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anti col3a1  (Proteintech)


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    Structured Review

    Proteintech anti col3a1
    Anti Col3a1, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 603 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/col3a1+antibody/Collagen+Type+III+(N-terminal)+Polyclonal+antibody/pm41915213-136-33-36
    Average 96 stars, based on 603 article reviews
    anti col3a1 - by Bioz Stars, 2026-09
    96/100 stars

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    other:

    Article Title: Roles of m 6 A modification in regulating PPER pathway in cadmium-induced pancreatic β cell death.
    Article Snippet: Cadmium can lead to the death of pancreatic β cells, thus affecting the synthesis and secretion of insulin.. However, the specific mechanisms underlying the cadmium-induced pancreatic β cell death have not been fully understood.. In this study, roles of m6A modification in regulating protein processing in endoplasmic reticulum (PPER) pathway in cadmium-induced pancreatic β cell death were explored.

    Article Title: Magnesium ions attenuate tendon graft fibrosis during its ligamentization after ACL reconstruction through modulation of fibroblast to myofibroblast trans-differentiation by promoting PGE2 secretion
    Article Snippet: Antibodies used in this study were listed as follows: α-SMA (Proteintech, China), COL1A1 (Proteintech, China), COL3A1 (Proteintech, China), TGF-β1 (Proteintech, China), PGE2 (Proteintech, China), CD68 (Proteintech, China), HRP-conjugated anti-rabbit (Servicebio, China) or anti-mouse (Servicebio, China) secondary antibodies.

    Article Title: Therapeutic Effects of Long-Term Administration of Tranilast in an Animal Model for the Treatment of Fibroids
    Article Snippet: After transferring the samples to a nitrocellulose membrane, the membrane was blocked with TBS-Tween + 5% milk and probed with the following primary antibodies: COL3A1 and FN1 (Proteintech Group, Inc., Chicago, IL, USA), CCND1 (Cell Signaling Technology, Danvers, MA, USA), and E2F1 (Santa Cruz Biotechnology, Dallas, TX, USA).

    Article Title: Therapeutic Effects of Long-Term Administration of Tranilast in an Animal Model for the Treatment of Fibroids.
    Article Snippet: After transferring the samples to a nitrocellulose membrane, the membrane was blocked with TBS-Tween + 5% milk and probed with the following primary antibodies: COL3A1 and FN1 (Proteintech Group, Inc., Chicago, IL, USA), CCND1 (Cell Signaling Technology, Danvers, MA, USA), and E2F1 Int.

    Article Title: LARP6 Regulates Keloid Fibroblast Proliferation, Invasion, and Ability to Synthesize Collagen.
    Article Snippet: The membranes were blocked with 5% dried skimmed milk in PBS for 1 hour and incubated with the primary antibodies against LARP6 (1:500 dilution, Thermo Fisher Scientific, Waltham, MA), COL1A1 (1:500 dilution, ProteinTech), COL1A2 (1:500 dilution, ProteinTech), COL3A1 (1:500 L Chen et al. Upregulated LARP6 Facilitates Keloid Growth and Invasion dilution, ProteinTech) or b-actin (1:1,000 dilution, ProteinTech) at 4 C overnight, followed by incubation with horseradish peroxidase‒conjugated secondary antibodies (1:1,000 dilution) for 1 hour at 37 C. The enhancement working solution was prepared by mixing the ECL reagent with the stable peroxidase solution in a ratio of 1:1 and adding it dropwise to the polyvinylidene difluoride membrane for color exposure.

    Blocking Assay:

    Article Title: Faecalibacterium prausnitzii-derived extracellular vesicles alleviate chronic colitis-related intestinal fibrosis by macrophage metabolic reprogramming.
    Article Snippet: .. After antigen retrieval and BSA blocking, the tissue sections were incubated at 4◦C overnight with Clo1a1 antibody (1:100; #72026, Cell Signaling Technology, USA), Col3a1 antibody (1:500; 22734–1-AP, Proteintech, Wuhan, China), Vimentin antibody (1:200; ab92547, abcam, UK) and TGF-β1 antibody (1:500; ab215715, abcam, UK), then rinsed with PBS for 30 min, and incubated again with secondary antibodies for 20 min at ambient temperature (Zhongshang Goldenbridge). ..

