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Porphyromonas gingivalis lipopolysaccharide lps pg

Manufactured by InvivoGen
Sourced in United States

Porphyromonas gingivalis lipopolysaccharide (LPS-Pg) is a purified bacterial endotoxin derived from the Gram-negative anaerobic bacterium Porphyromonas gingivalis. It is a key component of the bacterial cell wall and plays a crucial role in the host-pathogen interaction.

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3 protocols using porphyromonas gingivalis lipopolysaccharide lps pg

1

Rabbit Model of Periodontitis

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Agents: Glycerol monooleate (GMO, DIMODAN®MO/D KOSHER) was a present from Danisco Cultor (Brabrand, Denmark). N-methyl pyrrolidone (NMP) was purchased from Guangfu Smart Chemical Research Institute (Tianjin, China). Medium chain triglyceride (MCT) was purchased from Gracia Chemical Technology Co., Ltd. (Chengdu, China). Metronidazole (MTZ) was obtained from Huanggang SaiKang Pharmacy Co., Ltd. (purity ≥99.0%, Huanggang, China). MTZ tablets were produced by Kangmei Pharmaceutical Co., Ltd. (Jieyang, China). Ligature suture (3–0) was purchased from Johnson & Johnson Medical Ltd. (Shanghai, China). Porphyromonas gingivalis lipopolysaccharide (LPS-PG) and pentobarbital sodium were obtained from Invivogen (San Diego, CA) and Sigma (Shanghai, China), respectively. All other chemicals were of analytical grade and used as received.
Animals: New Zealand rabbits, 10 weeks old, weighing approximately 3.0 kg, were purchased from the Laboratory Animal Center of Sun Yat-sen University (Guangzhou, China). Studies were conducted in accordance with guidelines and procedures approved by the Institutional Authority for Laboratory Animal Care and Ethics Committee of Sun Yat-sen University.
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2

Investigating Cell Viability with LPS-Pg, zVAD, and Nec-1

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Cells were seeded into 96-well plates and treated with 1 µg/mL Porphyromonas gingivalis lipopolysaccharide (LPS-Pg; InvivoGen, San Diego, CA, USA), 20 µM of the pan-caspase inhibitor, zVAD (Promega, Madison, WI, USA) or 30 µM Nec-1 (Cambridge Bioscience, Cambridge, UK) for 24 h. Cell survival was determined using the CellTiter-Glo luminescent cell viability assay (Promega). Luminescence was read using an In nite M200 microplate reader (Tecan, Zürich, Switzerland).
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3

Investigating Cell Viability with LPS-Pg, zVAD, and Nec-1

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Cells were seeded into 96-well plates and treated with 1 µg/mL Porphyromonas gingivalis lipopolysaccharide (LPS-Pg; InvivoGen, San Diego, CA, USA), 20 µM of the pan-caspase inhibitor, zVAD (Promega, Madison, WI, USA) or 30 µM Nec-1 (Cambridge Bioscience, Cambridge, UK) for 24 h. Cell survival was determined using the CellTiter-Glo luminescent cell viability assay (Promega). Luminescence was read using an In nite M200 microplate reader (Tecan, Zürich, Switzerland).
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