Citations

Bacterial Toxin Research Citations

We’ve gathered published citations for the past many years so that researchers can easily review at their convenience from among the thousands of published articles, how they might use our products in detail or apply these ideas to their own novel thinking for new research.

Search through, read and share our information rich citations below!

Contact us with any questions.

4973 total record number 1 records this year

To narrow your search, use one or more of the following search menus below.

To search by keyword, you may search by the cell/animal/assay/protein/research or publication
Page 90 out of 498
4973 citations found

Immunological Evidence of Variation in Exposure and Immune Response to Bacillus anthracis in Herbivores of Kruger and Etosha National Parks

Ochai, SO;Crafford, JE;Hassim, A;Byaruhanga, C;Huang, YH;Hartmann, A;Dekker, EH;van Schalkwyk, OL;Kamath, PL;Turner, WC;van Heerden, H;

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

  • Anti-Protective Antigen (PA) Enzyme-Linked Immunosorbent Assay

    In this study, serum samples were assessed for the presence of specific antibodies against the anthrax PA as described by Yu et al. (56), and Ndumnego et al. (23). Briefly, microtiter plates (Thermo Scientific™ Pierce 96-well Plates-Corner, USA) were coated overnight with 0.5 μg/ml rPA (List Biological Laboratories Inc., USA) in bicarbonate buffer at 4°C. …

    Product #171E – Anthrax Protective Antigen (PA), Recombinant from B. anthracis

Amoxicillin does not affect the development of cow’s milk allergy in a Brown Norway rat model

Locke, AV;Larsen, JM;Graversen, KB;Licht, TR;Bahl, MI;Bøgh, KL;

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

  • 2.2 Animal experiment

    Female BN rats with an age of 3.5-5 weeks were allocated into four groups of 12 rats (Figure 1) for the induction of CMA using a CT-mediated model.27 Half of the rats were gavaged daily with 30 mg of amoxicillin (AMX) in 0.5 mL sterile Milli Q water and the other half with 0.5 mL sterile Milli Q water alone (CTR) for a total of 6 weeks. Starting on Day 7, the oral gavage solutions additionally included 10 mg WPC without (CTR and AMX) or with (CTR+CT and AMX+CT) 20 μg of CT three times per week for 5 weeks. The dose and duration of AMX administration were based on our previous studies in BN rats.25, 28 In order to include rats with a uniform age, the experiment was divided into two separate sets of experiments without (CTR and AMX groups) and with (CTR+CT and AMX+CT groups) CT respectively.

    … while CT was purchased from List Biological Laboratories Inc (cat. no. 100B, Cambell, CA, US). …

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

PD-1 agonism by anti-CD80 inhibits T cell activation and alleviates autoimmunity

Sugiura, D;Okazaki, IM;Maeda, TK;Maruhashi, T;Shimizu, K;Arakaki, R;Takemoto, T;Ishimaru, N;Okazaki, T;

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

The C-type lectin receptor Clec1A plays an important role in the development of experimental autoimmune encephalomyelitis by enhancing antigen presenting ability of dendritic cells and inducing inflammatory cytokine IL-17

Makusheva, Y;Chung, SH;Akitsu, A;Maeda, N;Maruhashi, T;Ye, XQ;Kaifu, T;Saijo, S;Sun, H;Han, W;Tang, C;Iwakura, Y;

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

Control of water intake by a pathway from the nucleus of the solitary tract to the paraventricular hypothalamic nucleus

Volcko, KL;Brakey, DJ;McNamara, TE;Meyer, MJ;McKay, NJ;Santollo, J;Daniels, D;

Product: Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt

Transplanting Neural Progenitor Cells into a Chronic Dorsal Column Lesion Model

Hayakawa, K;Jin, Y;Bouyer, J;Connors, TM;Otsuka, T;Fischer, I;

Product: Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt

  • 2.4. Cholera Toxin Subunit B (CTB) Labeling

    To trace sensory axon regeneration, CTB was used to label the dorsal column axons. Three days before the end of experiment, animals were anesthetized with isoflurane at 4–5% (v/v) for induction and 2–3% (v/v) for maintenance, respectively. Sciatic nerves of both hindlimbs were exposed and CTB (2 μL, 1% in distilled water, List Biological Laboratories, Campbell, CA, USA) was injected into the sciatic nerve using a 10 µL Hamilton syringe with a 33-gauge needle. The incision was then closed. Animal care was performed as stated previously.

