A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Lipid-based in vivo transfection kit. Functionally tested in mice tissue-targeted delivery of siRNA and plasmid DNA via IV,IP,IT administrations. Kit includes: Cationic lipid-based reagent. Transfection Enhancer. Protocol for mice and rats. Uses: Transfection of DNA, RNA, protein and small molecules. Group: Life Science Research Product. Product ID: 5011.
The bifunctional enzyme from Escherichia coli transfers two 3-deoxy-D-manno-oct-2-ulosonate residues to lipid IVA (cf. EC 2.4.99.13 [(Kdo)-lipid IVA 3-deoxy-D-manno-octulosonic acid transferase]). The monofunctional enzymes from Aquifex aeolicus and Hemophilus influenzae catalyse the transfer of a single 3-deoxy-D-manno-oct-2-ulosonate residue from CMP-3-deoxy-D-manno-oct-2-ulosonate to lipid IVA. The enzymes from Chlamydia transfer three or more 3-deoxy-D-manno-oct-2-ulosonate residues and generate genus-specific epitopes. Group: Enzymes. Synonyms: KDO transferase; waaA (gene name); kdtA (gene name); 3-deoxy-D-manno-oct-2-ulosonic acid transferase; 3-deoxy-manno-octulosonic acid transferase; lipid IVA KDO transferase. Enzyme Commission Number: EC 2.4.99.12. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2696; lipid IVA 3-deoxy-D-manno-octulosonic acid transferase; EC 2.4.99.12; KDO transferase; waaA (gene name); kdtA (gene name); 3-deoxy-D-manno-oct-2-ulosonic acid transferase; 3-deoxy-manno-octulosonic acid transferase; lipid IVA KDO transferase. Cat No: EXWM-2696.
lipid IVA 4-amino-4-deoxy-L-arabinosyltransferase
Integral membrane protein present in the inner membrane of certain Gram negative endobacteria. In strains that do not produce 3-deoxy-D-manno-octulosonic acid (Kdo), the enzyme adds a single arabinose unit to the 1-phosphate moiety of the tetra-acylated lipid A precursor, lipid IVA. In the presence of a Kdo disaccharide, the enzyme primarily adds an arabinose unit to the 4-phosphate of lipid A molecules. The Salmonella typhimurium enzyme can add arabinose units to both positions. Group: Enzymes. Synonyms: undecaprenyl phosphate-α-L-Ara4N transferase; 4-amino-4-deoxy-L-arabinose lipid A transferase; polymyxin resistance protein PmrK; arnT (gene name). Enzyme Commission Number: EC 2.4.2.43. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2672; lipid IVA 4-amino-4-deoxy-L-arabinosyltransferase; EC 2.4.2.43; undecaprenyl phosphate-α-L-Ara4N transferase; 4-amino-4-deoxy-L-arabinose lipid A transferase; polymyxin resistance protein PmrK; arnT (gene name). Cat No: EXWM-2672.
lipid IVA palmitoyltransferase
Isolated from the bacteria Escherichia coli and Salmonella typhimurium. The enzyme prefers phosphatidylcholine with a palmitoyl group at the sn-1 position and palmitoyl or stearoyl groups at the sn-2 position. There is some activity with corresponding phosphatidylserines but only weak activity with other diacylphosphatidyl compounds. The enzyme also acts on Kdo-(2?4)-Kdo-(2?6)-lipid IVA. Group: Enzymes. Synonyms: PagP; crcA (gene name). Enzyme Commission Number: EC 2.3.1.251. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2201; lipid IVA palmitoyltransferase; EC 2.3.1.251; PagP; crcA (gene name). Cat No: EXWM-2201.
