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collagen iii  (Proteintech)


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    Structured Review

    Proteintech collagen iii
    Collagen Iii, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 608 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/22734+1+ap/Collagen+Type+III+(N-terminal)+Polyclonal+antibody/pm40913688-74-22-26
    Average 96 stars, based on 608 article reviews
    collagen iii - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    other:

    Article Title: Fibroblast growth factor-inducible 14 accelerates pulmonary fibrosis by inducing fibroblast senescence in mice
    Article Snippet: Anti-Collagen III polyclonal antibody , Proteintech , 22734-1-AP , 1: 2000.

    Article Title: Decoding HuH-7: a comprehensive genetic and molecular portrait of a widely used hepatocellular carcinoma model
    Article Snippet: Collagen III , 22734-1-AP , AB_2879158 , Proteintech , 1:1,000 , r pAb.

    Article Title: Betulinic acid as a novel AT1R inhibitor: attenuation of liver fibrosis via modulation of endothelial–mesenchymal transition in chronic hepatic injury
    Article Snippet: Anti-Collagen III , 40,068,596 , Proteintech , 22734-1-AP , Polyclonal.

    Incubation:

    Article Title: Ustekinumab enhances intestinal stenosis resolution by modulating fibrotic pathways in crohn’s disease: a retrospective single-center study with translational analysis
    Article Snippet: .. The membranes were incubated overnight at 4°C with the following antibodies: mouse anti-collagen 1a1 (COL1A1) (1:1000; sc-293182; Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-collagen 3a1 (COL3A1) (1:1000; 22734-1-AP; Proteintech, Rosemont, IL, USA), and rabbit anti-GAPDH (1:10,000; G9545; Sigma-Aldrich, St. Louis, MO, USA). .. Proteins were detected using appropriate secondary antibodies conjugated to horseradish peroxidase and an enhanced chemiluminescence system (Amersham ECL Prime Western Blotting Detection Reagent; GE Healthcare Life Sciences, Buckinghamshire, UK).

    Article Title: Ustekinumab enhances intestinal stenosis resolution by modulating fibrotic pathways in crohn's disease: a retrospective single-center study with translational analysis.
    Article Snippet: .. The membranes were incubated overnight at 4°C with the following antibodies: mouse anti-collagen 1a1 (COL1A1) (1:1000; sc-293182; Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-collagen 3a1 (COL3A1) (1:1000; 22734-1-AP; Proteintech, Rosemont, IL, USA), and rabbit anti-GAPDH (1:10,000; G9545; Sigma-Aldrich, St. Louis, MO, USA). .. Proteins were detected using appropriate secondary antibodies conjugated to horseradish peroxidase and an enhanced chemiluminescence system (Amersham ECL Prime Western Blotting Detection Reagent; GE Healthcare Life Sciences, Buckinghamshire, UK).

    Staining:

    Article Title: A clinically translatable pathomics-based predictive model for preoperative prognostic assessment in patients with endometrial cancer.
    Article Snippet: .. The primary antibody against p-MEK and p-ERK were used at a dilution of 1:1500 (Proteintech, 22734-1-AP), and staining was carried out following the UltraVision Quanto Detection System protocol (Thermo Fisher Scientific). ..

    Article Title: A clinically translatable pathomics-based predictive model for preoperative prognostic assessment in patients with endometrial cancer
    Article Snippet: .. The primary antibody against p-MEK and p-ERK were used at a dilution of 1:1500 (Proteintech, 22734-1-AP), and staining was carried out following the UltraVision Quanto Detection System protocol (Thermo Fisher Scientific). ..

    Article Title: Radiomics-based prognostic model for progesterone resistance in endometrial cancer: insights into extracellular matrix and collagen type III
    Article Snippet: .. The primary antibody against COL III was used at a dilution of 1:1500 (Proteintech, 22734-1-AP), and staining was carried out following the UltraVision Quanto Detection System protocol (Thermo Fisher Scientific). ..



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    (A,B) Expression of α-SMA, <t>collagen</t> <t>III</t> in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.
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    (A,B) Expression of α-SMA, <t>collagen</t> <t>III</t> in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.
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    (A,B) Expression of α-SMA, <t>collagen</t> <t>III</t> in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.
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    (A,B) Expression of α-SMA, <t>collagen</t> <t>III</t> in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.
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    (A,B) Expression of α-SMA, <t>collagen</t> <t>III</t> in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.
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    Image Search Results


    (A,B) Expression of α-SMA, collagen III in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.

    Journal: Frontiers in Pharmacology

    Article Title: AP39 alleviates HHCY-induced myocardial remodeling by regulating FUNDC1-mediated mitochondrial dynamics via S-sulfhydration of NEDD8/CUL4B

    doi: 10.3389/fphar.2026.1729145

    Figure Lengend Snippet: (A,B) Expression of α-SMA, collagen III in the myocardial tissues of SD rats induced by HHCY in each group. (*p < 0.05 vs. Control, **p < 0.01 vs. Control; # p < 0.05 vs. HHCY; $$$ p < 0.005 vs. HHCY + AP39). (C) Relative expression of col1α2 and col3α1 genes in each group of SD rats as detected by QT-PCR. (D) Masson staining to detect the myocardial fiber conditions in the myocardial tissues of each group of SD rats (blue markers indicate myocardial fiber tissue). (E) Representative echocardiographic images of each group.

    Article Snippet: All primary antibodies used for Western blotting (WB) and immunofluorescence (IF) were purchased from the corresponding commercial suppliers, and their detailed information is listed as follows: GAPDH (Proteintech, USA; 10494-1-AP; WB 1:8000), α-smooth muscle actin (α-SMA) (Proteintech, USA; 14395-1-AP; WB 1:4000), Collagen type III (Proteintech, USA; 22734-1-AP; WB 1:800), FUNDC1 (Proteintech, China; AWA51295 ; IF 1:100, WB 1:1000), LC3B (Proteintech, USA; 14600-1-AP; IF 1:500, WB 1:4000), MFN1 (Proteintech, USA; 13798-1-AP; WB 1:5000), MFN2 (Proteintech, USA; 12186-1-AP; WB 1:20000), DRP1 (Proteintech, USA; 12957-1-AP; WB 1:5000), P53 (Proteintech, USA; 10442-1-AP; WB 1:20000), P16 (Proteintech, USA; 10883-1-AP; WB 1:3000), NEDD8 (Abways, China; AWA11003 ; WB 1:1000), and CUL4B (Abways, China; AWA48229 ; WB 1:1000).

    Techniques: Expressing, Control, Staining