Citations

Bacterial Toxin Research Citations

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5030 total record number 58 records this year

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5030 citations found

Microbial metabolism of food allergens determines the severity of IgE-mediated anaphylaxis

Sánchez-Martínez, E;Rondeau, LE;Garrido-Romero, M;da Luz, BB;Haas, DA;Yuen, G;Hall, P;Dang, R;Wang, XY;Moreno-Serna, L;López-Sanz, C;Nuñez-Borque, E;Garrido-Arandia, M;Diaz-Perales, A;Carrasco, YR;Koenig, JFE;Walker, TD;Jordana, M;Verdu, EF;Surette, MG;Ojeda, P;Vega, F;Blanco, C;Shreffler, WG;Patil, SU;Moreno, FJ;Jiménez-Saiz, R;Caminero, A;

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

  • Food allergy and anaphylaxis model

    To study the impact of microbes on PN metabolism and anaphylaxis, C3H-HeN mice with different microbiota were sensitized to PN using distinct techniques. 1. Intra-gastric sensitization: mice were provided 3.25 mg of crude PN extract (CPE; Greer Laboratories Inc) and 0.625 µg of cholera toxin (List Biological Laboratories) in 0.1 mL of PBS by oral gavage once a week for 6 weeks; 2. Intra-peritoneal sensitization: mice were provided 3.25 mg of CPE and 6.25 µg of cholera toxin in 0.1 mL of PBS intra-peritoneally once a week for 4 weeks; …

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

K27-linked RORγt ubiquitination by Nedd4 potentiates Th17-mediated autoimmunity

Zeng, Q;Guo, H;Tang, N;Renavikar, PS;Karandikar, NJ;Lovett-Racke, AE;Racke, MK;Yan, C;Tang, R;Sinha, S;Ghosh, K;Ryal, JP;Ouyang, S;Chen, M;Amari, F;Vincenzo, C;Pope, RM;Li, Y;Yang, H;Langdon, WY;Zhang, J;

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

Benzoylacetonitrile as a novel anti-inflammatory compound on attenuating microglia and encephalitogenic T cell activation in experimental autoimmune encephalomyelitis

Kuo, PC;Zhao, Z;Scofield, BA;Paraiso, HC;Yu, II;Brown, DA;Yen, JJ;

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

Treponema Denticola Activates NF-?B Pathway via Toll-like Receptor 2

Kokubu, E;Ando, Y;Kikuchi, Y;Yonezawa, H;Ishihara, K;

Product: LPS from Escherichia coli O55:B5

  • 2. Signal evaluation by recognition of T. denticola via TLR2 or TLR4

    Escherichia coli O55:B5 LPS (List Biological Labs, Inc. Ca, USA) was added to TLR4-reporter cells for a positive control. In a preliminary experiment, the phosphatase activity of T. denticola was confirmed to be negligible (data not shown).

    Product #203A – LPS from Escherichia coli O55:B5

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

  • In Vivo Efficacy Study

    The in vivo efficacy of various exosome formulations was assessed using an EAE mouse model, which simulates the pathology of human multiple sclerosis.[50] In brief, an equivalent volume of 2 mg mL−1 MOG35–55 peptides (Prospec, Rehovot, Israel) and Complete Freund’s Adjuvant (CFA), containing 4 mg mL−1 of heat-killed Mycobacterium tuberculosis H37RA (Chondrex, Woodinville, WA), was mixed using a homogenizer (Qiagen, Hilden, Germany). The emulsified MOG peptides were administered subcutaneously at a dose of 200 µg per mouse. In addition, 400 ng of pertussis toxin (List Biological Labs, Campbell, CA) was intraperitoneally administered 2 and 24 h after emulsion injection. …

    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)

Sexual dimorphism during LPS-induced systemic inflammation

Jansen, A;Bruse, N;Waalders, N;Lier, D;Leijte, G;Gerretsen, J;Adriaansen, B;Herwaarden, T;Pickkers, P;Kox, M;