Lipid Metabolism Compound Library
A unique collection of 496 compounds targeting lipid metabolism, can be used for high-throughput screening (HTS) and high-content screening (HCS). - Covers several important targets, key components in lipid metabolism pathway, such as Acetyl-CoA Carboxylase?Acyltransferase?cholesteryl ester transfer protein (CETP)?FAAH?Fatty Acid Synthase (FASN)?HMG-CoA Reductase (HMGCR), etc. - Detailed compound information with structure, target, and biological activity description. - NMR and HPLC validated to ensure high purity and quality. Uses: Scientific use. Product Category: L2510. Categories: Lipid Metabolism Compounds Libraries.
Lipid mixture TLC-50, DHA glycerides. Group: Others. Purity: >99% (all components have a purity over 99%). Appearance: Powder. Storage: -20°C. Lipid mixture TLC-50, DHA glycerides; TLC; Mixed Lipid Mixtures; lipid mixture; mix; qualitive mixture; quantitive mixture; Matreya, LLC; Matyera; Larodan; lipid products. Cat No: LMIZ-080.
lipid-phosphate phosphatase
Requires Mg2+ for maximal activity. The enzyme from mammals is a bifunctional enzyme: the N-terminal domain exhibits lipid-phosphate-phosphatase activity and the C-terminal domain has the activity of EC 3.3.2.10, soluble epoxide hydrolase (sEH). The best substrates for this enzyme are 10-hydroxy-9-(phosphonooxy)octadecanoates, with the threo- form being a better substrate than the erythro- form. The phosphatase activity is not found in plant sEH or in EC 3.3.2.9, microsomal epoxide hydrolase, from mammals. Group: Enzymes. Synonyms: hydroxy fatty acid phosphatase; dihydroxy fatty acid phosphatase; hydroxy lipid phosphatase; sEH (ambiguous); soluble epoxide hydrolase (ambiguous). Enzyme Commission Number: EC 3.1.3.76. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3681; lipid-phosphate phosphatase; EC 3.1.3.76; hydroxy fatty acid phosphatase; dihydroxy fatty acid phosphatase; hydroxy lipid phosphatase; sEH (ambiguous); soluble epoxide hydrolase (ambiguous). Cat No: EXWM-3681.
Lipoamide
Lipoamide ((±)-α-Lipoamide) is a monocarboxylic acid derivative of a neutral amide, formed by the condensation of the carboxyl group of lipoic acid and ammonia. Lipoamide protects against oxidative stress-mediated neuronal cell damage and also acts as a coenzyme to transfer acetyl groups and hydrogen during pyruvate deacylation. Lipoamide also stimulates mitochondrial biogenesis in adipocytes through the endothelial NO synthase-cGMP-protein kinase G signaling pathway [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-α-Lipoamide; DL-Lipoamide; DL-6,8-Thioctamide. CAS No. 940-69-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B1142.
Lipoamide-PEG-Biotin, MW 1K-5K
Lipoamide-PEG-Biotin, MW 1,000 is a lipoic acid polyPEG which can bind to metallic surface through disulfide bond. The PEG derivative can be used for biotinylation due to its strong binding with avidin/streptavidin. Please contact us for GMP-grade inquiries.
lipoate-protein ligase
Requires Mg2+. This enzyme participates in lipoate salvage, and is responsible for lipoylation in the presence of exogenous lipoic acid. The enzyme attaches lipoic acid to the lipoyl domains of certain key enzymes involved in oxidative metabolism, including pyruvate dehydrogenase (E2 domain), 2-oxoglutarate dehydrogenase (E2 domain), the branched-chain 2-oxoacid dehydrogenases and the glycine cleavage system (H protein). Lipoylation is essential for the function of these enzymes. The enzyme can also use octanoate instead of lipoate. Group: Enzymes. Synonyms: lplA (gene name); lplJ (gene name); lipoate protein ligase; lipoate-protein ligase A; LPL; LPL-B. Enzyme Commission Number: EC 6.3.1.20. CAS No. 144114-18-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5723; lipoate-protein ligase; EC 6.3.1.20; 144114-18-1; lplA (gene name); lplJ (gene name); lipoate protein ligase; lipoate-protein ligase A; LPL; LPL-B. Cat No: EXWM-5723.
Lipocalin-2 human
recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy.