    Incubation:

    Article Title: Faecalibacterium prausnitzii-derived extracellular vesicles alleviate chronic colitis-related intestinal fibrosis by macrophage metabolic reprogramming.
    Article Snippet: .. After antigen retrieval and BSA blocking, the tissue sections were incubated at 4◦C overnight with Clo1a1 antibody (1:100; #72026, Cell Signaling Technology, USA), Col3a1 antibody (1:500; 22734–1-AP, Proteintech, Wuhan, China), Vimentin antibody (1:200; ab92547, abcam, UK) and TGF-β1 antibody (1:500; ab215715, abcam, UK), then rinsed with PBS for 30 min, and incubated again with secondary antibodies for 20 min at ambient temperature (Zhongshang Goldenbridge). ..

    Recombinant:

    Article Title: Identifying fibroblast-derived sFRP2 as a therapeutic target and engineering siRNA therapy for uterine scarring
    Article Snippet: 1,2-Dimyristoyl-rac-glycero-3-methoxypolyethylene glycol-2000 (DMG-PEG) was purchased from Suzhou Highfine Biotech Co., Ltd. RIPA lysis buffer and BCA protein assay kit were purchased from Wuhan Servicebio Technology Co. .. The companies and catalog numbers of different antibodies and recombinant proteins are as followed: sFRP2 antibody (Proteintech, 66328-1-lg), VEGFA antibody (Proteintech, 19003-1-AP), α-SMA antibody (Proteintech, 14395-1-AP), fibrinogen antibody (Proteintech, 20645-1-AP), Col1A1 antibody (Proteintech, 14695-1-AP), Col3A1 antibody (Proteintech, 22734-1-AP), vimentin antibody (Proteintech, 10366-1-AP), WNT5A antibody (Affinity, DF6856), Ki67 antibody (Proteintech, 27309-1-AP), cytokeratin 7 antibody (CK7, Proteintech, 15539-1-AP), Flag tag antibody (Proteintech, 66008-4-lg), HA tag antibody (ABclonal, AE105), FZD5 antibody (ABclonal, A12775), myeloperoxidase (MPO) polyclonal antibody (Proteintech, 22225-1-AP), F4/80 antibody (Servicebio, GB113373 ), CD3 antibody (Servicebio, GB150004 ), GAPDH antibody (Proteintech, 60004-1-lg), β-actin antibody (Proteintech, 66009-1-lg), FITC-conjugated affinipure goat anti-Rabbit IgG (Proteintech, SA00003-2), Cy3-conjugated affinipure goat anti-Mouse IgG (Proteintech, SA00009-1), recombinant human TGF-β protein (Proteintech, HZ1011), recombinant human sFRP2 protein (rhsFRP2, MedChemExpress, HY- P77835 ), recombinant human WNT5A protein (R&D, 645-WN). .. DMEM/F12K and DMEM were obtained from Gibco (U.S.A.).

    FLAG-tag:

    Article Title: Identifying fibroblast-derived sFRP2 as a therapeutic target and engineering siRNA therapy for uterine scarring
    Article Snippet: 1,2-Dimyristoyl-rac-glycero-3-methoxypolyethylene glycol-2000 (DMG-PEG) was purchased from Suzhou Highfine Biotech Co., Ltd. RIPA lysis buffer and BCA protein assay kit were purchased from Wuhan Servicebio Technology Co. .. The companies and catalog numbers of different antibodies and recombinant proteins are as followed: sFRP2 antibody (Proteintech, 66328-1-lg), VEGFA antibody (Proteintech, 19003-1-AP), α-SMA antibody (Proteintech, 14395-1-AP), fibrinogen antibody (Proteintech, 20645-1-AP), Col1A1 antibody (Proteintech, 14695-1-AP), Col3A1 antibody (Proteintech, 22734-1-AP), vimentin antibody (Proteintech, 10366-1-AP), WNT5A antibody (Affinity, DF6856), Ki67 antibody (Proteintech, 27309-1-AP), cytokeratin 7 antibody (CK7, Proteintech, 15539-1-AP), Flag tag antibody (Proteintech, 66008-4-lg), HA tag antibody (ABclonal, AE105), FZD5 antibody (ABclonal, A12775), myeloperoxidase (MPO) polyclonal antibody (Proteintech, 22225-1-AP), F4/80 antibody (Servicebio, GB113373 ), CD3 antibody (Servicebio, GB150004 ), GAPDH antibody (Proteintech, 60004-1-lg), β-actin antibody (Proteintech, 66009-1-lg), FITC-conjugated affinipure goat anti-Rabbit IgG (Proteintech, SA00003-2), Cy3-conjugated affinipure goat anti-Mouse IgG (Proteintech, SA00009-1), recombinant human TGF-β protein (Proteintech, HZ1011), recombinant human sFRP2 protein (rhsFRP2, MedChemExpress, HY- P77835 ), recombinant human WNT5A protein (R&D, 645-WN). .. DMEM/F12K and DMEM were obtained from Gibco (U.S.A.).



