Citations

Bacterial Toxin Research Citations

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4918 citations found

Product: Pertussis Toxin from B. pertussis (in Glycerol)

  • 193 at concentrations of 0.1, 1, and 5 ?M in a fresh medium was added to the cells. All reactions, including controls without the inhibitors, contained 0.05% DMSO. After 30 minutes of incubation at 37°C under normal cell culturing conditions, pertussis holotoxin (List Biological Laboratories Inc., 179A) was added to the cells at concentrations of 10 or 100 ng/ml. Cells were then incubated for an additional 2 hours, placed on ice,

Product: LIPID A monophosphoryl from Salmonella minnesota R595

  • Labelling of Lipid A. One mg of commercially obtained lipid A (List Laboratories, Campbell, CA) or lipid A derived from Escherichia coli K 235 LPS by the method described by Galanos et al

Product: LIPID A monophosphoryl from Salmonella minnesota R595

  • 401 from List Labs). LPS was directly diluted and aliquoted to 100 ?g/ml stock solutions in UP water. MPLA was first diluted in 10% DMSO and then aliquoted to 100 ?g/ml

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

  • sis toxin was administered on days 0 and 2 (100 ng/mouse, i.p) (List Biological Laboratories, Campbell, CA, USA). Sera were collected on day 0 and day 21 post-immunization at termination

Product: Anthrax Lethal Factor (LF), Recombinant from B. anthracis

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

  • 2.1.2 Study II: Examination of the contribution of neuroinflammatory processes such as
    BBB leakage and focal inflammation to changes in mechanical properties

    For in vivo MRE and MRI experiments adoptive transfer EAE was induced in 21 SJL mice (female, 9-12 weeks, Janvier, SAS, France, registration number G106/19) by the transfer of myelin proteolipid protein (PLP)-reactive lymphocytes. SJL mice were used as the animal strain of choice to induce EAE (active and adoptive transfer), as they display a high disease susceptibility after induction. PLP-reactive lymphocytes were obtained from 22 donor mice, which were actively immunized as previously described (31, 34) using 200 mg of the myelin peptide PLP139-151 emulsified with 200 ml complete Freund´s adjuvant (Thermo Fischer Scientific, United States) and 800 mg Mycobacterium tuberculosis
    H37Ra (Difico, United States). As described in (31), on days 0 and 2 postimmunization (p.i.), 250 ng pertussis toxin (List Biological Laboratories, United States) was injected intraperitoneally. Donor animals were sacrificed on day 10 p.i., axillary and inguinal lymph nodes were collected and cells cultured as described (35). Cells were harvested after 4 days in culture with RPMI 1640 medium (supplemented with 2 mM L-glutamine, 100 units/ml penicillin, 100 mg/ml streptomycin and 10 % fetal bovine serum) (Gibco, Thermo Fischer Scientific) containing 12.5 mg/ml PLP. Into each of the 21 recipient mice 30 million cells were intraperitoneally injected. …

    Author did not specify which List Labs Pertussis Toxin was utilized. List Labs provides the following Pertussis Toxin products:
    Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer
    Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)
    Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

  • 2.2.1 Active EAE

    For Studies I, II and III active EAE was induced in SJL mice. Therefore, 9 – 12-week-old mice (Janvier, SAS, France) were subcutaneously immunized with an emulsion containing 250 µg of a PLP139-151, 800 µg M. tuberculosis H37Ra (Difco, USA) and 100 µl of complete Freund’s adjuvant (CFA; Thermo Fisher Scientific, USA) in addition to an intraperitoneal injection of 250 ng pertussis toxin (List Biological Laboratories, USA) on the same day and 2 days later. …

    Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Luminespib inhibitor

OHTA, H;SATO, K;MURATA, N;DAMIRIN, A;MALCHINKHUU, E;KON, J;KIMURA, T;TOBO, M;YAMAZAKI, Y;WATANABE, T;YAGI, M;SATO, M;SUZUKI, R;MUROOKA, H;SAKAI, T;NISHITOBA, T;IM, D;NOCHI, H;TAMOTO, K;TOMURA, H;OKAJIMA, F;

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

The antioxidant N-acetyl cysteine inhibits cytokine and prostaglandin release in human fetal membranes stimulated ex vivo with lipoteichoic acid or live group B streptococcus

Park, HR;Harris, SM;Boldenow, E;Aronoff, DM;Rea, M;Xi, C;Loch-Caruso, R;

Product: LPS from Salmonella typhimurium

Exposure to Mycobacterium remodels alveolar macrophages and the early innate response to Mycobacterium tuberculosis infection

Mai, D;Jahn, A;Murray, T;Morikubo, M;Lim, PN;Cervantes, MM;Pham, LK;Nemeth, J;Urdahl, K;Diercks, AH;Aderem, A;Rothchild, AC;

Product: LPS from Salmonella minnesota R595 (Re)

  • Alveolar macrophage Ex Vivo stimulation

    AMs were isolated by bronchoalveolar lavage and pooled from 5 mice per group. Cells were plated at a density of 5 x 104 cells/well (96-well plate) in complete RPMI (RPMI plus FBS (10%, VWR), L-glutamine (2mM, Invitrogen), and Penicillin-Streptomycin (100 U/ml; Invitrogen) and allowed to adhere overnight in a 37°C humidified incubator (5% CO2). Media with antibiotics and non-adherent cells were washed out prior to stimulation. AM were stimulated with LPS (LPS from Salmonella Minnesota, List Biologicals, #R595, 10 ng/ml), Pam3Cys (Pam3CSK4, EMC Microcollections, GmbH, 10 ng/ml), or H37Rv (effective MOI ~2:1). H37Rv was prepared by culturing from frozen stock in 7H9 media at 37°C for 48 hours to O.D. of 0.1–0.3. …

    Product #304 – LPS from Salmonella minnesota R595 (Re)