Lipofection 293-Adh (Liposome)
This product is a highly cost-effective and efficient transfection reagent based on innovative cationic liposomes, primarily designed for the adherent growth of HEK293, HEK293T, HEK293A, 293FT, and other cell lines within the HEK293 series. With a transfection efficiency of over 70% for the HEK293 cell series, it boasts low cytotoxicity, excellent reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection 293-Adh Pro (Liposome)
This product is an exceptionally efficient transfection reagent based on novel cationic liposomes, specifically designed for the adherent growth of HEK293, HEK293T, HEK293A, 293FT, and other cell lines within the HEK293 series. It is primarily used for high-efficiency transient transfection of plasmids, RNA, and oligonucleotides in the HEK293 cell series. With a transfection efficiency of up to 90% for the HEK293 cell series, it offers the advantages of low cytotoxicity, excellent reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection 293-Susp (Liposome)
This product is a highly efficient transfection reagent, based on cationic liposomes, designed specifically for transfecting plasmids and expressing recombinant proteins at high levels in suspension-cultured HEK293 cells. The transfection efficiency of this product can reach up to 85%, with excellent reproducibility, simple operation, and extremely low cytotoxicity. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection 293-Susp Pro (Liposome)
This product is a highly efficient transfection reagent, based on cationic liposomes, designed specifically for transfecting plasmids and expressing recombinant proteins at high levels in suspension-cultured HEK293 cells. The transfection efficiency of this product can reach up to 90%, with excellent reproducibility, simple operation, and extremely low cytotoxicity. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection Reagent Human Immune Cell (LNP)
This product is a universal transfection reagent based on LNPs, specifically designed for short-chain RNA transfection in human immune cells. It has the advantages of high transfection rate, low cytotoxicity, good reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection Reagent Mouse Immune Cell (LNP)
This product is a universal transfection reagent based on LNPs, specifically designed for short-chain RNA transfection in mouse immune cells. It has the advantages of high transfection rate, low cytotoxicity, good reproducibility, and simple operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofection Reagent-Universal (Liposome)
This product is an efficient transfection reagent based on liposomes, specifically designed for delivering plasmids, siRNA, or other forms of nucleic acids including DNA, RNA, oligonucleotides, as well as nucleic acid-protein complexes or negatively charged proteins into eukaryotic cells. It can also be used for nucleic acid transfection in live animals. Suitable for both adherent and suspension cells (such as HEK293T, Hela, NIH3T3, HEK293FT, CHO, etc.), it offers the advantages of low cytotoxicity, excellent reproducibility, and easy operation. Please note that it is intended for research purposes only and is not suitable for clinical diagnosis or treatment. Group: Transfection reagents.
Lipofermata
Lipofermata is a fatty acid transport protein 2 (FATP2) inhibitor. Lipofermata shows fatty acid transport inhibition with an IC50 of 4.84 ?M in Caco-2 cells. Lipofermata, an analog of spiro-indoline-thadiazole, shows zinc-specific suppression of antibacterial activity. Lipofermata perturbs zinc homeostasis in E. coli K-12 with a MIC of 16 ?M[1][2][3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 297180-15-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116788.
Lipohexin
It is produced by the strain of Moeszia lindtneri HKI-0054 Paecilomyces sp. HKI-0055 and HKI-0096. It's a peptide antibiotic. It has anti-gram-positive bacterial effect. It had competitive inhibitory effect on human placental proline endopeptidase with IC50 of 3.5 μmol/L. It inhibits the proline endopeptidase from the Flavobacterium meningoseptiu with IC50 of 25 μmol/L. Molecular formula: C39H68N6O9. Mole weight: 764.99.
