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mmp13  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology mmp13
    Mmp13, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 414 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mmp+13/MMP-13+Antibody/pm41935436-52-9-20
    Average 95 stars, based on 414 article reviews
    mmp13 - by Bioz Stars, 2026-09
    95/100 stars

    Images

    Related Articles

    other:

    Article Title: p-Synephrine Loaded by Injectable Gelma Hydrogel Ameliorates Cartilage Degeneration in Osteoarthritis by Inhibiting the MAPK and NF-κB Signaling Pathways.
    Article Snippet: The antibodies against MMP-1, MMP-3, MMP-13, p-NF-κB p65, NF-κB p65, p-IκBα, IκBα, p-p38, and p38 were procured from the Santa Cruz Biotechnology Company (Santa Cruz, CA, U.S.A.).

    Blocking Assay:

    Article Title: Piezo1-driven mechanotransduction as a key regulator of cartilage degradation in early osteoarthritis
    Article Snippet: Proteins were separated using SDS-PAGE and transferred to membranes (1704156 and 1620176 from Bio-Rad). .. After blocking (37565 from Invitrogen), membranes were stained with primary antibodies against tubulin, Piezo1, MMP-13, ADAMTs5, Aggrecan, and Collagen II, all purchased from Santa Cruz Biotechnology. .. Membranes were then incubated overnight with horseradish peroxidase-conjugated secondary antibodies (31460 and 31430 from Invitrogen) and visualized by chemiluminescence.

    Article Title: Piezo1-driven mechanotransduction as a key regulator of cartilage degradation in early osteoarthritis.
    Article Snippet: Proteins were separated using SDS‒PAGE and transferred to membranes (1704156 and 1620176 from Bio-Rad). .. After blocking (37565 from Invitrogen), the membranes were stained with primary antibodies against tubulin, Piezo1, MMP-13, ADAMTs5, Aggrecan and Collagen II purchased from Santa Cruz Biotechnology. .. Then, the membranes were incubated with horseradish peroxidase-conjugated secondary antibodies (31460 and 31430 from Invitrogen) overnight and visualized by chemiluminescence.

    Staining:

    Article Title: Piezo1-driven mechanotransduction as a key regulator of cartilage degradation in early osteoarthritis
    Article Snippet: Proteins were separated using SDS-PAGE and transferred to membranes (1704156 and 1620176 from Bio-Rad). .. After blocking (37565 from Invitrogen), membranes were stained with primary antibodies against tubulin, Piezo1, MMP-13, ADAMTs5, Aggrecan, and Collagen II, all purchased from Santa Cruz Biotechnology. .. Membranes were then incubated overnight with horseradish peroxidase-conjugated secondary antibodies (31460 and 31430 from Invitrogen) and visualized by chemiluminescence.

    Article Title: Piezo1-driven mechanotransduction as a key regulator of cartilage degradation in early osteoarthritis.
    Article Snippet: Proteins were separated using SDS‒PAGE and transferred to membranes (1704156 and 1620176 from Bio-Rad). .. After blocking (37565 from Invitrogen), the membranes were stained with primary antibodies against tubulin, Piezo1, MMP-13, ADAMTs5, Aggrecan and Collagen II purchased from Santa Cruz Biotechnology. .. Then, the membranes were incubated with horseradish peroxidase-conjugated secondary antibodies (31460 and 31430 from Invitrogen) overnight and visualized by chemiluminescence.

    Saline:

    Article Title: Biomechanical and biological features of hyaluronic acid in combination with chondroitin and platelet rich plasma for regenerative medicine applications
    Article Snippet: A total of 15 μg of protein was electrophoretically separated on a 10% SDS-PAGE polyacrylamide gel and transferred onto nitrocellulose membrane (GE, Amersham, United Kingdom). .. This latter was washed with tris-buffered saline containing 0.05% v/v Tween-20 (Bio-Rad Laboratories, Milan, Italy) (TTBS) and blocked with 5% w/v non-fat milk (Bio-Rad Laboratories, Milan, Italy) in TTBS for 30 min and successively incubated overnight at 4 °C with primary antibodies (all diluted 1:500 v/v) against COMP-2 (Santa Cruz Biotechnology, Dallas, TX, United States), NF-κB (Santa Cruz Biotechnology, Dallas, TX, United States), MMP-13 (Santa Cruz Biotechnology, Dallas, TX, United States), Collagen 2A1 (COL2A1) (Elabscience, Houston, TX, United States), Aggrecan (ACAN) (Santa Cruz Biotechnology, Dallas, TX, United States) and HAS-2 (Santa Cruz Biotechnology, Dallas, TX, United States). .. The following day, the membrane was gently washed with TTBS and incubated with specific secondary horseradish peroxidase-conjugated antibodies (Santa Cruz Biotechnology, Dallas, TX, United States) diluted 1:1,000 v/v for 2 h at room temperature.

