Citations

Bacterial Toxin Research Citations

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4918 citations found

Product: LPS from Escherichia coli O55:B5

  • 2.2. Cell culture
    The HDFa cell line was bought from the American Type Culture Collection (ATCC; Minnesota, USAHB-8065). It was cultured in Park Memorial Institute (RPMI -1640) culture media with glutamine 2 mM (bio west, Nampa, cat n L0498-500), 10% fetal bovine serum (PAA, Pasching Austria, cat. no. A11-151) and penicillin with streptomycin 1% (Lonza, Verviers, Belgium, cat. no. DE17-602E). The HDFa cells were grown in 50 cm2 flask (Greinerbio-one GmbH Maybachstr.272636 Frickenhausen, Germany) and preserved in typical humidified incubator supplied with 5% CO2, 95% air at 37 °C (New Brunswick Scientific- Innova co-170). Cells were washed with cold phosphate buffered saline, trypsinized, harvested and centrifuged to form cell pellets. The cultured HDFa were divided into four groups as follows:

    Group I (Control): The HDFa cells received no treatment.

    Group II (LPS): The HDFa cells were stimulated with LPS (10 ng/mL, Escherichia coli 055:B5, List Biological Laboratories, CA, USA) for 48 h (Skioldebrand et al., 2018).

    Product #203A – LPS from Escherichia coli O55:B5

Nephronectin influences EAE development by regulating the Th17/Treg balance via reactive oxygen species

Honda, M;Segawa, T;Ishikawa, K;Maeda, M;Saito, Y;Kon, S;

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

Immune-mediated neurodegenerative trait provoked by multimodal derepression of long-interspersed nuclear element-1

Takahashi, F;Zhang, C;Hohjoh, H;Raveney, B;Yamamura, T;Hayashi, N;Oki, S;

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

  • STAR★Methods
    Key resources table

    Pertussis toxin List Biological Laboratories Cat#180

    Mice, EAE induction and scoring
    For EAE experiments, 6–8 weeks old mice were used. mSOD1 and 5xFAD mice were maintained up to 150 days and 15 months after birth, respectively. …

    Mice, aged 6-9 weeks, were immunized subcutaneously with 100 μg MOG35-55 peptide (synthesized by Toray Research Center, Japan) emulsified in complete Freund’s adjuvant containing 1 mg heat-killed Mycobacterium tuberculosis H37RA (Difco). The mice were injected intraperitoneally (i.p.) with 100 ng of pertussis toxin (List Biological Laboratories, USA) at the time of immunization and 2 days later. …

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

Patients with HIV-associated cancers have evidence of increased T cell dysfunction and exhaustion prior to cancer diagnosis

Chaudhary, O;Trotta, D;Wang, K;Wang, X;Chu, X;Bradley, C;Okulicz, J;Maves, RC;Kronmann, K;Schofield, CM;Blaylock, JM;Deng, Y;Schalper, KA;Kaech, SM;Agan, B;Ganesan, A;Emu, B;

Product: Enterotoxin Type B from Staphylococcus aureus

  • … PBMCs were washed and stimulated with 1 µg/ mL Staphylococcus endotoxin B (SEB; List Biological Laboratories, California, USA) in the presence of Brefeldin A (Thermo Fisher Scientific, Massachusetts, USA) at 37°C and 5% CO2 for 16 hours …

Parental uveitis causes elevated hair loss in offspring of C57BL/6J mice

Liu, J;Yin, G;Hu, K;Huang, H;Xu, F;Yang, Y;Chen, F;

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

Edaravone attenuates disease severity of experimental auto-immune encephalomyelitis and increases gene expression of Nrf2 and HO-1

Michali?ková, D;Kübra Öztürk, H;Hroudová, J;?upták, M;Ku?era, T;Hrn?í?, T;Kutinová Canová, N;Šíma, M;Slana?, O;

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

  • Animals and induction of EAE

    The EAE was actively induced in conventional inbred female C57Bl/6J mice (9-13 weeks old)
    by immunization with myelin oligodendrocyte glycoprotein (MOG) 35-55 peptide (Prospec,
    Rehovot, Israel) and complete Freund’s adjuvant (CFA) containing Mycobacterium
    tuberculosis H37Ra (Sigma-Aldrich, Prague, Czech Republic). The MOG/CFA emulsion was
    prepared by connecting two glass syringes to a 3-way connector and passing the solutions
    through the connector. The emulsion was injected subcutaneously in two 50 μl doses. In total,
    100 μg of MOG peptide per mouse was administered. To facilitate the transfer of lymphocytes
    into the CNS, 300 ng of pertussis toxin (List Biologicals, Campbell, California, USA) in 200
    μl of phosphate buffer saline (PBS) was injected intraperitoneally two hours and two days after
    the EAE induction [14].

    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)

Biased agonists of the chemokine receptor CXCR3 differentially signal through G?i:?-arrestin complexes

Zheng, K;Smith, JS;Eiger, DS;Warman, A;Choi, I;Honeycutt, CC;Boldizsar, N;Gundry, JN;Pack, TF;Inoue, A;Caron, MG;Rajagopal, S;

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

The innate immune receptor Nlrp12 suppresses autoimmunity to the retina

Lee, EJ;Napier, RJ;Vance, EE;Lashley, SJ;Truax, AD;Ting, JP;Rosenzweig, HL;

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

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

A Potent Inhibitor of the Cystic Fibrosis Transmembrane Conductance Regulator Blocks Disease and Morbidity Due to Toxigenic Vibrio cholerae

Rivera-Chávez, F;Meader, BT;Akosman, S;Koprivica, V;Mekalanos, JJ;

Product: Cholera Toxin (AZIDE-FREE) from Vibrio cholerae

  • … To test whether (R)-BPO-27 treatment reduces CT-dependent diarrheal disease symptoms, groups of 3–5-day-old wild type (CD-1) mice were mock treated with the vehicle control containing DMSO in Luria broth (LB), purified CT (List Biological Laboratories, Campbell, CA, USA), purified CT mixed with (R)-BPO-27, or with (R)-BPO-27 alone (Figure 1A). A second dose of vehicle or (R)-BPO-27 was administered 6 h after the initial challenge. Mice treated with CT alone had statistically significant elevated FA ratios (diarrheal disease) at 22 h (Figure 1B). By contrast, mice treated with CT mixed with (R)-BPO-27 developed significantly less diarrheal disease than mice treated with CT alone (Figure 1B). Importantly, there was no significant difference in diarrheal disease between mice treated with CT and (R)-BPO-27 and mice treated with (R)-BPO-27 alone or with the vehicle control. We conclude that two doses of (R)-BPO-27 protect neonatal mice from diarrheal disease induced by oral-gastric administration of CT. These results are consistent with the findings of Verkman and colleagues who studied the ability of (R)-BPO-27 to block fluid accumulation induced by CT and STa in isolated (i.e., ligated) intestinal segments of adult mice [23]. …

    Product #100B – Cholera Toxin (AZIDE-FREE) from Vibrio cholerae