Lipoic acid
Lipoic acid is a kind of B vitamins and can be used for the treatment of acute and chronic hepatitis, cirrhosis, hepatic coma, fatty liver, diabetes, etc. Alternative Names: 5-(dithiolan-3-yl)pentanoic acid;R-LIPOIC ACID POTASSIUM COMPOUND;6,8-Thioctic acid;6,8-Thiocticacid;6,8-Thiotic acid;6,8-Thioticacid. CAS No. 62-46-4. Product ID: PIPE-0268. Molecular formula: C8H14O2S2. Mole weight: 206.33. EINECS: 200-534-6. SMILES: C1CSSC1CCCCC(=O)O. Standard: USP. Category: Natural Extract.
Lipoic acid
Lipoic acid ((R)-(+)-α-Lipoic acid) is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. (R)-(+)-α-Lipoic acid is more effective than racemic Lipoic acid. Uses: Scientific research. Group: Natural products. Alternative Names: (R)-(+)-α-Lipoic acid; R-(+)-Thioctic acid. CAS No. 1200-22-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-18733.
Lipoic acid, reduced
Lipoic acid, reduced. Group: Biochemicals. Alternative Names: (±)-6,8-Dimercaptooctanoic acid; (±)-Dihydrolipoic acid. Grades: Highly Purified. CAS No. 462-20-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C8H16O2S2. US Biological Life Sciences.
Worldwide
Lipoic Acid (Thioctic Acid, Alpha Lipoic Acid)
Coenzyme in the oxidative decarboxylation reactions of glucose metabolism and the citric acid cycle. Although it is an essential growth factor for various micro-organisms. a-Lipoic acid, is a naturally occuring coenzyme containing a disulfide that has been used to treat polyneuropathies and hepatic disorders. a-Lipoic acid is a potent inhibitor of NFKB activation and HIV-1 tat driven gene expression. Group: Biochemicals. Alternative Names: (+/-)-1,2-Dithiolane-3-pentanoic Acid; (+/-)-1,2-Dithiolane-3-valeric Acid; (+/-)-Thioctic Acid; (RS)-α-Lipoic Acid; DL-Thioctic Acid; Liposan; Lipothion; NSC 628502; NSC 90788; Protogen A; Thioctsan; Tioctacid. Grades: Cell Culture Grade. CAS No. 1077-28-7. Pack Sizes: 10g, 25g, 100g, 500g. Molecular Formula: C8H14O2S2, Molecular Weight: 206.3. US Biological Life Sciences.
Worldwide
Lipomycin α
It is produced by the strain of Str. aureofaciens Tu117. It has strong activity of anti-gram-positive bacterial and no activity against fungi (including yeast). Synonyms: alpha-Lipomycin; 4-[13-[(2,6-Dideoxy-beta-D-ribo-hexopyranosyl)oxy]-10,12,14-trimethyl-1-oxopentadeca-2,4,6,8,10-pentenyl]-2,5-dihydro-3-hydroxy-1-methyl-5-oxo-1H-pyrrole-2-propanoic acid. Grade: >95% by HPLC. CAS No. 51053-40-8. Molecular formula: C32H45NO9. Mole weight: 587.70.
Lipomycin β
It is produced by the strain of Str. aureofaciens Tu117. It has the activity of anti-gram-positive bacterial and no activity against fungi (including yeast). Synonyms: beta-Lipomycin; 2,5-Dihydro-3-hydroxy-4-(13-hydroxy-10,12,14-trimethyl-1-oxo-2,4,6,8,10-pentadecapentenyl)-1-methyl-5-oxo-1H-pyrrole-2-propanoic acid. CAS No. 51053-41-9. Molecular formula: C26H35NO6. Mole weight: 457.56.
