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LPS, from bacterial (Proteus vulgaris)

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Toll-like Receptor (TLR) (1)
By Research Areas:	Inflammation/Immunology (1)

Targets Recommended: Bacterial

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-D1056B1

Lipopolysaccharides, from Proteus vulgaris LPS, from bacterial (Proteus vulgaris)	Toll-like Receptor (TLR)	Inflammation/Immunology
Lipopolysaccharides, from Proteus vulgaris are lipopolysaccharide endotoxins and TLR-4 activators derived from Proteus vulgaris, classified as S-type LPS, which can activate pathogen-associated molecular patterns (PAMP) of the immune system and induce cellular secretion of migrasomes. Lipopolysaccharides, from Proteus vulgaris exhibit a typical three-part structure: O-antigen, core oligosaccharide, and lipid A. Lipopolysaccharides, from Proteus vulgaris possess a unique molecular structure and chitosan affinity (K_b=2.72 μM), surpassing that of Yersinia pseudotuberculosis (K_b=6.06 μM) and Escherichia coli (K_b=79.50 μM) .

Cat. No.	Product Name	Type

HY-D1056B1

Lipopolysaccharides, from Proteus vulgaris LPS, from bacterial (Proteus vulgaris)	Carbohydrates
Lipopolysaccharides, from Proteus vulgaris are lipopolysaccharide endotoxins and TLR-4 activators derived from Proteus vulgaris, classified as S-type LPS, which can activate pathogen-associated molecular patterns (PAMP) of the immune system and induce cellular secretion of migrasomes. Lipopolysaccharides, from Proteus vulgaris exhibit a typical three-part structure: O-antigen, core oligosaccharide, and lipid A. Lipopolysaccharides, from Proteus vulgaris possess a unique molecular structure and chitosan affinity (K_b=2.72 μM), surpassing that of Yersinia pseudotuberculosis (K_b=6.06 μM) and Escherichia coli (K_b=79.50 μM) .

Lipopolysaccharides, from Proteus vulgaris

LPS, from bacterial (Proteus vulgaris)

Carbohydrates

Lipopolysaccharides, from Proteus vulgaris are lipopolysaccharide endotoxins and TLR-4 activators derived from Proteus vulgaris, classified as S-type LPS, which can activate pathogen-associated molecular patterns (PAMP) of the immune system and induce cellular secretion of migrasomes. Lipopolysaccharides, from Proteus vulgaris exhibit a typical three-part structure: O-antigen, core oligosaccharide, and lipid A. Lipopolysaccharides, from Proteus vulgaris possess a unique molecular structure and chitosan affinity (K_b=2.72 μM), surpassing that of Yersinia pseudotuberculosis (K_b=6.06 μM) and Escherichia coli (K_b=79.50 μM) .

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LPS, from bacterial (Proteus vulgaris)

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