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primary antibodies against cell senescence marker p16  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc primary antibodies against cell senescence marker p16
    Flammulina velutipes polysaccharides (FVP) attenuated cell <t>senescence</t> triggered by advanced glycation end products (AGEs) and lipopolysaccharide (LPS)-treated human gingival fibroblasts (HGFs). Senescence-associated β-galactosidase (SA-β-gal) activity was measured in HGFs pretreated with AGEs and LPS, followed by the addition of FVP (A). The protein level of senescence marker <t>p16</t> was determined by Western blot under the same treatment conditions (B).
    Primary Antibodies Against Cell Senescence Marker P16, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/primary+antibodies+against+p16/pmc12485397-59-0-11?v=Cell+Signaling+Technology+Inc
    Average 86 stars, based on 1 article reviews
    primary antibodies against cell senescence marker p16 - by Bioz Stars, 2026-07
    86/100 stars

    Images

    1) Product Images from "Flammulina velutipes polysaccharides exhibit potent antioxidant and anti-pyroptotic properties in diabetes-associated periodontitis: A preliminary in vitro study"

    Article Title: Flammulina velutipes polysaccharides exhibit potent antioxidant and anti-pyroptotic properties in diabetes-associated periodontitis: A preliminary in vitro study

    Journal: Journal of Dental Sciences

    doi: 10.1016/j.jds.2025.07.017

    Flammulina velutipes polysaccharides (FVP) attenuated cell senescence triggered by advanced glycation end products (AGEs) and lipopolysaccharide (LPS)-treated human gingival fibroblasts (HGFs). Senescence-associated β-galactosidase (SA-β-gal) activity was measured in HGFs pretreated with AGEs and LPS, followed by the addition of FVP (A). The protein level of senescence marker p16 was determined by Western blot under the same treatment conditions (B).
    Figure Legend Snippet: Flammulina velutipes polysaccharides (FVP) attenuated cell senescence triggered by advanced glycation end products (AGEs) and lipopolysaccharide (LPS)-treated human gingival fibroblasts (HGFs). Senescence-associated β-galactosidase (SA-β-gal) activity was measured in HGFs pretreated with AGEs and LPS, followed by the addition of FVP (A). The protein level of senescence marker p16 was determined by Western blot under the same treatment conditions (B).

    Techniques Used: Activity Assay, Marker, Western Blot



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    Image Search Results


    Flammulina velutipes polysaccharides (FVP) attenuated cell senescence triggered by advanced glycation end products (AGEs) and lipopolysaccharide (LPS)-treated human gingival fibroblasts (HGFs). Senescence-associated β-galactosidase (SA-β-gal) activity was measured in HGFs pretreated with AGEs and LPS, followed by the addition of FVP (A). The protein level of senescence marker p16 was determined by Western blot under the same treatment conditions (B).

    Journal: Journal of Dental Sciences

    Article Title: Flammulina velutipes polysaccharides exhibit potent antioxidant and anti-pyroptotic properties in diabetes-associated periodontitis: A preliminary in vitro study

    doi: 10.1016/j.jds.2025.07.017

    Figure Lengend Snippet: Flammulina velutipes polysaccharides (FVP) attenuated cell senescence triggered by advanced glycation end products (AGEs) and lipopolysaccharide (LPS)-treated human gingival fibroblasts (HGFs). Senescence-associated β-galactosidase (SA-β-gal) activity was measured in HGFs pretreated with AGEs and LPS, followed by the addition of FVP (A). The protein level of senescence marker p16 was determined by Western blot under the same treatment conditions (B).

    Article Snippet: Primary antibodies against cell senescence marker p16 and pyroptosis markers ASC (Cell Signaling Inc., Danvers, MA, USA), NLRP3 (Invitrogen Life Technologies, Carlsbad, CA, USA), pro-caspase-1 and cleaved caspase-1 (Abcam, Cambridge, UK), pro-GSDMD and cleaved GSDMD (Cell signaling), pro-IL-1β and IL-1β (Cell signaling), and GAPDH (Invitrogen) were used.

    Techniques: Activity Assay, Marker, Western Blot