Citations

Citations

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Page 161 out of 479
4784 citations found

Rapid Discovery and Characterization of Synthetic Neutralizing Antibodies against Anthrax Edema Toxin

Farcasanu, M;Wang, AG;Uchaski, T;Bailey, LJ;Yue, J;Chen, Z;Wu, X;Kossiakoff, A;Tang, WJ;

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

  • … The column was washed with T205N100P0.1 followed by T205N100P0.1 plus 20 mM imidazole and eluted with T205N100P0.1 with 150 mM imidazole. Peak fractions were pooled and diluted tenfold with T20P0.1, loaded onto a Source Q anion exchange column, and eluted by a 0-1M NaCl gradient. Purified EF was concentrated to approximately 20 mg/mL and frozen at -80C. Protein quantitation was performed using extinction coefficients calculated from the known primary sequence of each protein on the Expasy ProtParam webserver. PA was purchased from List Labs. …

TET1 is an important transcriptional activator of TNF expression in macrophages

Sun, F;Abreu-Rodriguez, I;Ye, S;Gay, S;Distler, O;Neidhart, M;Karouzakis, E;

Product: Unspecified List Labs LPS

  • Cell culture:

    The human monocytic leukemia cell line THP-1 (Cell Lines Service GmbH) was cultured in RPMI supplemented with 10% fetal calf serum (FCS, Life Technologies, Basel, Switzerland) and used below passage 10. THP-1 cells were differentiated into macrophages in the presence of 50 ng/ml phorbol myristate acetate (PMA, Sigma, USA) for 48 hours. THP-1 PMA-derived macrophages were stimulated with 10 ng/ml E. coli LPS (List Biological Laboratories, California) for 2 hours. …

     

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

A Novel Substrate for Specific Detection of Anthrax Infection

Suryadi, K.; Shine, N.

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

  • Materials and Methods

    Anthrax lethal factor (Product #172 or #169), are products of List Biological Laboratories, Inc. The 96-well, black, flat bottom, non binding plates used for the fluorescent plate assay were from Corning (cat # 3991). Bovine plasma (cat # 7310806) was
    purchased from Lampire Biological Laboratories.

    Sample Preparation: Stock solutions of the fluorogenic substrates, MAPKKide® Plus (± biotin), were made 2.5 mM in
    DMSO based on the peptide content determined by elemental analysis. The substrates were diluted in assay buffer: 20 mM
    HEPES, pH 8.0 containing 0.1% Tween-20.

    LF Activity Assays:
    A rapid microplate assay method was evaluated for two ranges of LF: 10 to 1000 pg LF/ml 1:10 diluted bovine plasma and 5 to 250 ng/ml 1:5 diluted bovine plasma. Dilution of the bovine plasma was necessary in order to minimize background.
    For the method detecting higher levels of LF (5 to 250 ng/ml 1:5 diluted bovine plasma), 10 μM MAPKKide Plus was added directly to the 1:5 diluted bovine plasma, and the assays were run at 37°C using the kinetic mode of the plate reader with
    readings at 1 or 3 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 = 9).
    For the range 10 and 1000 pg/ml 1:10 diluted plasma, 1.25 μM MAPKKide Plus was added directly to the diluted bovine
    plasma and the time-dependent increase in fluorescence was monitored at 37°C hourly for 5 hours. For the blank samples
    containing no LF there were 3 sets of quadruplicates and the standard deviation was calculated from these three sets. At
    each time point, the plate was read 5 times to increase the precision of the fluorescence readings. The standard curve was
    analyzed using a linear regression fit forcing the intercept through the mean value of the blanks. The limit of detection was
    calculated from the normal distribution of the blank samples (mean + 3 stdev; n = 3 sets of quadruplicates) and calculated as
    pg LF/ml plasma using the standard curve. Subsequently, 6 data sets were evaluated, 2 data sets per day for 3 consecutive
    days. The data is presented as the average of these 6 data sets, each with 4 replicate samples and 12 replicate blanks. At
    each time point, the plate was read 3 times to increase the precision of the fluorescence readings.

    Product #169L – Anthrax Lethal Factor (LF-A), Recombinant from B. anthracis Native Sequence
    Prodcut #172 – Anthrax Lethal Factor (LF), Recombinant from B. anthracis
    Product #532 – MAPKKide® Plus (AMC) Specific Substrate for Anthrax Lethal Factor

The Alzheimer’s Disease-Associated Protein BACE1 Modulates T Cell Activation and Th17 Function

Hernandez-Mir, G;Raphael, I;Revu, S;Poholek, CH;Avery, L;Hawse, WF;Kane, LP;McGeachy, MJ;

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

Stimulation of alpha 7 nicotinic acetylcholine receptor (7nAChR) inhibits atherosclerosis via immunomodulatory effects on myeloid cells

Ulleryd, MA;Mjrnstedt, F;Panagaki, D;Yang, LJ;Engevall, K;Gutirrez, S;Wang, Y;Gan, LM;Nilsson, H;Michalsson, E;Johansson, ME;

Product: Unspecified List Labs LPS

  • … Samples were challenged with 10 ng mL-1 of lipopolysaccharide (LPS, List Biological Laboratories inc.) and treated with PBS or increasing concentrations of AZ6983, 0.1, 1, 10 or 100 mol L-1. …

     

    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/

Production of the herb Ruta chalepensis L. expressing amyloid -GFP fusion protein

Yoshida, T;Watanabe, Y;Ishiura, S;

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

Connections of the laterodorsal tegmental nucleus with the habenular-interpeduncular-raphe system

Bueno, D;Lima, LB;Souza, R;Gonalves, L;Leite, F;Souza, S;Furigo, IC;Donato, J;Metzger, M;

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

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

  • Subjects:

    Two male macaque monkeys (1 Macaca mulatta (Y), 1 Macaca nemestrina (S)) were used for these experiments. Animal Y was 4 years old and weighed 8.2 kg and Animal S was 6 years old and weighed 17.4 kg at the time of surgery. The subjects used in this study were anatomically typical, with no observable abnormalities. MRI-guided injections of anatomical tracers were performed stereotaxically under sterile conditions. Injection sites, tracers used, and volumes of injection for each case are shown in Table 2.1. The animals received bilateral injections of anterograde tracer (fluoroemerald; FE) in superior colliculus and retrograde tracer (choleratoxin B; CTB) in the lateral nucleus of the amygdala; this yielded 4 hemispheres for anatomical analysis.

    Table 2.2

    Choleratoxin B List Labs

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

Necroptotic cell binding of 2-glycoprotein I provides a potential autoantigenic stimulus in systemic lupus erythematosus

Salem, D;Subang, R;Divangahi, M;Pernet, E;Pineau, C;Cayrol, R;Levine, JS;Rauch, J;

Product: LPS from Escherichia coli O111:B4

Myeloid sphingosine-1-phosphate receptor 1 is important for CNS autoimmunity and neuroinflammation

Tsai, HC;Nguyen, K;Hashemi, E;Engleman, E;Hla, T;Han, MH;

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