Citations

Bacterial Toxin Research Citations

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4918 total record number 290 records this year

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Page 102 out of 492
4918 citations found

Galectin-3 modulates microglia inflammation in vitro but not neonatal brain injury in vivo under inflammatory conditions

Sävman, K;Wang, W;Rafati, AH;Svedin, P;Nair, S;Golubinskaya, V;Ardalan, M;Brown, KL;Karlsson-Bengtsson, A;Mallard, C;

Product: ULTRA PURE LPS from Escherichia coli O55:B5

  • LPS was obtained from List Biological Laboratories, INC. (#423, California, USA). …

    In vitro stimulation:

    At the day of experiments the cell medium was replaced by pre-warmed 500 µL DMEM/antibiotics per well. Cells were stimulated with LPS (10ng/ml), TNF-α (1, 20, 100 ng/ml), IL-1β (1, 20, 100 ng/ml), galectin-3 (5, 50 or 100 ug/mL), or the combinations of LPS (10 ng/ml) or TNF-α (100 ng/mL) with galectin3 (5 ug/ml or 100 ug/ml) for 24 h. Cell culture media from each well was collected and stored at -80°C until analysis. Each experiment was repeated at three independent times using 6 animals/repeat. Vehicle and treatment wells were situated on the same plate and two samples for each treatment were analyzed for every repeat. …

    Product #423 – ULTRA PURE LPS from Escherichia coli O55:B5

Appearance of Claudin-5+ Leukocyte Subtypes in the Blood and CNS During Progression of EAE

Krajewski, D;Paul, D;Ge, S;Jellison, E;Pachter, J;

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

Label-free and Rapid Detection of Anthrax Protective Antigen by Surface-enhanced Raman Scattering on Au Nanorods

Li, B;Wang, T;Bai, W;Su, Q;Wu, X;Dong, P;

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

Structural specificities of cell surface β-glucan polysaccharides determine commensal yeast mediated immuno-modulatory activities

Lee, C;Verma, R;Byun, S;Jeun, EJ;Kim, GC;Lee, S;Kang, HJ;Kim, CJ;Sharma, G;Lahiri, A;Paul, S;Kim, KS;Hwang, DS;Iwakura, Y;Speciale, I;Molinaro, A;De Castro, C;Rudra, D;Im, SH;

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

Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding

Han, Y;Xia, G;Srisai, D;Meng, F;He, Y;Ran, Y;He, Y;Farias, M;Hoang, G;Tóth, I;Dietrich, MO;Chen, MH;Xu, Y;Wu, Q;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Ablation of AgRP neurons

    To ablate AgRP neurons, mice carrying the AgrpDTR/+ allele, were bilaterally microinjected with DT (0.4 ng/side/mouse, List Biological Laboratories, Campbell, CA) using a needle (Hamilton Small Hub RN 33 G, Reno, NV) connected with a 10 μl syringe (Hamilton 700 Microliter, Reno, NV), at a rate of 0.1 μl/min. A total 0.4 μl volume/side was delivered into the dlDRN2. To describe the expression profile of AgRPARC-dlDRN neurons, the vehicle (0.9% NaCl) or DT were injected into the dlDRN with AgrpDTR/+::NpyGFP mice. …

    Product #150 – Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Distinctive waves of innate immune response in the retina in experimental autoimmune encephalomyelitis

Cruz-Herranz, A;Oertel, FC;Kim, K;Cantó, E;Timmons, G;Sin, JH;Devereux, M;Baker, N;Michel, B;Schubert, RD;Rani, L;Cordano, C;Baranzini, SE;Green, AJ;

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

  • In vivo retinal monitoring in EAE

    Mice. For experiments involving in vivo retinal imaging, CX3CR1GFP/+–knock-in mice were fully backcrossed into C57BL/6J. We confirmed the absence of an RD8 mutation (associated with hereditary macular degeneration). In CX3CR1GFP/+–knock-in mice, microglia, macrophages, monocytes, and NK cells express GFP, which can be imaged through CSLO (14), without any immunologic alterations (15).

    Induction and clinical scoring of MOG35-55 EAE. Seven female mice at 10 weeks of age were immunized s.c. with 100 μg of MOG35–55 peptide (Genemed Synthesis) in complete Freund’s adjuvant containing 400 μg Mycobacterium tuberculosis H37Ra (Difco Laboratories). Mice received 200 ng pertussis toxin (List Biological) by i.p. injection at the time of and after immunization. We monitored clinical scores, as described before (42). …

    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)

Hemolysis-associated phosphatidylserine exposure promotes polyclonal plasmablast differentiation

Vijay, R;Guthmiller, JJ;Sturtz, AJ;Crooks, S;Johnson, JT;Li, L;Lan, LY;Pope, RL;Chen, Y;Rogers, KJ;Dutta, N;Toombs, JE;Wilson, ME;Wilson, PC;Maury, W;Brekken, RA;Butler, NS;

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

Brain gray matter astroglia-specific connexin 43 ablation attenuates spinal cord inflammatory demyelination

Une, H;Yamasaki, R;Nagata, S;Yamaguchi, H;Nakamuta, Y;Indiasari, UC;Cui, Y;Shinoda, K;Masaki, K;Götz, M;Kira, JI;

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

  • Induction and clinical evaluation of EAE

    We induced EAE by immunization of mice with 4 mg/ml MOG35–55 peptide (TS-M704-P; MBL, Nagoya, Japan) emulsified in complete Freund’s adjuvant containing 1 mg/ml Mycobacterium tuberculosis H37RA (#231131; BD Difco, Lawrence, KS, USA) at a dose of 200 μg per mouse, followed by intraperitoneal injections of 300 ng pertussis toxin (# 180-A1; List Biological Laboratories Inc., Campbell, CA, USA) per mouse on days 0 and 2. …

    Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Involvement of microRNA-155 in the mechanism of electroacupuncture treatment effects on experimental autoimmune encephalomyelitis

Zhao, P;Chen, X;Han, X;Wang, Y;Shi, Y;Ji, J;Lei, Y;Liu, Y;Kong, Q;Mu, L;Wang, J;Zhao, W;Wang, G;Liu, X;Zhang, T;Zhang, Y;Sun, B;Liu, Y;Li, H;

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

  • 2.2. Induction and evaluation of EAE

    The EAE inducing antigen employed was myelin oligodendrocyte glycoprotein peptide (MOG35-55). To induce EAE, complete Freund’s adjuvant (CFA) emulsified with an equal volume of phosphate-buffered saline (PBS) containing 250 µg of Mycobacterium tuberculosis strain H37Ra (BD Biosciences, San Jose, CA, USA) and 200 µg of MOG35–55 (MEVGWYRSPFSRVVHLYRNGK) (Wuhan Bioyears gene Biotechnology Inc., China), was injected into the mice subcutaneously in each axillary fossa, on experimental day 0 and day 2, immediately followed by an intravenous injection of pertussis toxin (200 ng, List Biological Laboratories, Inc., Campbell, CA, USA) in the tail vein. The control group received only CFA in place of the EAE induction solution. …

    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)

Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma

Cugurra, A;Mamuladze, T;Rustenhoven, J;Dykstra, T;Beroshvili, G;Greenberg, ZJ;Baker, W;Papadopoulos, Z;Drieu, A;Blackburn, S;Kanamori, M;Brioschi, S;Herz, J;Schuettpelz, LG;Colonna, M;Smirnov, I;Kipnis, J;

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