Citations

Citations

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Page 156 out of 479
4784 citations found

Glutamatergic Input Varies with Phrenic Motor Neuron Size

Rana, S;Mantilla, CB;Sieck, GC;

Product: Anti-Cholera Toxin B Subunit (Goat)

DPP8/9 inhibitors are universal activators of functional NLRP1 alleles

Gai, K;Okondo, MC;Rao, SD;Chui, AJ;Ball, DP;Johnson, DC;Bachovchin, DA;

Product: Anthrax Lethal Factor (LF), Recombinant from B. anthracis

  • Reagents and antibodies

    … For cell culture experiments, Val-boroPro was resuspended in DMSO containing 0.1% TFA to prevent compound cyclization. Anthrax Lethal Factor (Catalog #172B) and PA (Catalog #171E) were purchased from List Labs, …

    LDH cytotoxicity assays

    For LDH release experiments involving primary macrophages, mBMDM and rBMDM were isolated from the femurs and tibias of 79-week-old male and female mice and 712-week-old male rats. 1107 cells were plated on 10cm Petri dishes. mBMDMs were differentiated in DMEM with 10% FBS and 20% L Cell medium for 6 days and rBMDMs in 30% L Cell medium for 79 days. Macrophages were scraped and reseeded at 0.25106 cells/well in 12-well plates in Opti-MEM and incubated overnight before treatment. Cells were then treated as indicated with compounds or LT. …

    In vitro and in cell LF cleavage assays

    HEK 293T cells were seeded at 0.5106 cells/well in six-well plates and transiently transfected with 2g of the indicated plasmids using FuGENE HD. For the in vitro assay, lysates were harvested after 48h and normalized to 1mg/mL using the DC Protein Assay kit (Bio-Rad). These lysates were then incubated with LF (1g/mL) for the indicated time periods at 25C quenched by boiling with 2SDSPAGE sample buffer at the indicated times, separated by SDSPAGE, immunoblotted, and visualized using the Odyssey Imaging System (Li-Cor). For the in cell assay, after 48h after transfection cells were treated with LT (1g/mL, 6h) before lysates were harvested for immunoblotting as described above.

Salivary gland macrophages assist tissue-resident CD8+ T cell immune surveillance

Stolp, B;Thelen, F;Ficht, X;Altenburger, L;Ruef, N;

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

Non-Crh Glutamatergic Neurons in Barrington’s Nucleus Control Micturition via Glutamatergic Afferents from the Midbrain and Hypothalamus

Verstegen, AMJ;Klymko, N;Zhu, L;Mathai, JC;Kobayashi, R;Venner, A;Ross, RA;VanderHorst, VG;Arrigoni, E;Geerling, JC;Zeidel, ML;

Product: Anti-Cholera Toxin B Subunit (Goat)

Cholera toxin promotes pathogen acquisition of host-derived nutrients

Rivera-Chvez, F;Mekalanos, JJ;

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

Utilization of lipopolysaccharide challenge in cynomolgus macaques to assess IL-10 receptor antagonism

Kamperschroer, C;Goldstein, R;Schneider, PA;Kuang, B;Eisenbraun, MD;

Product: ULTRA PURE LPS from Escherichia coli O111:B4

  • LPS:

    Ultrapure-grade LPS prepared from Escherichia coli 0111:B4 (List Biologicals, Campbell, CA) was reconstituted in sterile saline at 10g/ml and stored in aliquots at 20C until use in experiments. The specific bioactivity for the individual lot (4216A2) used for this work was not available, but the predicted activity provided by the vendor based on a similar lot was 6.75106 EU/mg (communication from List Biologicals).

    In vitro LPS challenge:

    Whole blood was collected from animals into sodium heparin tubes (Beckton Dickinson, Caanan, CT) to prevent coagulation. Aliquots (200l) of each blood sample were dispensed into 96-well polypropylene plates and placed at 37C and 5% CO2 for 30min. LPS diluted in sterile saline or saline only (control) was added to sample wells (10l volume) to achieve final LPS concentrations ranging from 0 to 10g/ml. The plates were incubated for an additional 5h at 37C and then centrifuged at 4C for 10min at 600g to pellet the cells. Plasma collected from each well was stored at 80C until analyzed. The concentration of TNF in each plasma sample was measured by ELISA using the Monkey TNF ELISA kit (U-CyTech, Utrecht, the Netherlands) according to manufacturer instructions. All samples were measured in duplicate.

    In vivo LPS challenge and antibody-based modulation:

    Animals (n=3/group) were injected IV with 1.0g LPS/kg in a volume of 0.1ml/kg. The LPS was first administered on three different days each separated by a 3-week rest period to establish baseline LPS responses. Prior to the third LPS challenge, blood samples were collected to perform the in vitro LPS challenge (described above) in order to compare in vitro cytokine responses to those induced in vivo. Following another 3-week rest period, animals were injected IV with 0.1, 1, or 10mg/kg of anti-IL-10R1 mAb or with 10mg/kg of the isotype control mAb 2h before a fourth LPS challenge was administered IV. An additional set of control animals was given 10mg/kg anti-IL-10R1 mAb IV and left unchallenged (no LPS). After another 3-week rest period, a fifth and final LPS challenge was performed on all groups.

    Blood samples were collected into serum separator tubes (Greiner Bio-One, Monroe, NC) just prior to and 1, 2, 4, 6, and 24h after each LPS challenge to measure concentrations of cytokines (all timepoints) and C-reactive protein (CRP) (pre-challenge and 24h post-challenge only). Blood samples were also collected just prior to and 0.25, 2, 7, 24, 30, 48, 72, 144, 240, 384, and 552h immediately after antibody administration to measure serum anti-IL10R mAb levels. Sera prepared from the blood samples by centrifugation were stored at 80C (for cytokine and CRP assays) or at 20C (for antibody assay) until thawed and analyzed.

Human endogenous retrovirus HERV-K (HML-2) RNA causes neurodegeneration through Toll-like receptors

Dembny, P;Newman, AG;Singh, M;Hinz, M;Szczepek, M;

Product: Unspecified List Labs LPS

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

MOG-reactive B cells exacerbate the severity of CD4+ T cell-driven CNS autoimmunity

Doss, PMIA;Yeola, AP;Mailhot, B;Baillargeon, J;

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

Nitration of Drp1 provokes mitophagy activation mediating neuronal injury in experimental autoimmune encephalomyelitis

Li, W;Feng, J;Gao, C;Wu, M;Du, Q;Tsoi, B;Wang, Q;Yang, D;Shen, J;

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