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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4945 citations found

Nicotine modulates the immunological function of dendritic cells through peroxisome proliferator-activated receptor- upregulation

Yanagita, M;Kobayashi, R;Kojima, Y;Mori, K;Murakami, S;

Product: LPS from Salmonella minnesota R595 (Re)

  • … Immature DCs with or without nicotine (NiDCs and MoDCs, respectively) were cultured with 10 ng/ml lipopolysaccharide (LPS; Salmonella minnesota; List Biological Laboratories, INC, Campbell, CA) to induce cytokine and chemokine production. …

Cellular cytoskeleton dynamics modulates non-viral gene delivery through RhoGTPases

Dhaliwal, A;Maldonado, M;Lin, C;Segura, T;

Product: Toxin B from Clostridium difficile

Vigorous response of human innate functioning IgM memory B cells upon infection by Neisseria gonorrhoeae.

So, NS;Ostrowski, MA;Gray-Owen, SD;

Product: Tetanus Toxoid from Clostridium tetani

  • ELISA:

    All ELISAs were read at 450 nm using a 1420 Victor3 (PerkinElmer) plate reader, unless otherwise indicated. Total Ig in cell culture supernatant was quantied by IgM, IgG, or IgA ELISA kits (Zeptometrix), used according to manufacturers instructions. To monitor Ag-specic Ig production, 96-well Maxisorp plates (Nunc) were coated with either heat-killed Opa2 gonococci (N302), keyhole limpet hemocyanin (KLH; Sigma-Aldrich), or tetanus toxoid (TT; List Biological Labs) resuspended in pH 7.4 PBS (Wisent). …

Caspase-1 has both proinflammatory and regulatory properties in Helicobacter infections, which are differentially mediated by its substrates IL-1 and IL-18

Hitzler, I;Sayi, A;Kohler, E;Engler, DB;Koch, KN;Hardt, WD;Mller, A;

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

Regulatory T cells selectively preserve immune privilege of self-antigens during viral central nervous system infection

Cervantes-Barragn, L;Firner, S;Bechmann, I;Waisman, A;Lahl, K;Sparwasser, T;Thiel, V;Ludewig, B;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Mice and Treg depletion:

    … To deplete Treg cells, DEREG mice were injected with DT (List Biological Laboratories). Mice were injected i.p. with 1 mg DT every other day over a period of 9 d starting with the rst injection 1 d prior MHVA59 infection. For adoptive transfer experiments, recipients were treated with DT on days 5, 7, and 9 postinfection (p.i.). Control mice (B6) received the same DT treatment as DEREG mice. 2D2 3 DEREG donor mice were injected with 1 mg DT 1 d prior to cell isolation.

Differential projections from the lateral habenula to the rostromedial tegmental nucleus and ventral tegmental area in the rat

Gonalves, L;Sego, C;Metzger, M;

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

Discovery of novel 1, 2, 4-thiadiazole derivatives as potent, orally active agonists of sphingosine 1-phosphate receptor subtype 1 (S1P1)

Ren, F;Deng, G;Wang, H;Luan, L;Meng, Q;Xu, Q;Xu, H;Xu, X;Zhang, H;Zhao, B;Li, C;Guo, TB;Yang, J;Zhang, W;Zhao, Y;Jia, Q;Lu, H;Xiang, J;Elliott, JD;Lin, X;

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

Diabetes impairs cortical plasticity and functional recovery following ischemic stroke

Sweetnam, D;Holmes, A;Tennant, KA;Zamani, A;Walle, M;Jones, P;Wong, C;Brown, CE;

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

ATF3 protects against atherosclerosis by suppressing 25-hydroxycholesterol-induced lipid body formation

Gold, ES;Ramsey, SA;Sartain, MJ;Selinummi, J;Podolsky, I;Rodriguez, DJ;Moritz, RL;Aderem, A;

Product: LPS from Salmonella minnesota R595 (Re)

  • Cell culture:

    Cells were cultured at 37C and in 5% CO2 in a humidified incubator. Primary mouse BMDMs were prepared as previously described (Gilchrist et al., 2006). In brief, femoral BM cells were plated on nontissue culturetreated plastic in BMDM medium … On day 7, cells were stimulated as indicated in the Results section, before being used for microscopy, flow cytometry, RNA extraction, or lipid extraction. Stimuli that were introduced into BMDM medium (as indicated in the text) were as follows: LPS (from Salmonella minnesota; List Biological Laboratories), …

Transcutaneous immunization with a Vibrio cholerae O1 Ogawa synthetic hexasaccharide conjugate following oral whole-cell cholera vaccination boosts vibriocidal responses and induces protective immunity in mice

Tarique, AA;Kalsy, A;Arifuzzaman, M;Rollins, SM;Charles, RC;Leung, DT;Harris, JB;Larocque, RC;Sheikh, A;Bhuiyan, MS;Saksena, R;Clements, JD;Calderwood, SB;Qadri, F;Kovc, P;Ryan, ET;

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

  • Boosting immunization of mice.

    On day 117, we randomly assigned primed mice in one of several cohorts to receive a boosting vaccination (Table 1). Some cohorts received CHO-BSA (10 g saccharide/immunization/mouse) transcutaneously (TCI) with or without 25 g of immunoadjuvantative cholera toxin (CT; List Biological Laboratories, Campbell, CA) or E. coli heat-labile toxin (LT) (9). We immunized additional cohorts with CHO-BSA (10 g saccharide/immunization/mouse) subcutaneously (SCI) with or without 5 g of immunoadjuvantative CT. … Control mice received CT or LT boosting alone or no boosting immunizations following oral priming. Additional control cohorts received no priming oral immunization and received only CHO-BSA with CT or LT transcutaneously or subcutaneously. When booster doses were given, they were administered at 2-week intervals for a total of four immunizations. Transcutaneous immunizations were carried out as previously described (32).

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