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.

5002 total record number 30 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 313 out of 501
5002 citations found

Antiphospholipid antibody-mediated effects in an arterial model of thrombosis are dependent on Toll-like receptor 4

Laplante, P;Fuentes, R;Salem, D;Subang, R;Gillis, MA;Hachem, A;Farhat, N;Qureshi, ST;Fletcher, CA;Roubey, RA;Merhi, Y;Thorin, ;Levine, JS;Mackman, N;Rauch, J;

Product: LPS from Escherichia coli O111:B4

Product: LPS from Escherichia coli O111:B4

Melatonin enhances interleukin-10 expression and suppresses chemotaxis to inhibit inflammation in situ and reduce the severity of experimental autoimmune encephalomyelitis

Chen, SJ;Huang, SH;Chen, JW;Wang, KC;Yang, YR;Liu, PF;Lin, GJ;Sytwu, HK;

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

Molecular Dynamics of Multivalent Soluble Antigen Arrays Support a Two-Signal Co-delivery Mechanism in the Treatment of Experimental Autoimmune Encephalomyelitis

Hartwell, BL;Smalter Hall, A;Swafford, D;Sullivan, BP;Garza, A;Sestak, JO;Northrup, L;Berkland, C;

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

CD43 Functions as an E-Selectin Ligand for Th17 Cells In Vitro and Is Required for Rolling on the Vascular Endothelium and Th17 Cell Recruitment during Inflammation In Vivo

Velzquez, F;Grodecki-Pena, A;Knapp, A;Salvador, AM;Nevers, T;Croce, KJ;Alcaide, P;

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

CD11b(+) Mononuclear Cells Mitigate Hyperoxia-Induced Lung Injury in Neonatal Mice

Eldredge, LC;Treuting, PM;Manicone, AM;Ziegler, SF;Parks, WC;McGuire, JK;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Plasmacytoid dendritic cells are dispensable for noninfectious intestinal IgA responses in vivo

Moro-Sibilot, L;This, S;Blanc, P;Sanlaville, A;Sisirak, V;Bardel, E;Boschetti, G;Bendriss-Vermare, N;Defrance, T;Dubois, B;Kaiserlian, D;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • In vivo treatments:

    To deplete pDCs, BDCA2-DTR mice were injected i.p. with 20 ng/g of DT (List Biological Laboratories, Campbell, CA, USA) on day 0 (or day 1 for oral immunization), then every other day with 10 ng/g. DT-treated WT littermates were used as controls. …CD4+ T-cell depletion was controlled in blood at day 0 before starting DT treatment and at sacrifice.

Regeneration in the Pituitary After Cell-Ablation Injury: Time-Related Aspects and Molecular Analysis

Willems, C;Fu, Q;Roose, H;Mertens, F;Cox, B;Chen, J;Vankelecom, H;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • DT treatment and blood sampling of mice:

    GHCre/iDTR mice and Cre-negative control littermates (referred to as /iDTR) of the indicated ages were injected ip with DT (4-ng/g body weight, twice a day at 9 am and 5 pm; List Biological Laboratories) for either 3 (3-d DT treatment [3DT]) or 10 (10DT) consecutive days. Three to 6 mice were used per condition in the independent experiments. …

    Blood samples (100 L) were taken retroorbitally at 9 am, first on the day before the start of DT treatment and then at 11 days (d11), 1.5, 12, and 15 months after DT initiation. …

Product: Cholera Toxin B Subunit (CTB) from Vibrio cholerae FITC, Conjugate

Enzyme replacement for GM1-gangliosidosis: Uptake, lysosomal activation, and cellular disease correction using a novel -galactosidase:RTB lectin fusion

Condori, J;Acosta, W;Ayala, J;Katta, V;Flory, A;Martin, R;Radin, J;Cramer, CL;Radin, DN;

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

  • …To detect GM1 ganglioside, cells were permeabilized, blocked with BSA-glycine, and then incubated with Cholera Toxin B protein (List Biologicals) that had been conjugated to Dylight 594 (CTXB- Dylight 594 ). Cells were subsequently counterstained with 600 nM DAPI and images acquired using the BD Pathway 855 High Content Bioimager (BD Biosciences) as described [24] . …

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