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Lipopolysaccharides, from Proteus mirabilis
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Catalog No. TSW-00844
Alias LPS, from bacterial (Proteus mirabilis), Lipopolysaccharides (from Proteus mirabilis)
Lipopolysaccharides, fromProteus mirabilis, are endotoxins derived from the bacterium Proteus mirabilis, functioning as TLR-4 activators and featuring an S-type LPS structure. They play a role in activating pathogen-associated molecular patterns (PAMP) and inducing cell-extracellular vesicle release. These lipopolysaccharides have a classic tripartite structure: O antigen, core oligosaccharide, and lipid A. Proteus mirabilis is a primary pathogen responsible for urinary tract infections and has potential links to rheumatoid arthritis. Additionally, Lipopolysaccharides, fromProteus mirabilis, exhibit promising antitumor effects, showing in vivo inhibitory activity against solid tumors such as meningeal sarcoma and Walker carcinoma.
Lipopolysaccharides, from Proteus mirabilis
Lipopolysaccharides, from Proteus mirabilis
😃Good
Catalog No. TSW-00844Alias LPS, from bacterial (Proteus mirabilis), Lipopolysaccharides (from Proteus mirabilis)
Lipopolysaccharides, fromProteus mirabilis, are endotoxins derived from the bacterium Proteus mirabilis, functioning as TLR-4 activators and featuring an S-type LPS structure. They play a role in activating pathogen-associated molecular patterns (PAMP) and inducing cell-extracellular vesicle release. These lipopolysaccharides have a classic tripartite structure: O antigen, core oligosaccharide, and lipid A. Proteus mirabilis is a primary pathogen responsible for urinary tract infections and has potential links to rheumatoid arthritis. Additionally, Lipopolysaccharides, fromProteus mirabilis, exhibit promising antitumor effects, showing in vivo inhibitory activity against solid tumors such as meningeal sarcoma and Walker carcinoma.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 50 mg | Inquiry | Inquiry | Inquiry | |
| 100 mg | Inquiry | Inquiry | Inquiry | |
| 250 mg | Inquiry | Inquiry | Inquiry |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Chemical Properties
Storage & Solubility Information
| Description | Lipopolysaccharides, fromProteus mirabilis, are endotoxins derived from the bacterium Proteus mirabilis, functioning as TLR-4 activators and featuring an S-type LPS structure. They play a role in activating pathogen-associated molecular patterns (PAMP) and inducing cell-extracellular vesicle release. These lipopolysaccharides have a classic tripartite structure: O antigen, core oligosaccharide, and lipid A. Proteus mirabilis is a primary pathogen responsible for urinary tract infections and has potential links to rheumatoid arthritis. Additionally, Lipopolysaccharides, fromProteus mirabilis, exhibit promising antitumor effects, showing in vivo inhibitory activity against solid tumors such as meningeal sarcoma and Walker carcinoma. |
| Synonyms | LPS, from bacterial (Proteus mirabilis), Lipopolysaccharides (from Proteus mirabilis) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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