Citations

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.

4784 total record number 156 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 350 out of 479
4784 citations found

CD160 isoforms and regulation of CD4 and CD8 T-cell responses

El-Far, M;Pellerin, C;Pilote, L;Fortin, JF;Lessard, IA;Peretz, Y;Wardrop, E;Salois, P;Bethell, RC;Cordingley, MG;Kukolj, G;

Product: Tetanus Toxoid from Clostridium tetani

  • Tetanus toxoid stimulation assay:

    Total PBMCs from healthy donors were thawed in RPMI-1640 medium containing 10% heat-inactivated human serum (GemCell). Cells were washed twice with medium and suspended at a final concentration of 1.5 106 cells/ml. Tetanus toxoid (List Biological Laboratories) was added at a concentration of 2.5g/ml. …

The effect of omeprazole on the development of experimental autoimmune encephalomyelitis in C57BL/6J and SJL/J mice

Sands, SA;Tsau, S;Yankee, TM;Parker, BL;Ericsson, AC;LeVine, SM;

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

Atomic layer deposition coating of carbon nanotubes with aluminum oxide alters pro-fibrogenic cytokine expression by human mononuclear phagocytes in vitro and reduces lung fibrosis in mice in vivo

Taylor, AJ;McClure, CD;Shipkowski, KA;Thompson, EA;Hussain, S;Garantziotis, S;Parsons, GN;Bonner, JC;

Product: ULTRA PURE LPS from Escherichia coli O111:B4

  • Primary Human Monocytes:

    …Cells were allowed to adhere to the plates in an incubator at 37°C, 5% CO2, and 95% relative humidity for 2 hrs. After 2 hrs, the cell culture medium was aspirated, cells were washed with fresh medium and incubated with 5 ng/mL of ultrapure LPS from Escherichia coli O111:B4 (List Biological Laboratories, Inc., Campbell, CA) over night for priming. …

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

The N-terminal Arg residue is essential for autocatalytic activation of a lipopolysaccharide-responsive protease zymogen

Kobayashi, Y;Shiga, T;Shibata, T;Sako, M;Maenaka, K;Koshiba, T;Mizumura, H;Oda, T;Kawabata, S;

Product: LPS from Salmonella minnesota R595 (Re)

  • Materials:

    … Lipopolysaccharides from Salmonella minnesota R595 (Re) were purchased from List Biological Laboratories Inc. (Campbell, CA).  Biotinylation of S. minnesota R595 (Re) lipopolysaccharides was performed using EZ-Link Sulfo-NHS-LC-Biotin…

    Binding Assay to Lipopolysaccharide-immobilized Sepharose:

    Sepharose coupled to streptavidin was incubated for 2 h at 4 C in the presence or absence of 10 g of biotinylated lipopolysaccharides in 1.0 ml of TBS1, and Sepharose, obtained by centrifugation at 6,000 g for 5 min was washed with TBS1. …

    Amidase Activity of Recombinant Proteins Activated by Lipopolysaccharides:

    Recombinant proteins were incubated in the presence of various concentrations of lipopolysaccharides in 100 mm Tris-HCl, pH 8.0, at 37 C for 20 min. …

    Lipopolysaccharide-binding Assay with a Surface Plasmon Sensor:

    Biotinylated lipopolysaccharides (2.3 m in 10 mm Hepes-NaOH, pH 7.4, containing 150 mm NaCl) were immobilized on a sensor chip SA of a BIAcore X system…

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

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

Product: LPS from Escherichia coli O111:B4

  • Materials:

    Escherichia coli O111 B4-derived LPS was obtained from List Biological Laboratories, Inc. (Campbell, CA, USA).

    Northern blot analysis and Cox2 mRNA inhibition:

    The procedure employed was similar to that reported previously (14). Briefly, 106 cells were placed in Falcon 5-cm-diameter dishes (Becton Dickinson Labware, Franklin Lakes, NJ, USA) and pre-treated for 30 min with each of the phenol-related compounds at a concentration of 106 M, 105 M or 104 M. They were then incubated in the presence or absence of LPS (100 ng/ml), and their total RNA was prepared 3 h later by the acid guanidine-phenol-chloroform procedure (15). …  Statistical analyses were performed using Students t-test. Inhibition of LPS-stimulated Cox2mRNA expression byp-cresol, p-cresol dimer, pHA, pHA dimer and BHA in RAW264.7 cells was carried out as follows: The cells were pretreated for 30 min with or without addition of 105Mp-cresol, pHA,p-cresol dimer, pHA dimer or BHA, and then incubated with or without LPS at 100 ng/ml for 3 h. Total RNA was prepared and Cox2 mRNA expression was confirmed by northern blot analysis.

    Preparation of nuclear extract and microwell colorimetric Nfb assay:

    Nuclei were extracted and prepared for the microwell colorimetric Nfb assay. In brief, the cells in 5-cm-diameter Falcon dishes (106cells per dish) were pretreated for 30 min with or without the indicated doses of the compounds, and then treated with LPS at 100 ng/ml for 1 h. …Inhibition of LPS-stimulated Nf-b activation byp-cresol,p-cresol dimer, pHA, pHA dimer or BHA in RAW264.7 cells was carried out as follows: The cells were pretreated for 30 min with or without addition of 105 M p-cresol, pHA, p-cresol dimer, pHA dimer or BHA, and then incubated with or without the LPS at 100 ng/ml for 1 h. Nuclear extracts were prepared and used in a TransAM (Active Motif) ELISA-like assay to quantify the Nfb p50, p52, p65 and RelB DNA-binding activity. …

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

  • … To determine whether antisera induced by CTB or CTBCOMP fusion protein with or without heat treatment inhibit CT from binding its receptor GM1, 100 µl of the serially diluted antisera were incubated with 100 µl of CT (0.4 µg/ml in PBS, List Biological Laboratories, Inc

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

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

Product: Toxin B from Clostridium difficile

  • Inhibition of Rho GTPase activity:

    To study cellular phenotypes independent of GTPase activation, cells were treated with either Clostridium difficile toxin B (TcdB) or C3 transferase to irreversibly inactivate either RhoA, Rac and Cdc42 or RhoA, respectively. Cells were treated wither with 200 ng/ml TcdB (List Biologicals) or 1 g/ml cell-permeable C3 (Cytoskeleton) for 4 hours. Attachment experiments were carried out immediately after toxin treatment.