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.

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4784 total record number 156 records this year

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Page 123 out of 479
4784 citations found

Efavirenz as a potential drug for the treatment of triple-negative breast cancers

Chiou, PT;Ohms, S;Board, PG;Dahlstrom, JE;Rangasamy, D;Casarotto, MG;

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

  • … were cultured in complete DMEM-F-12 medium (Gibco) with 5% horse serum (Gibco), 10 g-ml Insulin (Sigma-Aldrich), 20 ng-ml Epidermal Growth Factor (Sigma-Aldrich), 0.5 g-ml Hydrocortisone (Sigma-Aldrich,), and 100 ng-ml Cholera toxin (List Biological

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

Effects of skin-resident regulatory T cells on wound healing after burn injury

Xin, YW;Dong, N;Yao, WU;Chai, YF;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Baseline and Innate Immune Response Characterization of a Zfp30 Knockout Mouse Strain

Laudermilk, L;Tovar, A;Homstad, A;Thomas, J;McFadden, K;Tune, M;Cowley, D;Mock, J;Ideraabdullah, F;Kelada, S;

Product: Unspecified List Labs LPS

  • Neutrophil Recruitment Models

    Lipopolysaccharide (LPS) challenge: Intratracheal instillation of LPS from E. coli (LIST Biologicals Campbell, CA) into lungs of Zfp30+/+ and Zfp30-/- mice was carried out at a dose of 0.3 mg per kg of body weight using previously described methods (Limjunyawong et al. 2015, Mock et al. 2020). …

    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/

P2Y6 Deficiency Enhances Dendritic Cell-Mediated Th1-Th17 Differentiation and Aggravates Experimental Autoimmune Encephalomyelitis

Li, Z;He, C;Zhang, J;Zhang, H;Wei, H;Wu, S;Jiang, W;

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

Impact of Regulatory T Cells on Type 2 Alveolar Epithelial Cell Transcriptomes during Resolution of Acute Lung Injury and Contributions of IFN-γ

Mock, JR;Dial, CF;Tune, MK;Gilmore, RC;O'Neal, WK;Dang, H;Doerschuk, CM;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Salicylanilide Analog Minimizes Relapse of Clostridioides difficile Infection in Mice

Blake, S;Thanissery, R;Rivera, AJ;Hixon, MS;Lin, M;Theriot, CM;Janda, KD;

Product: Toxin A from Clostridium difficile

Leptin increases sympathetic nerve activity via induction of its own receptor in the paraventricular nucleus

Shi, Z;Pelletier, NE;Wong, J;Li, B;Sdrulla, AD;Madden, CJ;Marks, DL;Brooks, VL;

Product: Anti-Cholera Toxin B Subunit (Goat)

OnabotulinumtoxinA Displays Greater Biological Activity Compared to IncobotulinumtoxinA, Demonstrating Non-Interchangeability in Both In Vitro and In Vivo Assays

Rupp, D;Nicholson, G;Canty, D;Wang, J;Rhaume, C;Le, L;Steward, LE;Washburn, M;Jacky, BP;Broide, RS;Philipp-Dormston, WG;Brin, MF;Brideau-Andersen, A;

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

  • Light-Chain Activity High-Performance Liquid Chromatography (LCA-HPLC) Assay

    … Next, 25 μL of 200 μM SNAPtide 520 (List Biological Laboratories Inc., Campbell, CA, USA) was added to each reaction tube (equivalent to 13.3 μM SNAPtide 520) followed by incubation at 30 °C for 20 h (digestion step). Reactions were quenched following the addition of 25 μL of 5% trifluoroacetic acid (TFA). The contents of each tube were then transferred to HPLC vials for analysis. The fluorescently-labeled cleavage product(s) were separated and detected via a reverse-phase (RP)-HPLC method [28] using a Waters 2695 XE Separations Module and a Waters 2475 Multi λ Fluorescence Detector (Waters Corp., Milford, MA, USA). In brief, 25 µL of cleavage products were loaded onto a Symmetry C18 column (300 Å, 3.5 µm, 4.6 mm × 150 mm; Waters Corp.), maintained at 35 °C. Separation was accomplished using a 10−90% CH3CN (0.1% TFA) gradient for 30 min, with a flow-rate of 1 mL/min. The column effluent was monitored fluorescently (excitation λ = 322 nm, emission λ = 420 nm) to detect the o-aminobenzoic acid fluorophore on the N-terminal cleaved fragment of SNAPtide 520. SNAPtide cleavage product (#529, List Biological Laboratories, Inc.) was utilized to identify retention time of the cleavage product, as #529 is the unquenched calibration peptide for SNAPtide 520 substrate for C. botulinum type A neurotoxin.

    Product #520 – SNAPtide® Peptide Substrate (o-Abz/Dnp) for C. botulinum Type A Neurotoxin
    Product #529 – Unquenched Calibration Peptide for SNAPtide® 520 Substrate for C. botulinum Type A Neurotoxin

Stimulation with FITC-labeled antigens confers B cells with regulatory properties

Planchais, C;Rayes, J;Delignat, S;Pashova, S;Varthaman, A;Pashov, A;Bayry, J;Kaveri, SV;Dimitrov, JD;Lacroix-Desmazes, S;

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

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