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    Image Search Results


    NAD metabolism is disrupted in tendinopathic tendons in vivo . a . A schematic diagram of the harvested region of human Achilles tendons. (The mid-portion of Achilles tendon) and the gross image of healthy and AT tendons. b. NAD + /NADH ratio and quantification of NAD metabolism (including, NAD + , NADH, total NAD pool) in human Achilles tendons. c. Quantification of ATP production. d. GSEA revealing top NAD metabolism-related GO terms enriched in human Achilles tendons. e. GSEA revealing top degeneration-related GO terms enriched in human Achilles tendon. f. Images of H&E staining, AB (Alcian blue) staining and Masson staining of human normal tendons and tendinopathic tendons. Bonar scores. g. Immunohistochemical staining of COL1 and COL3. h. Immunohistochemical staining of PARP and NOX4. i. Quantitative analysis of COL1, COL3, PARP, NOX4, and ratio of COL3/COL1. j. Immunohistochemical staining and quantification of TUNEL. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: NAD metabolism is disrupted in tendinopathic tendons in vivo . a . A schematic diagram of the harvested region of human Achilles tendons. (The mid-portion of Achilles tendon) and the gross image of healthy and AT tendons. b. NAD + /NADH ratio and quantification of NAD metabolism (including, NAD + , NADH, total NAD pool) in human Achilles tendons. c. Quantification of ATP production. d. GSEA revealing top NAD metabolism-related GO terms enriched in human Achilles tendons. e. GSEA revealing top degeneration-related GO terms enriched in human Achilles tendon. f. Images of H&E staining, AB (Alcian blue) staining and Masson staining of human normal tendons and tendinopathic tendons. Bonar scores. g. Immunohistochemical staining of COL1 and COL3. h. Immunohistochemical staining of PARP and NOX4. i. Quantitative analysis of COL1, COL3, PARP, NOX4, and ratio of COL3/COL1. j. Immunohistochemical staining and quantification of TUNEL. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: In Vivo, Staining, Immunohistochemical staining, TUNEL Assay

    MB corrects NAD dysmetabolism and matrix degeneration in the rat tendinopathy model. a . A schematic illustration of the rat tendinopathy model. b. Gross image of the Rat AT model. c. Gait analysis results for the different groups. The blue dotted line represents stride length; the red dotted line represents step length. Blue print: forepaw; red print: hind paw. d. Quantification of stride length, step length, and the length of the front/rear paw prints. e. Hot plate test. f. Paw contraction thresholds were assessed utilizing von Frey fibers to gauge mechanical sensitivity (n = 6). g. Quantification of ATP in the rat AT model. h. NAD + /NADH ratio i. Quantification of NAD metabolism (including, NAD + , NADH, total NAD pool). j. H&E staining, AB staining and Masson staining. Bonar scores of rats AT model. k. Immunohistochemical staining of Col1 and Col3. l. Immunohistochemical staining of Parp and Nox4. m. Quantitative analysis of Col1, Col3, Parp, Nox4. n. TUNEL staining and quantitative analysis of apoptotic cells. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: MB corrects NAD dysmetabolism and matrix degeneration in the rat tendinopathy model. a . A schematic illustration of the rat tendinopathy model. b. Gross image of the Rat AT model. c. Gait analysis results for the different groups. The blue dotted line represents stride length; the red dotted line represents step length. Blue print: forepaw; red print: hind paw. d. Quantification of stride length, step length, and the length of the front/rear paw prints. e. Hot plate test. f. Paw contraction thresholds were assessed utilizing von Frey fibers to gauge mechanical sensitivity (n = 6). g. Quantification of ATP in the rat AT model. h. NAD + /NADH ratio i. Quantification of NAD metabolism (including, NAD + , NADH, total NAD pool). j. H&E staining, AB staining and Masson staining. Bonar scores of rats AT model. k. Immunohistochemical staining of Col1 and Col3. l. Immunohistochemical staining of Parp and Nox4. m. Quantitative analysis of Col1, Col3, Parp, Nox4. n. TUNEL staining and quantitative analysis of apoptotic cells. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: Hot Plate Test, Staining, Immunohistochemical staining, TUNEL Assay

