This is a Validated Antibody Database (VAD) review about LPS, based on 33 published articles (read how Labome selects the articles), using LPS product in experiments. It is aimed to help Labome visitors find the most suited LPS. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
synonym: LPS

Axxora LPS was used to perform LPS treatment in order to show that migration of lymphocytes from blood to lymphoid tissues needs GRK2-dependent S1PR1 desensitization to the paper
InvitrogenInvitrogen LPS product
Invitrogen LPS was used in 1 ug/mL to perform stimulation experiments in order to show that different stimulation effect of human hematopoietic cells could be analysized by single-cell mass cytometry to the paper
Enzo Life Sciences
Alexis Biochemicals LPS was used in 20ug/ml to perform cell stimulation in order to show that antigen presentation capacity is affected by asymmetric segregation of polarized antigen on B cell division to the paper
Enzo Life Sciences Donkey LPS was used to perform activating experiments in order to show that Salmonella enterica growth was restricted by phosphorylation of autophagy receptor optineurin to the paper
Abcam
Mouse monoclonal anti-Salmonella LPS antibody was used in immunofluorescence detection in macrophages in order to study the acid-dependent secretion process during Salmonella macrophage infection to the paper
R&D Systems
R&D Systems LPS was used to stimulate B cells in order to investigate the role of Pol in DNA DSB repair to the paper
MilliporeSigma
Sigma-Aldrich LPS was used to perform cell culture to study the effect of mast cells with A20 deficiency on inflammatory responses to the paper
Sigma LPS was used to perform blocking or activation experiments in order to investigate the importance of TCR signaling to natural killer T cell development to the paper
Sigma LPS was used to perform cell stimulation in order to show that protein could be synthesized using CUG as start codons to provide peptides for MHC class I to the paper
Sigma LPS was used to perform LPS binding assay in order to show that intestinal microbiota is essential for mouse mammary tumor virus infection in mice to the paper
Sigma LPS was used in 10 mg/kg to perform mouse stimulation in order to show that vagus nerve circuit could inhibit cytokine production through acetylcholine-producing T cells in spleen to the paper
Sigma LPS was used to stimulate cultured pDCs in order to investigate the role for adaptor protein 3 in the regulation Toll-like receptor 9 signaling to the paper
Sigma LPS was used to perform cell culture in order to study the mechanism of A20 action in the inhibition of NF-kappaB signaling to the paper
Sigma LPS was used to add to medium in order to study the role for TRAF6 in T cell-dependent and T cell-independent humoral immune responses to the paper
Sigma LPS was used to treat the cellls in order to illustrate the function of tomato lycopene extract in preventing LPS-induced proinflammatory gene expression and aggravating DSS-induced colitis to the paper
Sigma Aldrich LPS (O55:B5) was used to treat cells in order to study the role for IL-32 in the effect of IL-1 on endothelial cell functions to the paper
Sigma-Aldrich LPS was used to inject B6 or IL-6 KO mice in order to indicate a pathogenic role of Th17 cells via IL-17 in persistent viral infection and chronic inflammatory diseases to the paper
Sigma LPS was used to perform TLR stimulation experiments in order to show that the cyclin dependent kinase domain of p21 can inhibit IL-1-mediated inflammation to the paper
Sigma LPS was used to perform stimulation in order to reveal that Tlr9 and the Nalp3 inflammasome are the two signals required in acetaminophen-induced hepatotoxicity to the paper
Sigma-Aldrich LPS was used to activate the CD4+ T cells in order to demonstrate IL-6 promotes antibody production through increased IL-21 production to the paper
Sigma LPS was used to stimulate the reaction mixtures containing U937 cells in order to evaluate the potential relevance of ApoER2 for APC cell signaling mechanisms to the paper
Sigma-Aldrich LPS was used to treat cells in order to study the expression of albumin in human microglial cells and brain tissues to the paper
Sigma LPS was used to activate cells in order to study the effect of TCDD on B cell differentiation in dysregulation of paired Box 5 (Pax5) isoform, Pax5a to the paper
Sigma-Aldrich 10 g/kg LPS was used in intraperitoneal injection of mice to conduct in vivo stimulation experiments in order to study the trans presentation mechanism which could activate NK cells by dendritic cell membrane complexes composed with IL-15Ralpha chaperones IL-15 to the paper