lipopolysaccharide 3-α-galactosyltransferase
Transfers α-D-galactosyl residues to D-glucose in the partially completed core of lipopolysaccharide [cf. EC 2.4.1.56 (lipopolysaccharide N-acetylglucosaminyltransferase), EC 2.4.1.58 (lipopolysaccharide glucosyltransferase I) and EC 2.4.1.73 (lipopolysaccharide glucosyltransferase II)]. Group: Enzymes. Synonyms: UDP-galactose:lipopolysaccharide α,3-galactosyltransferase; UDP-galactose:polysaccharide galactosyltransferase; uridine diphosphate galactose:lipopolysaccharide α-3-galactosyltransferase; uridine diphosphogalactose-lipopolysaccharide α,3-galactosyltransferase; UDP-galactose:lipopolysaccharide 3-α-D-galactosyltransferase. Enzyme Commission Number: EC 2.4.1.44. CAS No. 9073-98-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2590; lipopolysaccharide 3-α-galactosyltransferase; EC 2.4.1.44; 9073-98-7; UDP-galactose:lipopolysaccharide α,3-galactosyltransferase; UDP-galactose:polysaccharide galactosyltransferase; uridine diphosphate galactose:lipopolysaccharide α-3-galactosyltransferase; uridine diphosphogalactose-lipopolysaccharide α,3-galactosyltransferase; UDP-galactose:lipopolysaccharide 3-α-D-galactosyltransferase. Cat No: EXWM-2590.
Lipopolysaccharide from Porphyromonas gingivalis
purified by phenol extraction. Group: Polysaccharide.
Lipopolysaccharide from Porphyromonas gingivalis
Lipopolysaccharide from Porphyromonas gingivalis. Group: Polysaccharide.
lipopolysaccharide glucosyltransferase I
Transfers glucosyl residues to the backbone portion of lipopolysaccharide [cf. EC 2.4.1.44 (lipopolysaccharide 3-α-galactosyltransferase, EC 2.4.1.56 (lipopolysaccharide N-acetylglucosaminyltransferase) and EC 2.4.1.73 (lipopolysaccharide glucosyltransferase II)]. Group: Enzymes. Synonyms: UDP-glucose:lipopolysaccharide glucosyltransferase I; lipopolysaccharide glucosyltransferase; uridine diphosphate glucose:lipopolysaccharide glucosyltransferase I; uridine diphosphoglucose-lipopolysaccharide glucosyltransferase. Enzyme Commission Number: EC 2.4.1.58. CAS No. 9074-00-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2603; lipopolysaccharide glucosyltransferase I; EC 2.4.1.58; 9074-00-4; UDP-glucose:lipopolysaccharide glucosyltransferase I; lipopolysaccharide glucosyltransferase; uridine diphosphate glucose:lipopolysaccharide glucosyltransferase I; uridine diphosphoglucose-lipopolysaccharide glucosyltransferase. Cat No: EXWM-2603.
lipopolysaccharide glucosyltransferase II
Transfers glucosyl residues to the D-galactosyl-D-glucosyl side-chains in the partially completed core of lipopolysaccharides. cf. EC 2.4.1.44 (lipopolysaccharide 3-α-galactosyltransferase), EC 2.4.1.56 (lipopolysaccharide N-acetylglucosaminyltransferase) and EC 2.4.1.58 (lipopolysaccharide glucosyltransferase I). Group: Enzymes. Synonyms: uridine diphosphoglucose-galactosylpolysaccharide glucosyltransferase. Enzyme Commission Number: EC 2.4.1.73. CAS No. 51004-27-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2616; lipopolysaccharide glucosyltransferase II; EC 2.4.1.73; 51004-27-4; uridine diphosphoglucose-galactosylpolysaccharide glucosyltransferase. Cat No: EXWM-2616.
Transfers N-acetylglucosaminyl residues to a D-galactose residue in the partially completed lipopolysaccharide core [cf. EC 2.4.1.44 (lipopolysaccharide 3-α-galactosyltransferase), EC 2.4.1.58 (lipopolysaccharide glucosyltransferase I) and EC 2.4.1.73 (lipopolysaccharide glucosyltransferase II)]. Group: Enzymes. Synonyms: UDP-N-acetylglucosamine-lipopolysaccharide N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-lipopolysaccharide acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:lipopolysaccharide N-acetyl-D-glucosaminyltransferase. Enzyme Commission Number: EC 2.4.1.56. CAS No. 37277-64-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2601; lipopolysaccharide N-acetylglucosaminyltransferase; EC 2.4.1.56; 37277-64-8; UDP-N-acetylglucosamine-lipopolysaccharide N-acetylglucosaminyltransferase; uridine diphosphoacetylglucosamine-lipopolysaccharide acetylglucosaminyltransferase; UDP-N-acetyl-D-glucosamine:lipopolysaccharide N-acetyl-D-glucosaminyltransferase. Cat No: EXWM-2601.