    MB reduces TBHP-induced NAD metabolism disorder in vitro and in vivo. a . The cell viability. b. Quantitation of NAD metabolism (including NAD + /NADH ratio, NAD + , NADH, total NAD pool) in rat tenocytes. c. Quantitation of ATP in rat tenocytes. d. Representative Western blot results for Col3, Col1, MMP3, and MMP13 in rat tenocytes. e. Ratio of Col3/Col1 by d. f. Representative Western blot results for Parp, c-Parp, Nox4, Bcl2, and Bax. g, h. Immunofluorescence and quantification analysis of Col1, Col3, Parp, and Nox4 expression in rat tenocytes. The ratio of Col1/Col3. DAPI, 4′,6-diamidino-2-phenylindole. i. Fluorescence images of the DCFH-DA probe for hydrogen peroxide in rat tenocytes. j. JC-1 staining in rat tenocytes. k. Quantitative analysis of ROS. l. Quantitative analysis of JC-1. m. Annexin V and activated caspase-3 staining and quantitative analysis of apoptotic cells in rat tenocytes. The results are presented as medians with 95% CIs. n = 3, 5, ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: MB reduces TBHP-induced NAD metabolism disorder in vitro and in vivo. a . The cell viability. b. Quantitation of NAD metabolism (including NAD + /NADH ratio, NAD + , NADH, total NAD pool) in rat tenocytes. c. Quantitation of ATP in rat tenocytes. d. Representative Western blot results for Col3, Col1, MMP3, and MMP13 in rat tenocytes. e. Ratio of Col3/Col1 by d. f. Representative Western blot results for Parp, c-Parp, Nox4, Bcl2, and Bax. g, h. Immunofluorescence and quantification analysis of Col1, Col3, Parp, and Nox4 expression in rat tenocytes. The ratio of Col1/Col3. DAPI, 4′,6-diamidino-2-phenylindole. i. Fluorescence images of the DCFH-DA probe for hydrogen peroxide in rat tenocytes. j. JC-1 staining in rat tenocytes. k. Quantitative analysis of ROS. l. Quantitative analysis of JC-1. m. Annexin V and activated caspase-3 staining and quantitative analysis of apoptotic cells in rat tenocytes. The results are presented as medians with 95% CIs. n = 3, 5, ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: In Vitro, In Vivo, Quantitation Assay, Western Blot, Immunofluorescence, Expressing, Fluorescence, Staining

    MB alleviates TBHP-induced tendinopathy in human Achilles tendon explant. a . A schematic illustration of the human extra explant. b. Quantification of NAD metabolism in human extra explants under TBHP treatment combined with or without MB. (n = 3) c. H&E staining, AB staining, and Masson staining of human tendon explants. The Bonar scores. d. Quantification of ATP in human tendon explants. e. NFR. f. Immunohistochemical staining of COL1 and COL3. g. Immunohistochemical staining of PARP and NOX4. h. Immunohistochemical staining of AIF and NDUFB8. i. Quantification of the immunohistochemical staining data. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: MB alleviates TBHP-induced tendinopathy in human Achilles tendon explant. a . A schematic illustration of the human extra explant. b. Quantification of NAD metabolism in human extra explants under TBHP treatment combined with or without MB. (n = 3) c. H&E staining, AB staining, and Masson staining of human tendon explants. The Bonar scores. d. Quantification of ATP in human tendon explants. e. NFR. f. Immunohistochemical staining of COL1 and COL3. g. Immunohistochemical staining of PARP and NOX4. h. Immunohistochemical staining of AIF and NDUFB8. i. Quantification of the immunohistochemical staining data. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 5; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: Staining, Immunohistochemical staining

