Citations

Bacterial Toxin Research Citations

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4918 total record number 290 records this year

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Page 137 out of 492
4918 citations found

Leptin increases sympathetic nerve activity via induction of its own receptor in the paraventricular nucleus

Shi, Z;Pelletier, NE;Wong, J;Li, B;Sdrulla, AD;Madden, CJ;Marks, DL;Brooks, VL;

Product: Anti-Cholera Toxin B Subunit (Goat)

OnabotulinumtoxinA Displays Greater Biological Activity Compared to IncobotulinumtoxinA, Demonstrating Non-Interchangeability in Both In Vitro and In Vivo Assays

Rupp, D;Nicholson, G;Canty, D;Wang, J;Rhaume, C;Le, L;Steward, LE;Washburn, M;Jacky, BP;Broide, RS;Philipp-Dormston, WG;Brin, MF;Brideau-Andersen, A;

Product: SNAPtide® Peptide Substrate (o-Abz/Dnp) for C. botulinum Type A Neurotoxin

  • Light-Chain Activity High-Performance Liquid Chromatography (LCA-HPLC) Assay

    … Next, 25 μL of 200 μM SNAPtide 520 (List Biological Laboratories Inc., Campbell, CA, USA) was added to each reaction tube (equivalent to 13.3 μM SNAPtide 520) followed by incubation at 30 °C for 20 h (digestion step). Reactions were quenched following the addition of 25 μL of 5% trifluoroacetic acid (TFA). The contents of each tube were then transferred to HPLC vials for analysis. The fluorescently-labeled cleavage product(s) were separated and detected via a reverse-phase (RP)-HPLC method [28] using a Waters 2695 XE Separations Module and a Waters 2475 Multi λ Fluorescence Detector (Waters Corp., Milford, MA, USA). In brief, 25 µL of cleavage products were loaded onto a Symmetry C18 column (300 Å, 3.5 µm, 4.6 mm × 150 mm; Waters Corp.), maintained at 35 °C. Separation was accomplished using a 10−90% CH3CN (0.1% TFA) gradient for 30 min, with a flow-rate of 1 mL/min. The column effluent was monitored fluorescently (excitation λ = 322 nm, emission λ = 420 nm) to detect the o-aminobenzoic acid fluorophore on the N-terminal cleaved fragment of SNAPtide 520. SNAPtide cleavage product (#529, List Biological Laboratories, Inc.) was utilized to identify retention time of the cleavage product, as #529 is the unquenched calibration peptide for SNAPtide 520 substrate for C. botulinum type A neurotoxin.

    Product #520 – SNAPtide® Peptide Substrate (o-Abz/Dnp) for C. botulinum Type A Neurotoxin
    Product #529 – Unquenched Calibration Peptide for SNAPtide® 520 Substrate for C. botulinum Type A Neurotoxin

Stimulation with FITC-labeled antigens confers B cells with regulatory properties

Planchais, C;Rayes, J;Delignat, S;Pashova, S;Varthaman, A;Pashov, A;Bayry, J;Kaveri, SV;Dimitrov, JD;Lacroix-Desmazes, S;

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

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

Impaired Th17 immunity in recurrent C. difficile infection is ameliorated by fecal microbial transplantation

Cook, L;Rees, W;Wong, M;Wang, X;Peters, H;Oliveira, L;Lau, T;Mah, R;Bressler, B;Gomez, R;Chow, I;James, E;Kwok, W;Levings, M;Steiner, T;

Product: Toxin B Toxoid from Clostridium difficile

  • Reagents

    C. difficile TcdA and TcdB toxoids (formaldehyde inactivated; List Biological Laboratories Inc. Campbell, USA) were used at 10µg/mL and 5µg/mL respectively. …

Pharmacological inhibition of carnitine palmitoyl transferase 1 inhibits and reverses experimental autoimmune encephalitis in rodents

Mrkholt, AS;Oklinski, MK;Larsen, A;Bockermann, R;Issazadeh-Navikas, S;Nieland, JGK;Kwon, TH;Corthals, A;Nielsen, S;Nieland, JDV;

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

Loss of allergy-protective capacity of raw cow’s milk after heat treatment coincides with loss of immunologically active whey proteins

Abbring, S;Xiong, L;Diks, MAP;Baars, T;Garssen, J;Hettinga, K;van Esch, BCAM;

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

  • Experimental design animal study
    A schematic representation of the experimental timeline is depicted in Fig. 1B. Mice were orally exposed, by using a blunt needle, to 0.5 mL raw milk, the milk samples heated at 50 °C, 60 °C, 65 °C, 70 °C, 75 °C, 80 °C or PBS (as a control) for eight consecutive days (days-9 to -2). Subsequently, mice (n = 8 per group) were orally (by means of gavage) sensitized to 20 mg ovalbumin (OVA; 20 mg per 0.5 mL PBS; grade V; Sigma-Aldrich) using 15 μg cholera toxin (CT; List Biological Laboratories, Campbell, CA, USA) as an adjuvant (days 0, 7, 14, 21, and 28). …

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

BPTES inhibits anthrax lethal toxin-induced inflammatory response

Wang, J;Yang, D;Shen, X;Wang, J;Liu, X;Lin, J;Zhong, J;Zhao, Y;Qi, Z;

Product: Anthrax Protective Antigen (PA), Recombinant from B. anthracis

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

Aging imparts cell-autonomous dysfunction to regulatory T cells during recovery from influenza pneumonia

Morales-Nebreda, L;Helmin, K;Markov, N;Piseaux, R;Acosta, M;Abdala-Valencia, H;Politanska, Y;Singer, B;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Treg cell isolation and adoptive transfer

    Diphtheria toxin (List Biologicals, CA) was administered via intraperitoneal injection in 100µL of sterile PBS in the following doses and days relative to influenza A virus infection (day 0): 50 mcg/Kg on day -2 and 10 mcg/Kg every 48 hours starting on day 0 and ending on day 28 post-infection. Five days later, 1 x 106 young or aged splenic Treg cells in 100 µL of sterile PBS were transferred via retro-orbital injection into the
    influenza-treated Foxp3DTR mice.

    Product #150 – Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae