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.

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4918 total record number 290 records this year

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4918 citations found

Tolerogenic nanovaccine for prevention and treatment of autoimmune encephalomyelitis

Park, J;Le, QV;Wu, Y;Lee, J;Oh, YK;

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

Postnatal deletion of Spns2 prevents neuroinflammation without compromising blood vascular functions

Hasan, Z;Nguyen, TQ;Lam, BWS;Wong, JHX;Wong, CCY;Tan, CKH;Yu, J;Thiam, CH;Zhang, Y;Angeli, V;Nguyen, LN;

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

ORAI3 is dispensable for store-operated Ca2+ entry and immune responses by lymphocytes and macrophages

Wang, L;Noyer, L;Wang, YH;Tao, AY;Li, W;Zhu, J;Saavedra, P;Hoda, ST;Yang, J;Feske, S;

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

Imaging Inflammasome Activation in Microglia

Martin, NP;Harry, GJ;

Product: LPS from Escherichia coli O111:B4

GAB functions as a bioenergetic and signalling gatekeeper to control T cell inflammation

Kang, S;Liu, L;Wang, T;Cannon, M;Lin, P;Fan, TW;Scott, DA;Wu, HJ;Lane, AN;Wang, R;

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

MW‑9, a chalcones derivative bearing heterocyclic moieties, attenuates experimental autoimmune encephalomyelitis via suppressing pathogenic TH17 cells

Liu, B;Mao, Z;Yin, N;Gu, Q;Gu, Q;Qi, Y;Li, X;Yang, H;Wu, Z;Zou, N;Ying, S;Wan, C;

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

Combined IgE neutralization and Bifidobacterium longum supplementation reduces the allergic response in models of food allergy

An, SB;Yang, BG;Jang, G;Kim, DY;Kim, J;Oh, SM;Oh, N;Lee, S;Moon, JY;Kim, JA;Kim, JH;Song, YJ;Hyun, HW;Kim, J;Lee, K;Lee, D;Kwak, MJ;Kim, BK;Park, YK;Hong, CP;Kim, JH;Lim, HS;Ryu, MS;Jin, HT;Lee, SW;Chang, YS;Park, HS;Sung, YC;Jang, MH;

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

  • Food allergy model

    … For the peanut-induced systemic anaphylaxis model50, C3H/HeJ mice were intragastrically sensitized with 10 mg peanut extract (GREER Laboratories, USA) and 20 μg cholera toxin (List Biological Laboratories, USA) 4 times weekly. The animals were then orally boosted with 50 mg peanut extract and 20 μg cholera toxin twice every 2 weeks. At week 8,200 mg peanut extract was orally administered and rectal temperature was measured. In this model, IgETRAP was intraperitoneally injected the day before challenge of 200 mg peanut, and 5 × 109 cfu of B. longum was intragastrically administered to each mouse (5 × 109 cfu head−1) every day from week 5 to 8. …

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

Protocol to utilize fresh uncultured human lung tumor cells for personalized functional diagnostics

Talwelkar, SS;Lähdeniemi, IAK;Mäyränpää, MI;Hemmes, A;Linnavirta, N;Räsänen, J;Knuuttila, A;Wennerberg, K;Verschuren, EW;

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

E3 ubiquitin ligase NEDD4L negatively regulates inflammation by promoting ubiquitination of MEKK2

Li, H;Wang, N;Jiang, Y;Wang, H;Xin, Z;An, H;Pan, H;Ma, W;Zhang, T;Wang, X;Lin, W;

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

Product: Anti-Cholera Toxin B Subunit (Goat)

  • 2.4. Immunohistochemistry

    Following transcardial perfusion, the brains were dissected and postfixed in 4% PFA for 1.5 h at room temperature (RT). Subsequently, the brains were transferred to 10% sucrose in 0.1 M PB and left overnight at 4 °C, before being embedded in gelatin. The brains were incubated in 12% gelatin/10% sucrose in 0.1 M PB for 30 min at 37 °C, embedded in a plastic mold and left at 4 °C for at least 30 min to harden. They were then cut in small blocks and placed in a 10% formalin/30% sucrose in 0.1 M PB for at least 2.5 h at RT. Embedded brains were transferred to 30% sucrose in 0.1 M PB overnight at 4 °C before being sliced on a Leica SM2000R microtome (Leica Biosystems, Nussloch, Germany) at 50 µm. To prepare the slices for antibody staining, they were blocked for one hour with 10% normal horse serum (NHS) and 0.5% triton in PBS at RT after rinsing in PBS. Subsequently, slices were stained for goat anti-CTB (703; 1:15,000, List Biological Laboratories, Inc., Campbell, NJ, USA) in 2% NHS and 0.4% triton in PBS, and left 24 h at RT. The CTB antibody turned out to be specific enough for unambiguous identification of intensely labeled CTB+ cells on 10× versus background (intrinsic) fluorescence (for which controls have been previously described by our lab [31]). …

    Product #703 – Anti-Cholera Toxin B Subunit (Goat)