    MB alleviates oxidative stress in a MC1-dependent manner in rat tenocytes. a. Quantification of ATP in rat tenocytes after TBHP treatment combined with/without MB or rotenone (Rot, a complex I inhibitor). b. NFR. c. Quantification of NAD metabolism. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Parp, Nox4, Aif expression by immunofluorescence microscopy (n = 3). f. Col3, Col1, Ndufb8 expression by immunofluorescence microscopy. g. Quantification of the immunofluorescence data from e and f . h. JC-1 staining. i. Quantitative analysis of JC-1. j, k. Fluorescence images and quantitative analysis of ROS. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: MB alleviates oxidative stress in a MC1-dependent manner in rat tenocytes. a. Quantification of ATP in rat tenocytes after TBHP treatment combined with/without MB or rotenone (Rot, a complex I inhibitor). b. NFR. c. Quantification of NAD metabolism. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Parp, Nox4, Aif expression by immunofluorescence microscopy (n = 3). f. Col3, Col1, Ndufb8 expression by immunofluorescence microscopy. g. Quantification of the immunofluorescence data from e and f . h. JC-1 staining. i. Quantitative analysis of JC-1. j, k. Fluorescence images and quantitative analysis of ROS. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: Western Blot, Expressing, Immunofluorescence, Microscopy, Staining, Fluorescence

    MB increases the expression of Aif under Aif knockdown in tenocytes. a. The NAD metabolism after Aif was knocked down in rat tenocytes. b. Quantification of ATP after Aif knockdown. c. NFR. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Quantification of the Western blot data from d. f. Quantification of the immunofluorescence staining data . g. Col3, Col1, Parp, Nox4, Ndufb8, and Aif expression by immunofluorescence microscopy; h. Fluorescence images of ROS. i. JC-1 staining. j. Quantification of DCFH-DA staining data. k. Quantification of JC-1 staining data. l. Schematic illustration of the mechanism of MB in tendinopathy. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Journal: Journal of Orthopaedic Translation

    Article Title: Methylene blue restores NAD + /NADH homeostasis to attenuate Achilles tendinopathy via activating AIF/Mitochondrial respiratory chain complex I

    doi: 10.1016/j.jot.2026.101085

    Figure Lengend Snippet: MB increases the expression of Aif under Aif knockdown in tenocytes. a. The NAD metabolism after Aif was knocked down in rat tenocytes. b. Quantification of ATP after Aif knockdown. c. NFR. d. Representative Western blot results for Parp, c-Parp, Nox4, Aif, Col3, Col1, and Ndufb8. e. Quantification of the Western blot data from d. f. Quantification of the immunofluorescence staining data . g. Col3, Col1, Parp, Nox4, Ndufb8, and Aif expression by immunofluorescence microscopy; h. Fluorescence images of ROS. i. JC-1 staining. j. Quantification of DCFH-DA staining data. k. Quantification of JC-1 staining data. l. Schematic illustration of the mechanism of MB in tendinopathy. Scale bar: 50 μm. The results are presented as medians with 95% CIs. n = 3; ∗, P < 0.05; ∗∗, P < 0.01; ∗∗∗, P < 0.001.

    Article Snippet: Then, for antigen retrieval, the sections were incubated with 0.4% pepsin (Sigma–Aldrich) in 1 mM hydrochloric acid at 37 °C for 1 h. After blocking with 5% bovine serum albumin for 30 min at 37 °C, the sections were incubated with primary antibody against Col1(1:1000, #ab138492, Abcam, UK), Col3(1:1000, #A00788-3, Boster, China), Nox4 (1:2000, #14347-1-AP, Proteintech, China), Parp (1:1000, #13371-1-AP, Proteintech, China), Aif (1:1000, #67791-1-Ig, Proteintech, China), Ndufb8 (1:1000, #67690-1-Ig, Proteintech, China), and Gapdh (1:2000, #2118, Cell Signaling Technology, USA) overnight at 4 °C and finally with an HRP-conjugated secondary antibody (#BL003A or #BL001A, Biosharp, China).

    Techniques: Expressing, Knockdown, Western Blot, Immunofluorescence, Staining, Microscopy, Fluorescence