Sigma LPS was used to be as a positive control stimulus for TNF-alpha production in order to investigate the function of SpvC to the paper
Sigma-Aldrich LPS (Escherichia coli 0127:B8) was used to stimulate cells in order to study the roles for mitogen-activated protein kinases and NFkappaB in LPS-induced CD40 expression on human monocytic cells to the paper
InvivoGen
Invivogen LPS was used to stimulate T cells in order to investigate the effect of TCR/pMHC interaction parameters on T cell responses in vivo to the paper
InvivoGen LPS was used to perform adhesion-dependent activation in order to show that PLCgamma2 is an important player in integrin and Fc receptor-mediated neutrophil functions and the neutrophil-mediated effector phase of autoimmune arthritis to the paper
InvivoGen LPS was used in flow cytometry in order to indicate that the contrasting roles for all-trans retinoic acid in TGF-mediated induction of Foxp3 and Il10 genes in developing regulatory T cells to the paper
InVivoGen LPS (TLR4-specific) was used to injected into the corneal stroma for constructing murine model of corneal inflammation in order to study the roles of MMP-8 and MMP-9 in a neutrophil-dependent inflammatory response to the paper
Hycult Biotech
Hycult mouse anti-LPS core (clone WN1 222-5) antibody was used to perform immunohistochemistry in order to shown that in the absence of SIV infection, PTM have damage to their gastrointestinal tract and increased basal levels of microbial translocation and immune activation to the paper
HyCult Biotechnology LPS was used to analyze serum samples in serum determinations in order to research the role of MMP-8 in Porphyromonas gingivalis-induced periodontitis to the paper
BD Biosciences
Difco anti-LPS was used to perform immunocytochemistry in order to show that mucosal innate immunity could be promoted by HD6 self-assembly to the paper
Articles Reviewed
  1. Chakraborty S, Mizusaki H, Kenney L. A FRET-based DNA biosensor tracks OmpR-dependent acidification of Salmonella during macrophage infection. PLoS Biol. 2015;13:e1002116 pubmed publisher
  2. Heger K, Fierens K, Vahl J, Aszodi A, Peschke K, Schenten D, et al. A20-deficient mast cells exacerbate inflammatory responses in vivo. PLoS Biol. 2014;12:e1001762 pubmed publisher
  3. Vahl J, Heger K, Knies N, Hein M, Boon L, Yagita H, et al. NKT cell-TCR expression activates conventional T cells in vivo, but is largely dispensable for mature NKT cell biology. PLoS Biol. 2013;11:e1001589 pubmed publisher
  4. Starck S, Jiang V, PAVON ETERNOD M, Prasad S, McCarthy B, Pan T, et al. Leucine-tRNA initiates at CUG start codons for protein synthesis and presentation by MHC class I. Science. 2012;336:1719-23 pubmed publisher
  5. Chu H, Pazgier M, Jung G, Nuccio S, Castillo P, de Jong M, et al. Human ?-defensin 6 promotes mucosal innate immunity through self-assembled peptide nanonets. Science. 2012;337:477-81 pubmed publisher
  6. Thaunat O, Granja A, Barral P, Filby A, Montaner B, Collinson L, et al. Asymmetric segregation of polarized antigen on B cell division shapes presentation capacity. Science. 2012;335:475-9 pubmed publisher
  7. Kane M, Case L, Kopaskie K, Kozlova A, MacDearmid C, Chervonsky A, et al. Successful transmission of a retrovirus depends on the commensal microbiota. Science. 2011;334:245-9 pubmed publisher
  8. Arnon T, Xu Y, Lo C, Pham T, An J, Coughlin S, et al. GRK2-dependent S1PR1 desensitization is required for lymphocytes to overcome their attraction to blood. Science. 2011;333:1898-903 pubmed publisher
  9. Rosas Ballina M, Olofsson P, Ochani M, Valdés Ferrer S, Levine Y, Reardon C, et al. Acetylcholine-synthesizing T cells relay neural signals in a vagus nerve circuit. Science. 2011;334:98-101 pubmed publisher
  10. Wild P, Farhan H, McEwan D, Wagner S, Rogov V, Brady N, et al. Phosphorylation of the autophagy receptor optineurin restricts Salmonella growth. Science. 2011;333:228-33 pubmed publisher
  11. Bendall S, Simonds E, Qiu P, Amir E, Krutzik P, Finck R, et al. Single-cell mass cytometry of differential immune and drug responses across a human hematopoietic continuum. Science. 2011;332:687-96 pubmed publisher
  12. Corse E, Gottschalk R, Krogsgaard M, Allison J. Attenuated T cell responses to a high-potency ligand in vivo. PLoS Biol. 2010;8: pubmed publisher
  13. Sasai M, Linehan M, Iwasaki A. Bifurcation of Toll-like receptor 9 signaling by adaptor protein 3. Science. 2010;329:1530-4 pubmed publisher
