondrogenic differentiation functions promotes microfracture-based articular cartilage regeneration

    doi: 10.1016/j.bioactmat.2024.10.013

    Figure Lengend Snippet: Preparation and characterization of CACM and SIM@CACM microgel: a) schematic illustration on CACM extraction process from natural articular cartilage (NAC); b) GAGs, DNA and Col II retention of NAC and CACM; c) histological staining including H&E staining, Alcian blue staining and safranin O staining; d) optical images of CACM gelation; e) optical images of SIM@CACM microgels in oil phase and water phase; f) size distribution of SIM@CACM microgels in water phase. ∗∗∗P < 0.001, ∗∗P < 0.01, n = 4.

    Article Snippet: Specifically, cells were fixed, blocked with 2 % BSA/PBS, and labelled in turn with rabbit polyclonal anti-Col II antibody (Servicebio, China) overnight at 4 °C, FITC-conjugated phospholipid-like protein (Servicebio, China) and DAPI (Servicebio, China).

    Techniques: Extraction, Staining

    In vitro chondrogenic differentiation of BMSCs cultured on SIM@CACM microgel assembly: a) fluorescence images of DAPI, F-actin and Col II; b) fluorescence intensities of DAPI, F-actin and Col II; c) immunohistochemical (IHC) staining of Col II; d) mRNA expression. ∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05, n = 4.

    Journal: Bioactive Materials

    Article Title: Injectable acellular matrix microgel assembly with stem cell recruitment and chondrogenic differentiation functions promotes microfracture-based articular cartilage regeneration

    doi: 10.1016/j.bioactmat.2024.10.013

    Figure Lengend Snippet: In vitro chondrogenic differentiation of BMSCs cultured on SIM@CACM microgel assembly: a) fluorescence images of DAPI, F-actin and Col II; b) fluorescence intensities of DAPI, F-actin and Col II; c) immunohistochemical (IHC) staining of Col II; d) mRNA expression. ∗∗∗P < 0.001, ∗∗P < 0.01, ∗P < 0.05, n = 4.

    Article Snippet: Specifically, cells were fixed, blocked with 2 % BSA/PBS, and labelled in turn with rabbit polyclonal anti-Col II antibody (Servicebio, China) overnight at 4 °C, FITC-conjugated phospholipid-like protein (Servicebio, China) and DAPI (Servicebio, China).

    Techniques: In Vitro, Cell Culture, Fluorescence, Immunohistochemical staining, Immunohistochemistry, Expressing

    a) Safranin O-fast green staining and b) immunohistochemical staining of Col II after implanting normal saline (blank), SIM@CACM microgels, CACM microgel assembly and SIM@CACM microgel assembly respectively for 4 and 8 weeks; c) evaluation of cartilage repair performance via ICRS scoring system; d) evaluation of cartilage repair performance via O'Driscoll scoring system; NC stands for newborn cartilage, and OC stands for original cartilage.

    Journal: Bioactive Materials

    Article Title: Injectable acellular matrix microgel assembly with stem cell recruitment and chondrogenic differentiation functions promotes microfracture-based articular cartilage regeneration

    doi: 10.1016/j.bioactmat.2024.10.013

    Figure Lengend Snippet: a) Safranin O-fast green staining and b) immunohistochemical staining of Col II after implanting normal saline (blank), SIM@CACM microgels, CACM microgel assembly and SIM@CACM microgel assembly respectively for 4 and 8 weeks; c) evaluation of cartilage repair performance via ICRS scoring system; d) evaluation of cartilage repair performance via O'Driscoll scoring system; NC stands for newborn cartilage, and OC stands for original cartilage.

    Article Snippet: Specifically, cells were fixed, blocked with 2 % BSA/PBS, and labelled in turn with rabbit polyclonal anti-Col II antibody (Servicebio, China) overnight at 4 °C, FITC-conjugated phospholipid-like protein (Servicebio, China) and DAPI (Servicebio, China).

    Techniques: Staining, Immunohistochemical staining, Saline

    Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent Col-II staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.

    Journal: Bioactive Materials

    Article Title: L-arginine loading porous PEEK promotes percutaneous tissue repair through macrophage orchestration

    doi: 10.1016/j.bioactmat.2024.05.025

    Figure Lengend Snippet: Histological analysis of the tissue around samples. (a) Representative HE staining images of tissue around the samples post implantation for 1 month (the green arrows mark the neutrophil in tissue around samples and the blue arrows mark the newly formed vessels in the tissue around samples). (b) Quantitative bone area calculated by HE (n = 3); (c) Represent Col-II staining images of bone tissue around the samples post implantation for 1 month; (d) Quantitative positive area of Col-II (n = 4). Data are presented by mean with SD. Statistical significance was calculated by one-way ANOVA analysis. **p < 0.01, ***p < 0.001, ****p < 0.0001, compared with SPLA10 in b and d.

    Article Snippet: For immunohistochemistry staining, rabbit polyclonal anti-Col-III antibody (Servicebio, GB111629, 1: 500) and rabbit polyclonal anti-Col-II antibody (Servicebio, GB11021, 1: 200), and secondary antibody, HRP-labeled goat anti-rabbit IgG (Servicebio, GB23303, 1: 200), were used to stain Col-III and Col-II, respectively.

    Techniques: Staining