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Abmart Inc primary antibodies against p16
Primary Antibodies Against P16, supplied by Abmart Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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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).
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Abmart Inc primary antibodies against 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).
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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).
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Cell Signaling Technology Inc primary antibodies against 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).
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Proteintech primary antibodies against p16 proteintech 10883-1-ap
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).
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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