    Incubation:

    Article Title: Biomechanical and biological features of hyaluronic acid in combination with chondroitin and platelet rich plasma for regenerative medicine applications
    Article Snippet: A total of 15 μg of protein was electrophoretically separated on a 10% SDS-PAGE polyacrylamide gel and transferred onto nitrocellulose membrane (GE, Amersham, United Kingdom). .. This latter was washed with tris-buffered saline containing 0.05% v/v Tween-20 (Bio-Rad Laboratories, Milan, Italy) (TTBS) and blocked with 5% w/v non-fat milk (Bio-Rad Laboratories, Milan, Italy) in TTBS for 30 min and successively incubated overnight at 4 °C with primary antibodies (all diluted 1:500 v/v) against COMP-2 (Santa Cruz Biotechnology, Dallas, TX, United States), NF-κB (Santa Cruz Biotechnology, Dallas, TX, United States), MMP-13 (Santa Cruz Biotechnology, Dallas, TX, United States), Collagen 2A1 (COL2A1) (Elabscience, Houston, TX, United States), Aggrecan (ACAN) (Santa Cruz Biotechnology, Dallas, TX, United States) and HAS-2 (Santa Cruz Biotechnology, Dallas, TX, United States). .. The following day, the membrane was gently washed with TTBS and incubated with specific secondary horseradish peroxidase-conjugated antibodies (Santa Cruz Biotechnology, Dallas, TX, United States) diluted 1:1,000 v/v for 2 h at room temperature.



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    Efficacy of mechanically sensitized OBNC microspheres in the treatment of osteoarthritis. A) Diagram of OBNC microspheres self-adaptive filling of a cartilage injury site to promote cartilage repair and regeneration. B) Representative images of H&E staining. C) OARSI scores of articular cartilage in each group. D) Representative images of safranin O-fast green staining. E) Relative glycosaminoglycan (GAG) content in each group. F) Representative sections showing TUNEL staining for apoptotic cells. G) Quantification of TUNEL-positive cells. H) Representative sections showing Collagen II staining for chondrocytes. I) Relative collagen II expression in each group. J) Representative sections <t>showing</t> <t>MMP-13</t> staining of chondrocytes. K) Relative MMP-13 expression in each group. (ns: non-significant, ∗ P < 0.05, ∗∗ P < 0.01).
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    Efficacy of mechanically sensitized OBNC microspheres in the treatment of osteoarthritis. A) Diagram of OBNC microspheres self-adaptive filling of a cartilage injury site to promote cartilage repair and regeneration. B) Representative images of H&E staining. C) OARSI scores of articular cartilage in each group. D) Representative images of safranin O-fast green staining. E) Relative glycosaminoglycan (GAG) content in each group. F) Representative sections showing TUNEL staining for apoptotic cells. G) Quantification of TUNEL-positive cells. H) Representative sections showing Collagen II staining for chondrocytes. I) Relative collagen II expression in each group. J) Representative sections <t>showing</t> <t>MMP-13</t> staining of chondrocytes. K) Relative MMP-13 expression in each group. (ns: non-significant, ∗ P < 0.05, ∗∗ P < 0.01).
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    Efficacy of mechanically sensitized OBNC microspheres in the treatment of osteoarthritis. A) Diagram of OBNC microspheres self-adaptive filling of a cartilage injury site to promote cartilage repair and regeneration. B) Representative images of H&E staining. C) OARSI scores of articular cartilage in each group. D) Representative images of safranin O-fast green staining. E) Relative glycosaminoglycan (GAG) content in each group. F) Representative sections showing TUNEL staining for apoptotic cells. G) Quantification of TUNEL-positive cells. H) Representative sections showing Collagen II staining for chondrocytes. I) Relative collagen II expression in each group. J) Representative sections <t>showing</t> <t>MMP-13</t> staining of chondrocytes. K) Relative MMP-13 expression in each group. (ns: non-significant, ∗ P < 0.05, ∗∗ P < 0.01).
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    Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 <t>and</t> <t>MMP-13</t> in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.
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    Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 <t>and</t> <t>MMP-13</t> in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.
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    Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 <t>and</t> <t>MMP-13</t> in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.
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    Santa Cruz Biotechnology ◦ c
    Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 <t>and</t> <t>MMP-13</t> in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.
    ◦ C, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Efficacy of mechanically sensitized OBNC microspheres in the treatment of osteoarthritis. A) Diagram of OBNC microspheres self-adaptive filling of a cartilage injury site to promote cartilage repair and regeneration. B) Representative images of H&E staining. C) OARSI scores of articular cartilage in each group. D) Representative images of safranin O-fast green staining. E) Relative glycosaminoglycan (GAG) content in each group. F) Representative sections showing TUNEL staining for apoptotic cells. G) Quantification of TUNEL-positive cells. H) Representative sections showing Collagen II staining for chondrocytes. I) Relative collagen II expression in each group. J) Representative sections showing MMP-13 staining of chondrocytes. K) Relative MMP-13 expression in each group. (ns: non-significant, ∗ P < 0.05, ∗∗ P < 0.01).