Product: LIST™ HPT™ from Escherichia coli O113

  • Experimental endotoxemia

    Experimental endotoxemia procedures were performed as described extensively elsewhere 34 283 . In short: during both LPS challenge days, subjects were admitted to the research unit of the Intensive Care Department of the Radboud university medical center for 8 hours. Subjects had to refrain from alcohol and caffeine (24 hours), and food and drinks (12 hours) prior to LPS administration. Upon admission, subjects were weighed to determine the total dose of LPS to be administered (1 ng/kg bodyweight). An intravenous cannula was placed in an antebrachial vein to administer fluids and LPS. A radial artery catheter (BD Infusion Therapy Systems, Sandy, USA) was placed under ultrasound guidance to allow serial blood sampling and continuous monitoring and collection of hemodynamic data. Prior to LPS administration, prehydration fluids (1.5 liters of 2.5% glucose / 0.45% sodium chloride in 45 minutes) were administered to reduce the risk of vasovagal responses 49. Thereafter, a bolus of 1 ng/kg LPS (E. coli Type O113, Lot no. 94332B1; List Biological Laboratories, Campbell, USA) …

    To request GMP services for #9433 use the following text…
    Product #9433 – GMP LPS Lipopolysaccharide List™ Hpt™ From Escherichia Coli Type O113

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

Changes in sensory and motor neurons populations following LPC-induced sciatic nerve demyelination in rats: A study using CTB retrograde tracing

Wang, H;Wu, S;Lu, J;Su, Y;Wang, J;Wang, Y;Xu, D;Liu, Y;Gao, J;Bai, W;Cui, J;

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

The transcription factor combination MEF2 and KLF7 promotes axonal sprouting in the injured spinal cord with functional improvement and regeneration-associated gene expression

Attwell, CL;Maldonado-Lasunción, I;Eggers, R;Bijleveld, BA;Ellenbroek, WM;Siersema, N;Razenberg, L;Lamme, D;Fagoe, ND;van Kesteren, RE;Smit, AB;Verhaagen, J;Mason, MRJ;

Product: Anti-Cholera Toxin B Subunit (Goat)

  • Experimental animals and surgical procedures

    … Three days before perfusion, all animals were anesthetized with isoflurane and the left sciatic nerve was exposed. Animals were injected with 3 µl cholera toxin subunit B (CTB; 10 mg/ml) (103B, List Laboratories Inc., Campbell, CA) in the sciatic nerve to transganglionically label ascending dorsal column axons in the spinal cord. …

    To determine the effect of GFP and a conditioning lesion (CL) on axonal regeneration and/or retraction after dorsal column lesion (DCL), we used three groups of 6 animals (GFP/CL/DL, CL/DCL, DCL only). In the GFP/CL/DCL group viral vectors were injected into the left L4 and L5 DRG with dual vectors expressing only GFP (8.1× 1012 GC/ml) (as described above), 4 weeks before the DCL. The GFP/CL/DCL and CL/DCL groups received a CL 7 days prior to DCL. For the CL, animals were anaesthetized with isoflurane, the left sciatic nerve exposed and transected at the mid-thigh level, followed by wound closure. All groups received a DCL and transganglionic tracing with CTB as described above. Where a CL was given, CTB was injected into the proximal stump. Anaesthesia and pain relief were administered as described above. …

    Immunohistochemistry

    … Primary antibodies were as follows. Goat anti-CTB (1:100,000 with 72 h incubation) (List BIological Laboratories); …

    Product #104 – Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt
    Product #703 – Anti-Cholera Toxin B Subunit (Goat)

Hyaluronic acid-curcumin nanoparticles for preventing the progression of experimental autoimmune uveitis through the Keap1/Nrf2/HO-1 signaling pathway

Tang, W;Huang, X;Yi, YD;Cao, F;Deng, M;Fan, J;Jiang, ZX;Tao, LM;Wang, X;Shi, L;

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