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.

4917 total record number 289 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 148 out of 492
4917 citations found

An Apoptotic Caspase Network Safeguards Cell Death Induction in Pyroptotic Macrophages

de Vasconcelos, N;Van Opdenbosch, N;Van Gorp, H;Martn-Prez, R;Zecchin, A;Vandenabeele, P;Lamkanfi, M;

Product: Anthrax Lethal Factor (LF), Recombinant from B. anthracis

Neutrophil-selective deletion of Cxcr2 protects against CNS neurodegeneration in a mouse model of multiple sclerosis

Khaw, YM;Cunningham, C;Tierney, A;Sivaguru, M;Inoue, M;

Product: Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)

  • EAE induction

    To induce EAE disease, complete Freund’s adjuvant, CFA (#F5881, Sigma) containing 400 μg Mycobacterium tuberculosis, Mtb (#DF3114-33-8, Fisher), and 100 μg myelin oligodendrocyte glycoprotein 35–55 peptide (MOG35–55, United Peptides) were subcutaneously administered at 0 and 7 days post-induction (dpi). Pertussis toxin (200 ng/mouse) (#181, List Biological Laboratories, Inc.) was administered on days 0, 2, and 7 dpi. …

    Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)

Methionine Metabolism Shapes T Helper Cell Responses through Regulation of Epigenetic Reprogramming

Roy, DG;Chen, J;Mamane, V;Ma, EH;Muhire, BM;Sheldon, RD;Shorstova, T;Koning, R;Johnson, RM;Esaulova, E;Williams, KS;Hayes, S;Steadman, M;Samborska, B;Swain, A;Daigneault, A;Chubukov, V;Roddy, TP;Foulkes, W;Pospisilik, JA;Bourgeois-Daigneault, MC;Artyomov,

Product: Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)

Short-Chain Alcohols Upregulate GILZ Gene Expression and Attenuate LPS-Induced Septic Immune Response

Ng, H;Jennings, S;Nelson, S;Wang, G;

Product: LPS from Escherichia coli O111:B4

  • Reagents

    Lipopolysaccharide (E. coli, serotype O111:B4 L2630) was from List Biological Laboratories (Campbell, CA) …

    Alcohol Exposure and LPS Challenge

    Mice were exposed to ethanol (2 or 4 g/kg), propanol (2 g/kg), isopropanol (2 g/kg) or PBS via intraperitoneal injection. One hour later, a lethal dose of LPS (10 mg/kg, i.p.) was injected. Animals were monitored every 2 h for 36 h post LPS injection.

    Product #201 – LPS from Escherichia coli O111:B4

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

NRF2 negatively regulates primary ciliogenesis and hedgehog signaling

Liu, P;Dodson, M;Fang, D;Chapman, E;Zhang, DD;

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

MAFG-driven astrocytes promote CNS inflammation

Wheeler, MA;Clark, IC;Tjon, EC;Li, Z;Zandee, SEJ;Couturier, CP;Watson, BR;Scalisi, G;Alkwai, S;Rothhammer, V;Rotem, A;Heyman, JA;Thaploo, S;Sanmarco, LM;Ragoussis, J;Weitz, DA;Petrecca, K;Moffitt, JR;Becher, B;Antel, JP;Prat, A;Quintana, FJ;

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

Specific Detection of Anthrax Infection

Shine, N.; Suryadi, K.

Product: Anthrax Lethal Factor (LF-A), Recombinant from B. anthracis Native Sequence

  • Materials and Methods

    Anthrax lethal factor, Product #169 and MAPKKide® Plus, Prod #532 are from List Biological Laboratories,
    Inc.
    The 96-well, black, flat bottom, nonbinding plates used for the fluorescent plate assay were from
    Corning (cat # 3991). The filtered adult bovine plasmas: Na-Citrate, cat #7310806; K2-EDTA, cat #7310807;
    K3-EDTA, cat #7310808; Li-Heparin, cat #7310810 ; Na-Heparin, cat #7310811; and the filtered adult bovine
    serum cat #7330800 were purchased from Lampire Biological Laboratories.

    Sample Preparation: Stock solutions of the fluorogenic substrate, MAPKKide® Plus, were made 1.25 mM
    in DMSO. The substrate was then diluted 5-fold to 250 µM in assay buffer: 20 mM HEPES, pH 8.0 containing
    0.1% Tween-20.

    LF Activity Assay: LF was spiked into each plasma or serum sample and then each was diluted 1:5 using
    assay buffer. The reaction was initiated by addition of 10 μM MAPKKide® Plus directly to the 1:5 diluted
    plasma or serum, and the assays were run at 37°C using the kinetic mode of the plate reader with readings
    at 1-minute intervals. The samples were run in triplicate with 9 replicate blanks. The limit of detection was
    calculated from the normal distribution of the blank samples (mean + 3 stdev; n = 3 triplicates).

    Product #169L – Anthrax Lethal Factor (LF-A), Recombinant from B. anthracis Native Sequence
    Product #532 – MAPKKide® Plus (AMC) Specific Substrate for Anthrax Lethal Factor

TLR5 participates in the TLR4 receptor complex and promotes MyD88-dependent signaling in environmental lung injury

Hussain, S;Johnson, CG;Sciurba, J;Meng, X;Stober, VP;Liu, C;Cyphert-Daly, JM;Bulek, K;Qian, W;Solis, A;Sakamachi, Y;Trempus, CS;Aloor, JJ;Gowdy, KM;Foster, WM;Hollingsworth, JW;Tighe, RM;Li, X;Fessler, MB;Garantziotis, S;

Product: ULTRA PURE LPS from Escherichia coli O111:B4

  • Exposures

    Mice received ultrapure E. coli O111:B4 LPS (List Biological Labs, Campbell, CA) (50 ml of 1 mg/ml in
    PBS), or control PBS vehicle only, by oropharyngeal aspiration and were phenotyped 24 hr later. For
    systemic LPS exposure, mice received 10 mg/kg LPS or PBS by intraperitoneal injection and were
    phenotyped 24 hr later. …

    Product #421 – ULTRA PURE LPS from Escherichia coli O111:B4

Neuroprotective effect of microglia against impairments of auditory steady-state response induced by anti-P IgG from SLE patients in nave mice

Wang, X;Li, Y;Li, Z;Li, J;Xu, J;Yang, P;Qin, L;

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

  • Breakdown of the BBB and the passive transfer of IgG to mice

    After completing one session of EEG recording under normal conditions, the mice received IgG by passive transfer. Before IgG transfer, the blood–brain barrier was disrupted using a previously described method [35]. In brief, 50 μg complete Freund’s adjuvant (CFA, Sigma-Aldrich, USA) containing heat-killed H37Ra Mycobacterium tuberculosis (Difco, USA) in 50 μl was subcutaneously injected into each of four sites on the hind flank. In addition, mice received an intraperitoneal (i.p.) injection of 200 ng pertussis toxin (PTx, List Biological Laboratories, USA) in 0.2 ml PBS. The injection of PTx was repeated again 3 days later. On the 7th day after the injection of CFA, animals were injected intravenously with PBS (as vehicle) or test or control IgG (200 μg in 0.2 ml PBS). Electrophysiological recording was conducted again 1, 24, 48, and 72 h after the injection of IgG.

    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)