    Product #104 – Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt

The volume-regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling

Concepcion, AR;Wagner, LE;Zhu, J;Tao, AY;Yang, J;Khodadadi-Jamayran, A;Wang, YH;Liu, M;Rose, RE;Jones, DR;Coetzee, WA;Yule, DI;Feske, S;

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

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

  • 2.3. Chick Normal Small Intestinal Epithelial Cells Culture and Treatment

    … In addition, to explore the intracellular signaling pathway activated by butyrate, we added 10 μM LY294002 (an inhibitor of PI3k, MCE, Weehawken, NJ, USA), 2 μM GSK690693 (an inhibitor of AKT, MCE, Weehawken, NJ, USA), 5 μM CHIR99021 (an inhibitor of GSK-3β, MCE, Weehawken, NJ, USA), 20 μM 4-CMTB (an agonist of GPR43, MCE, Weehawken, NJ, USA), 5 μM AR420626 (an agonist of GPR41, GlpBio, Montclair, NJ, USA), 50 ng/mL PTX (an inhibitor of Gi, List Biological Laboratories, Campbell, CA, USA) and 10 μM Ym254890 (an inhibitor of Gq, Wako Pure Chemical Industries, Ltd. Osaka, Japan), respectively, into CIECs for 0.5 h before the addition of exogenous butyrate (0.5 mM, Sigma-Aldrich, St. Louis, MO, USA). Twenty-four hours later, CIECs were collected for western blot assay. Each assay used a repeat of six wells.

    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)

Healthy Properties of a New Formulation of Pomegranate-Peel Extract in Mice Suffering from Experimental Autoimmune Encephalomyelitis

Vallarino, G;Salis, A;Lucarini, E;Turrini, F;Olivero, G;Roggeri, A;Damonte, G;Boggia, R;Di Cesare Mannelli, L;Ghelardini, C;Pittaluga, A;

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

  • 4.7. Animals and EAE Induction

    Mice (female, strain C57BL/6J, seven weeks old) were obtained from Charles River (Calco, Italy) and housed at the animal facility of the Department of Pharmacy, Section of Pharmacology and Toxicology, School of Medical and Pharmaceutical Sciences, University of Genoa (authorization n. 484 of 2004, June 8th). EAE was induced in mice as previously described [45]. Briefly, mice were injected subcutaneously with incomplete Freund’s adjuvant containing 200 μg myelin oligodendrocyte protein 35–55 (MOG35–55; Espikem S.r.l, Prato, Italy) peptide and 8 mg/ml Mycobacterium tuberculosis (strain H37Ra; Becton, Dickinson and Company, Franklin Lakes, NJ, USA), followed by intraperitoneal administration of 400 ng of Pertussis toxin (List Biological Laboratories, Campbell, CA, USA) on day 0 and after 48 h. …

    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)

A Distinct Hibiscus sabdariffa Extract Prevents Iron Neurotoxicity, a Driver of Multiple Sclerosis Pathology

Mishra, MK;Wang, J;Mirzaei, R;Chan, R;Melo, H;Zhang, P;Ling, CC;Bruccoleri, A;Tang, L;Yong, VW;

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

  • 2.8. EAE and Spinal Cord Histology

    All experiments were conducted with ethics approval from the Animal Care Committee at the University of Calgary under guidelines of the Canadian Council of Animal Care. Eight-to-ten-week-old C57BL/6 female mice (Charles River Laboratories, Montreal, QC, Canada) with an average weight of 22 g were immunized subcutaneously with 50 μg/100 μL of myelin oligodendrocyte glycoprotein (MOG) 35–55 peptide (Protein and Nucleic acid facility, Stanford University, USA) in CFA supplemented with 4 mg/mL heat-inactivated Mycobacterium tuberculosis H37Ra (Sigma). This method has been previously described [21,47]. A 50 μL emulsion was deposited on either side of the tail base. Pertussis toxin (PTX) (300 ng/200 μL, List Biological Laboratories, Campbell, CA, USA) was injected intraperitoneally on days 0 and 2 after MOG immunization.

    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)