    Journal: Bioactive Materials

    Article Title: Mechanically sensitized hydrogel microspheres trigger membrane receptor switch for cartilage repair

    doi: 10.1016/j.bioactmat.2026.03.017

    Figure Lengend Snippet: Efficacy of mechanically sensitized OBNC microspheres in the treatment of osteoarthritis. A) Diagram of OBNC microspheres self-adaptive filling of a cartilage injury site to promote cartilage repair and regeneration. B) Representative images of H&E staining. C) OARSI scores of articular cartilage in each group. D) Representative images of safranin O-fast green staining. E) Relative glycosaminoglycan (GAG) content in each group. F) Representative sections showing TUNEL staining for apoptotic cells. G) Quantification of TUNEL-positive cells. H) Representative sections showing Collagen II staining for chondrocytes. I) Relative collagen II expression in each group. J) Representative sections showing MMP-13 staining of chondrocytes. K) Relative MMP-13 expression in each group. (ns: non-significant, ∗ P < 0.05, ∗∗ P < 0.01).

    Article Snippet: Antigen retrieval was performed by microwaving in citrate buffer for 10 min. Endogenous peroxidase activity was blocked by incubating the sections with 3% hydrogen peroxide for 10 min, and non-specific binding was blocked with 3% BSA for 1 h. The sections were incubated overnight at 4 °C with primary antibodies to Collagen II and MMP-13 (ServiceBio, China), washed, and incubated for 1 h with HRP-labeled secondary antibodies (ServiceBio, China).

    Techniques: Staining, TUNEL Assay, Expressing

    Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 and MMP-13 in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.

    Journal: Non-coding RNA Research

    Article Title: Hsa_circ_0101645 contributes to excessive autophagy and apoptosis in intervertebral disc degeneration by acting as a miR-1304-5p sponge modulating BNIP3 expression

    doi: 10.1016/j.ncrna.2025.11.007

    Figure Lengend Snippet: Hsa_circ_0101645 accelerating the IVDD process in vivo . A: Diagram of the animal procedure for this study. B: Grouping information for this section. C: Representative X-rays of each group of rats. Statistical graph demonstrating the disc height index (DHI) changes for L4/5 in each group of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). D: HE staining exhibiting pathological changes of CEP, NP, and AP in IVD in each group of rats (N = 6). Scale bar: 500 μm. E: EdU staining was used to detect cell proliferation in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. F: TUNEL (white light) staining exhibiting TUNEL-positive cells in IVD tissues of rats (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 50 μm. G: The effect of hsa_circ_0101645 on the protein levels of Collagen Ⅱ, Aggrecan, MMP-3 and MMP-13 in IVD was observed by IHC staining (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). Scale bar: 100 μm. H-I: The expression of hsa_circ_0101645 (H) and miR-1304-5p (I) in each group of IVD tissues (N = 6) (One-way ANOVA test with Tukey's multiple comparisons test). J-K: Changes in expression of apoptosis ( J; Caspase 3, Bcl-2 and Bax) and autophagy markers ( K; LC3B, Beclin and P62) in IVD tissues (N = 3) (One-way ANOVA test with Tukey's multiple comparisons test or Kruskal-Wallis test with Dunn's multiple comparisons test). ∗ indicates P < 0.05.

    Article Snippet: Sections were then incubated with primary antibodies against Collagen II (28459-1-AP; 1:200; Proteintech, USA), Aggrecan (13880-1-AP; 1:100; Proteintech), MMP-3 (17873-1-AP; 1:200; Proteintech), and MMP-13 (18165-1-AP; 1:100; Proteintech), followed by the corresponding secondary antibodies.

    Techniques: In Vivo, Staining, TUNEL Assay, Immunohistochemistry, Expressing