  14. Klatt N, Harris L, Vinton C, Sung H, Briant J, Tabb B, et al. Compromised gastrointestinal integrity in pigtail macaques is associated with increased microbial translocation, immune activation, and IL-17 production in the absence of SIV infection. Mucosal Immunol. 2010;3:387-98 pubmed publisher
  15. Shembade N, Ma A, Harhaj E. Inhibition of NF-kappaB signaling by A20 through disruption of ubiquitin enzyme complexes. Science. 2010;327:1135-9 pubmed publisher
  16. Jakus Z, Simon E, Frommhold D, Sperandio M, Mócsai A. Critical role of phospholipase Cgamma2 in integrin and Fc receptor-mediated neutrophil functions and the effector phase of autoimmune arthritis. J Exp Med. 2009;206:577-93 pubmed publisher
  17. Kobayashi T, Kim T, Jacob A, Walsh M, Kadono Y, Fuentes Pananá E, et al. TRAF6 is required for generation of the B-1a B cell compartment as well as T cell-dependent and -independent humoral immune responses. PLoS ONE. 2009;4:e4736 pubmed publisher
  18. Joo Y, Karrasch T, Muhlbauer M, Allard B, Narula A, Herfarth H, et al. Tomato lycopene extract prevents lipopolysaccharide-induced NF-kappaB signaling but worsens dextran sulfate sodium-induced colitis in NF-kappaBEGFP mice. PLoS ONE. 2009;4:e4562 pubmed publisher
  19. Nold Petry C, Nold M, Zepp J, Kim S, Voelkel N, Dinarello C. IL-32-dependent effects of IL-1beta on endothelial cell functions. Proc Natl Acad Sci U S A. 2009;106:3883-8 pubmed publisher
  20. Maynard C, Hatton R, Helms W, Oliver J, Stephensen C, Weaver C. Contrasting roles for all-trans retinoic acid in TGF-beta-mediated induction of Foxp3 and Il10 genes in developing regulatory T cells. J Exp Med. 2009;206:343-57 pubmed publisher
  21. Hou W, Kang H, Kim B. Th17 cells enhance viral persistence and inhibit T cell cytotoxicity in a model of chronic virus infection. J Exp Med. 2009;206:313-28 pubmed publisher
  22. Schenten D, Kracker S, Esposito G, Franco S, Klein U, Murphy M, et al. Pol zeta ablation in B cells impairs the germinal center reaction, class switch recombination, DNA break repair, and genome stability. J Exp Med. 2009;206:477-90 pubmed publisher
  23. Scatizzi J, Mavers M, Hutcheson J, Young B, Shi B, Pope R, et al. The CDK domain of p21 is a suppressor of IL-1beta-mediated inflammation in activated macrophages. Eur J Immunol. 2009;39:820-5 pubmed publisher
  24. Imaeda A, Watanabe A, Sohail M, Mahmood S, Mohamadnejad M, Sutterwala F, et al. Acetaminophen-induced hepatotoxicity in mice is dependent on Tlr9 and the Nalp3 inflammasome. J Clin Invest. 2009;119:305-14 pubmed publisher
  25. Dienz O, Eaton S, Bond J, Neveu W, Moquin D, Noubade R, et al. The induction of antibody production by IL-6 is indirectly mediated by IL-21 produced by CD4+ T cells. J Exp Med. 2009;206:69-78 pubmed publisher
  26. Yang X, Banerjee Y, Fernandez J, Deguchi H, Xu X, Mosnier L, et al. Activated protein C ligation of ApoER2 (LRP8) causes Dab1-dependent signaling in U937 cells. Proc Natl Acad Sci U S A. 2009;106:274-9 pubmed publisher
  27. Kuula H, Salo T, Pirilä E, Tuomainen A, Jauhiainen M, Uitto V, et al. Local and systemic responses in matrix metalloproteinase 8-deficient mice during Porphyromonas gingivalis-induced periodontitis. Infect Immun. 2009;77:850-9 pubmed publisher
  28. Ahn S, Byun K, Cho K, Kim J, Yoo J, Kim D, et al. Human microglial cells synthesize albumin in brain. PLoS ONE. 2008;3:e2829 pubmed publisher
  29. Lin M, Jackson P, Tester A, Diaconu E, Overall C, Blalock J, et al. Matrix metalloproteinase-8 facilitates neutrophil migration through the corneal stromal matrix by collagen degradation and production of the chemotactic peptide Pro-Gly-Pro. Am J Pathol. 2008;173:144-53 pubmed publisher
  30. Schneider D, Manzan M, Crawford R, Chen W, Kaminski N. 2,3,7,8-Tetrachlorodibenzo-p-dioxin-mediated impairment of B cell differentiation involves dysregulation of paired box 5 (Pax5) isoform, Pax5a. J Pharmacol Exp Ther. 2008;326:463-74 pubmed publisher
  31. Mortier E, Woo T, Advincula R, Gozalo S, Ma A. IL-15Ralpha chaperones IL-15 to stable dendritic cell membrane complexes that activate NK cells via trans presentation. J Exp Med. 2008;205:1213-25 pubmed publisher
  32. Mazurkiewicz P, Thomas J, Thompson J, Liu M, Arbibe L, Sansonetti P, et al. SpvC is a Salmonella effector with phosphothreonine lyase activity on host mitogen-activated protein kinases. Mol Microbiol. 2008;67:1371-83 pubmed publisher
  33. Wu W, Alexis N, Chen X, Bromberg P, Peden D. Involvement of mitogen-activated protein kinases and NFkappaB in LPS-induced CD40 expression on human monocytic cells. Toxicol Appl Pharmacol. 2008;228:135-43 pubmed publisher