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rabbit polyclonal anti col2 primary antibodies  (Bioss)


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    Bioss rabbit polyclonal anti col2 primary antibodies
    List of antibodies used in western blotting.
    Rabbit Polyclonal Anti Col2 Primary Antibodies, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti col2 primary antibodies/product/Bioss
    Average 94 stars, based on 14 article reviews
    rabbit polyclonal anti col2 primary antibodies - by Bioz Stars, 2026-03
    94/100 stars

    Images

    1) Product Images from "Platelet-rich plasma protects rat chondrocytes from interleukin-1β-induced apoptosis"

    Article Title: Platelet-rich plasma protects rat chondrocytes from interleukin-1β-induced apoptosis

    Journal: Molecular Medicine Reports

    doi: 10.3892/mmr.2016.5767

    List of antibodies used in western blotting.
    Figure Legend Snippet: List of antibodies used in western blotting.

    Techniques Used: Western Blot

    Platelet-rich plasma (PRP) inhibits the expression of catabolic genes induced by interleukin (IL)-1β. (A) Quantitative polymerase chain reaction was performed 24 h following treatment of chondrocytes (N=3). (B) Western blotting detected downregulation of matrix metalloproteinases (MMPs), and upregulation of tissue inhibitor of metalloproteinases (TIMP), SRY-box 9 (SOX9) and collagen type II (COL2) in the IL-1β + PRP group compared with the IL-1β group. (C) Semi-quantification of blots confirmed the expression of anabolic proteins was increased by PRP (N=3). *P<0.05, vs. the IL-1β group. GAPDH, glyceraldehyde 3-phosphate dehydrogenase.
    Figure Legend Snippet: Platelet-rich plasma (PRP) inhibits the expression of catabolic genes induced by interleukin (IL)-1β. (A) Quantitative polymerase chain reaction was performed 24 h following treatment of chondrocytes (N=3). (B) Western blotting detected downregulation of matrix metalloproteinases (MMPs), and upregulation of tissue inhibitor of metalloproteinases (TIMP), SRY-box 9 (SOX9) and collagen type II (COL2) in the IL-1β + PRP group compared with the IL-1β group. (C) Semi-quantification of blots confirmed the expression of anabolic proteins was increased by PRP (N=3). *P<0.05, vs. the IL-1β group. GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Techniques Used: Expressing, Real-time Polymerase Chain Reaction, Western Blot



    Similar Products

    rabbit polyclonal anti col2 primary antibodies  (Bioss)
    94
    Bioss rabbit polyclonal anti col2 primary antibodies
    List of antibodies used in western blotting.
    Rabbit Polyclonal Anti Col2 Primary Antibodies, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti col2 primary antibodies/product/Bioss
    Average 94 stars, based on 1 article reviews
    rabbit polyclonal anti col2 primary antibodies - by Bioz Stars, 2026-03
    94/100 stars
    		  Buy from Supplier

    Image Search Results


    List of antibodies used in western blotting.

    Journal: Molecular Medicine Reports

    Article Title: Platelet-rich plasma protects rat chondrocytes from interleukin-1β-induced apoptosis

    doi: 10.3892/mmr.2016.5767

    Figure Lengend Snippet: List of antibodies used in western blotting.

    Article Snippet: Permeabilization and blocking were performed by incubating the cells with 1% Triton-X 100 and 1% bovine serum albumin for 15 min. Cover slips were then incubated overnight at 4°C with rabbit polyclonal anti-COL2 primary antibodies (cat. no. Bs-11929R; dilution, 1:500; Bioss, Inc., Woburn, MA, USA).

    Techniques: Western Blot

    Platelet-rich plasma (PRP) inhibits the expression of catabolic genes induced by interleukin (IL)-1β. (A) Quantitative polymerase chain reaction was performed 24 h following treatment of chondrocytes (N=3). (B) Western blotting detected downregulation of matrix metalloproteinases (MMPs), and upregulation of tissue inhibitor of metalloproteinases (TIMP), SRY-box 9 (SOX9) and collagen type II (COL2) in the IL-1β + PRP group compared with the IL-1β group. (C) Semi-quantification of blots confirmed the expression of anabolic proteins was increased by PRP (N=3). *P<0.05, vs. the IL-1β group. GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Journal: Molecular Medicine Reports

    Article Title: Platelet-rich plasma protects rat chondrocytes from interleukin-1β-induced apoptosis

    doi: 10.3892/mmr.2016.5767

    Figure Lengend Snippet: Platelet-rich plasma (PRP) inhibits the expression of catabolic genes induced by interleukin (IL)-1β. (A) Quantitative polymerase chain reaction was performed 24 h following treatment of chondrocytes (N=3). (B) Western blotting detected downregulation of matrix metalloproteinases (MMPs), and upregulation of tissue inhibitor of metalloproteinases (TIMP), SRY-box 9 (SOX9) and collagen type II (COL2) in the IL-1β + PRP group compared with the IL-1β group. (C) Semi-quantification of blots confirmed the expression of anabolic proteins was increased by PRP (N=3). *P<0.05, vs. the IL-1β group. GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Article Snippet: Permeabilization and blocking were performed by incubating the cells with 1% Triton-X 100 and 1% bovine serum albumin for 15 min. Cover slips were then incubated overnight at 4°C with rabbit polyclonal anti-COL2 primary antibodies (cat. no. Bs-11929R; dilution, 1:500; Bioss, Inc., Woburn, MA, USA).

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Western Blot