Citations

Bacterial Toxin Research Citations

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4918 total record number 290 records this year

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4918 citations found

Lysophosphatidic acid increases proximal tubule cell secretion of profibrotic cytokines PDGF-B and CTGF through LPA2- and Gq-mediated Rho and v6 integrin-dependent activation of TGF-

Geng, H;Lan, R;Singha, PK;Gilchrist, A;Weinreb, PH;Violette, SM;Weinberg, JM;Saikumar, P;Venkatachalam, MA;

Product: Pertussis Toxin from B. pertussis (in Glycerol)

Characterization of a multi-component anthrax vaccine designed to target the initial stages of infection as well as toxaemia

Cote, CK;Kaatz, L;Reinhardt, J;Bozue, J;Tobery, SA;Bassett, AD;Sanz, P;Darnell, SC;Alem, F;O'Brien, AD;Welkos, SL;

Product: Anthrax Protective Antigen (PA), Recombinant from B. anthracis

  • Vaccine formulations:

    The vaccines discussed in this report were composed of rPA (List Biological Laboratories), recombinant spore-specific proteins produced as described earlier ( Brahmbhatt et al., 2007 ; Cybulski et al., 2008 ; Mikesell et al., 1983 ) or a combination of the antigens. The specific amounts of antigens used in the vaccine formulations are described in the figure legend of each experiment. Aluminium hydroxide gel (AL; aluminium content per vaccination ~125 g for mice or ~500 g for guinea pigs) or the Sigma adjuvant system (SAS) was used as adjuvant (Sigma Aldrich). SAS is an emulsion of monophosphoryl lipid A and trehalose dicorynomycolate, which may promote mixed T helper 1 (Th1)/Th2 immune responses to vaccines, and was used as directed by the manufacturer.

Essential role of integrin-linked kinase in regulation of phagocytosis in keratinocytes

Sayedyahossein, S;Nini, L;Irvine, TS;Dagnino, L;

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

Product: SNAPtide® Peptide Substrate (o-Abz/Dnp) for C. botulinum Type A Neurotoxin

  • Materials:

    SNAPtide(o-Abz-Dnp) was purchased from List Biological Laboratory. …

    SNAPtide based LC activity assay:

    SNAPtide (o-Abz-Dnp) (List Biological Laboratories) was used for studying the LCs
    activity and inhibition (Figure 2.2). 100 M SNAPtide stock was prepared in DMSO.
    The proteolytic reaction was initiated by the addition of LC to 20 mM HEPES (pH 7.5)
    with 2 M SNAPtide. The protease activity was monitored by the increase of o-Abz
    fluorescence (ex: 320 nm, em: 420 nm). The results were analyzed using Sigmaplot. …

Toll-like receptor-induced inflammatory cytokines are suppressed by gain of function or overexpression of G(i2) protein

Li, P;Neubig, RR;Zingarelli, B;Borg, K;Halushka, PV;Cook, JA;Fan, H;

Product: ULTRA PURE LPS from Escherichia coli O111:B4

  • Cell culture and stimulation:

    … RAW 264.7 cells expressing Gi2 and -galactosidase were stimulated with LPS (10ng/ml, ultra-pure LPS from Escherichia coli O111:B4, List Laboratories, Campbell, CA), Pam3CSK4 (1g/ml, Invivogen) or Poly (I:C) (10g/ml Invivogen) for 24 hours. LPS-induced TNF and IL-6 production were analyzed by enzyme-linked immunosorbant assay (ELISA). …

Aberrant accumulation of interleukin-10-secreting neutrophils in TRAF2-deficient mice

Piao, JH;Yagita, H;Okumura, K;Nakano, H;

Product: LPS from Salmonella minnesota R595 (Re)

  • Reagents and cell culture:

    LPS (R595) (List Biological Laboratories, Inc., Campbell, CA, USA), …

    Flow cytometry:

    … For intracellular cytokine staining, cells were incubated with LPS (100ngml1) in the presence of GolgiStop (2M; BD Biosciences) for 5h. Surface and intracellular cytokine staining were performed as described elsewhere.25 In some experiments, BM cells were stimulated with LPS (100ngml1) or Pam3CS(K)4 (100ngml1) for 24h in the absence or presence of anti-TNF antibody (10gml1), and were subjected to intracellular cytokine staining.

Cooperation between classical and alternative NF-B pathways regulates proinflammatory responses in epithelial cells

Tully, JE;Nolin, JD;Guala, AS;Hoffman, SM;Roberson, EC;Lahue, KG;van der Velden, J;Anathy, V;Blackwell, TS;Janssen-Heininger, YM;

Product: Unspecified List Labs LPS

  • Cell Culture:

    Primary murine tracheal epithelial cells (MTECs) were isolated and cultured … Sixteen hours before treatment, cells were starved in medium containing 0.5% FBS. Cells were exposed to 1 g/ml LPS (List Biological Laboratories, Inc., Campbell, CA), …

    Mice

    C57Bl/6 mice were anesthetized and received 5 g LPS oropharyngeally (List Biological Laboratories, Inc.), and 24 hours later were killed by pentobarbital injection. The right lobe was flash-frozen in liquid nitrogen and pulverized, and the left lobe was inflated with 4% paraformaldehyde. Five-micron sections were used to assess the localization of RelB in situ via immunofluorescence, …

    Author did not specify which List Labs LPS product was utilized in their research.  List Labs provides the following LPS products:  https://listlabs.com/product-information/lipopolysaccharides/

Cortical dynein is critical for proper spindle positioning in human cells.

Kotak, S;Busso, C;Gnczy, P;

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

  • Plasmids and RNAi:

    … Depletion of Rae1 was performed using a double-stranded siRNA oligonucleotide with the sequence 5-CUCAGCAGUAACCAAGCGAUACAGA-3 (Rae1 siRNA; Stealth RNAi; Invitrogen). Cells were incubated with pertussis toxin (181214A1; List Biological Laboratories, Inc.) at 400 ng/ml for 4 h before analysis.

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

Antibody nanoparticle dispersions formed with mixtures of crowding molecules retain activity and in vivo bioavailability

Miller, MA;Khan, TA;Kaczorowski, KJ;Wilson, BK;Dinin, AK;Borwankar, AU;Rodrigues, MA;Truskett, TM;Johnston, KP;Maynard, JA;

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

Multicolored stain-free histopathology with coherent Raman imaging

Freudiger, CW;Pfannl, R;Orringer, DA;Saar, BG;Ji, M;Zeng, Q;Ottoboni, L;Wei, Y;Ying, W;Waeber, C;Sims, JR;De Jager, PL;Sagher, O;Philbert, MA;Xu, X;Kesari, S;Xie, XS;Young, GS;

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