Citations

Bacterial Toxin Research Citations

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4917 total record number 289 records this year

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Page 195 out of 492
4917 citations found

MicroRNA-34a Promotes Endothelial Dysfunction and Mitochondrial-Mediated Apoptosis in Murine Models of Acute Lung Injury

Shah, D;Das, P;Alam, MA;Mahajan, N;Romero, F;Shahid, M;Singh, H;Bhandari, V;

Product: LPS from Escherichia coli O111:B4

Visualizing the Contribution of Keratin-14+ Limbal Epithelial Precursors in Corneal Wound Healing

Park, M;Richardson, A;Pandzic, E;Lobo, EP;Whan, R;Watson, SL;Lyons, JG;Wakefield, D;Di Girolamo, N;

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

  • Monitoring Corneal Wound Resolution in Organ Culture:

    Confetti mice were wounded as described above. The animals were euthanized and their eyes immediately enucleated. Paired (wounded and intact) globes were embedded in sterile 1.5% agarose and placed within the microscope’s imaging/incubation chamber, set to 37C and 5% CO2 prior to immersion in defined keratinocyte serum-free medium (Gibco, Fremont, CA) containing 50 nM recombinant human epidermal growth factor (Peprotech, Rocky Hill, NJ), 500 nM cholera toxin (List Biological Labs, Campbell, CA) and 100 U/mL penicillin-streptomycin (Gibco). Eyes were imaged every 2 hr over 48 hr by light-sheet microscopy (Zeiss Lightsheet Z.1) using a 5/0.16 detection lens and 5/0.1 illumination lens as described above.

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

Chemically modified peanut extract shows increased safety while maintaining immunogenicity

van der Kleij, HPM;Warmenhoven, HJM;van Ree, R;Versteeg, SA;Pieters, RHH;Dreskin, SC;Knulst, AC;Hoffen, EV;Opstelten, DJE;Koppelman, SJ;Smit, JJ;

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

Product: Anti-Botulinum Neurotoxin, Type A (Mouse lgG monoclonal F1-40), Frozen Liquid

A comparison of biological activity of commercially available purified native botulinum neurotoxin serotypes A1 to F1 invitro, exvivo, and invivo

Donald, S;Elliott, M;Gray, B;Hornby, F;Lewandowska, A;Marlin, S;Favre-Guilmard, C;Prier, C;Cornet, S;Kalinichev, M;Krupp, J;Fonfria, E;

Product: Botulinum Neurotoxin Type B Complex, Nicked, from Clostridium botulinum

  • Botulinum toxins (BoNTs) and general reagents:

    …  Serotypes A, B, and E were also purchased from List Biological Laboratories as complex toxins and BSA was added during the reconstitution step of the lyophilized powder supplied, as recommended by the manufacturer. …

Product: Anti-Cholera Toxin B Subunit (Goat)

  • Table1

    Table showing primary and secondary antibodies:

    Goat anti-CtB, List Laboratories 703, …

    Immunouorescencestaining:

    Tissues were obtained from a previous study [1].  We evaluated with immunolabeling (Table1) whether neurotrophin-3 treatment regulates Sema4C expression specically in TrkC+ afferent neurons, which include proprioceptive afferents. …

Pharmacological profile of the neuropeptide S receptor: Dynamic mass redistribution studies

Ruzza, C;Ferrari, F;Guerrini, R;Marzola, E;Preti, D;Reinscheid, RK;Calo, G;

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

Enhanced sensitivity to cholera toxin in female ADP-ribosylarginine hydrolase (ARH1)-deficient mice

Watanabe, K;Kato, J;Zhu, J;Oda, H;Ishiwata-Endo, H;Moss, J;

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

  • Materials:

    Cholera toxin was purchased from List Biological Laboratory, Inc, California, USA; …

    Induction of fluid accumulation by cholera toxin (CT):

    Fluid accumulation in mouse intestinal loops in response to CT was performed in ARH1+/+ and ARH1-/- mice [28, 39]. After mice were anesthetized, intestine was exteriorized through a midline incision. Two or three intestinal segments of about 4 cm length each were generated by ligation with nylon suture, and 0.2 ml of PBS or PBS containing either 0.5 µg CT or 5 mM 8-Bromo-cAMP were injected into each loop [28]. …

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

Product: Alpha Toxin from C. septicum, Liquid

  • Indirect immunofluorescence analysis (IFA):

    …To resolve the C-terminal topology of TgATPaseP-GC, fresh extracellular parasites were stained with rabbit -HA (1:3000) and mouse -TgSag1 (1:10000) or rabbit -TgGap45 (1:8000) and -TgSag1 (1:10000) antibody combinations before and after permeabilization as described elsewhere (Blume et al. 2009). Briefly, 5 x 104 tachyzoites were released on BSA-coated coverslips and fixed with 4% PFA including 0.05% glutaraldehyde. Permeabilized coverslips were subjected to immunofluorescence assay as indicated above; however, all solutions were substituted to PBS for non-permeabilized staining as principle of the assay as shown in Figure 2B. To find the exact localization of TgATPaseP-GC protein, the IMC was separated from the PM by treating extracellular parasites with -toxin from Clostridium septicum (20 nM, 2 h) (List Biological Laboratories, US) followed by fixation on BSAcoated coverslips. In both cases, the standard secondary antibody staining procedure was performed afterwards, as described for immunofluorescence assay …

Increasing FIM2/3 antigen-content improves efficacy of Bordetella pertussis vaccines in mice in vivo without altering vaccine-induced human reactogenicity biomarkers in vitro

Queenan, AM;Dowling, DJ;Cheng, WK;Fa, K;Fernandez, J;Flynn, PJ;Joshi, S;Brightman, SE;Ramirez, J;Serroyen, J;Wiertsema, S;Fortanier, A;van den Dobbelsteen, G;Levy, O;Poolman, J;

Product: Fimbriae 2/3 from B. pertussis

  • Human blood sample processing and in vitro stimulation:

    … Human blood was anti-coagulated with 20 units/ml pyrogen-free sodium heparin (American Pharmaceutical Partners, Inc.; Schaumberg, IL). All blood products were kept at room temperature and processed within 4h from collection. For human whole blood assays, neonatal cord blood or adult whole blood (WB) was first diluted with sterile RPMI 1640 medium (Invitrogen; Carlsbad, CA) and 175l of the diluted WB was added to each well of a 96 well U-bottom plate (Becton Dickinson; Franklin Lakes, NJ, USA) containing 75l of RPMI, freshly prepared FIM proteins, or licensed vaccines at 10 the final concentration. The same formulations were used for both in vivo and in vitro assessment, so the FIM2/3 formulation was prepared by mixing dilutions of purified FIM2/3 (200g/ml, List Biological Laboratories, Inc.) in PBS, which at 1/10 human dose would correlate with 5g/250l. …’