Involved in the biosynthesis of common antigen in Enterobacteriaceae. Group: Enzymes. Synonyms: ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Enzyme Commission Number: EC 2.4.1.180. CAS No. 113478-30-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2406; lipopolysaccharide N-acetyl mannosaminouronosyl transferase; EC 2.4.1.180; 113478-30-1; ManNAcA transferase; uridine diphosphoacetyl mannosaminuronate-acetyl glucosaminyl pyrophosphoryl undecaprenol acetylmannosaminuronosyltransferase; UDP-N-acetyl-β-D-mannosaminouronate:lipid I N-acetyl-β-D-mannosaminouronosyltransferase (incorrect). Cat No: EXWM-2406.
Lipopolysaccharides
Lipopolysaccharides Inhibitor. Uses: Scientific use. Product Category: T11855. CAS No.:
Lipopolysaccharides, from E. coli O111:B4
Lipopolysaccharides, from E. coli O111:B4 (LPS, from Escherichia coli (O111:B4)) are endotoxins and TLR4 activators extracted from Escherichia coli (E. coli O111:B4) and are classified as S (smooth) type LPS. Lipopolysaccharides (LPS), from E. coli O111:B4 possess the typical three-part structure: O-antigen, R3-type core oligosaccharide, and lipid A. Lipopolysaccharides (LPS), from E. coli O111:B4 activate TLR-4 in immune cells and can cause significant gastric diseases. Lipopolysaccharides (LPS), from E. coli O111:B4 can be used to induce cellular inflammation and establish animal models related to inflammation[1][2][3][4][5][6][7][8][9].It is recommended to prepare a stock solution of ?2 mg/mL and ensure that it is fully mixed and dissolved. Due to the adsorption characteristics of LPS, low adsorption centrifuge tubes should be used for aliquoting and storage. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: LPS, from Escherichia coli (O111:B4). Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-D1056A1.
Lipopolysaccharides, from E. coli O55:B5
Lipopolysaccharides, from E. coli O55:B5 (LPS, from Escherichia coli (O55:B5)) are endotoxins and TLR4 activators extracted from Escherichia coli (E. coli O55:B5) and are classified as S (smooth) type LPS. Lipopolysaccharides, from E. coli O55:B5 possess the typical three-part structure: O-antigen, core oligosaccharide, and lipid A. Lipopolysaccharides, from E. coli O55:B5 activate TLR-4 in immune cells, exhibit high pyrogenicity, and demonstrate dose and serotype specificity. Lipopolysaccharides, from E. coli O55:B5 can be used to induce cellular inflammation and establish animal models related to inflammation[1][2][3][4][5][6][7]. It is recommended to prepare a stock solution of ?2 mg/mL. Vortex thoroughly for more than 10 minutes. Due to the adsorption characteristics of LPS, low adsorption centrifuge tubes should be used for aliquoting and storage. Uses: Scientific research. Group: Natural products. Alternative Names: LPS. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-D1056.
Lipopolysaccharides from Escherichia coli
Lipopolysaccharides produced by Escherichia coli are endotoxins. Synonyms: Lipopolysaccharide E. Coli; Escherichia coli lipopolysaccharides; Lipopolysaccharides, Escherichiacoli; Citopyros; Escherichia coli lipopolysaccharide; Lipopolysaccharide, Escherichia coli; Lipopolysaccharides, Escherichia coli. CAS No. 93572-42-0.
Lipopolysaccharides from Escherichia coli K-235
Lipopolysaccharides from Escherichia coli K-235. Group: Polysaccharide.