Citations

Bacterial Toxin Research Citations

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279 citations found

Acidity induces durable enhancement of Treg cell suppressive functions for tumor immune evasion

Mani, NL;Weinberg, SE;Chaudhuri, S;Montauti, E;Tang, A;Iyer, R;Fang, D;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • … FoxP3DTR mice to receive transferred Treg cells were treated with 50 mg/kg diphtheria toxin (DT) (List Labs, 150) starting from 5 days prior to tumor inoculation and for every 3 days until time of euthanization. Mice were monitored daily for tumor growth. Tumor volume was measured through digital calipers along the x, y, and z axes and calculated as (xyz)/2. Mice were to be euthanized if tumors exceeded size limit agreed by the Institutional Review Board (IRB), however no animal reached this volume during the duration of the experiment. …

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

Splenic CD169 + Tim4 + Marginal Metallophilic Macrophages Are Essential for Wound Healing After Myocardial Infarction

Ismahil, MA;Zhou, G;Gao, M;Bansal, SS;Patel, B;Limdi, N;Xie, M;Antipenko, S;Rokosh, G;Hamid, T;Prabhu, SD;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

A Live Tracker of Dormant Disseminated Tumor Cells

Landum, F;Correia, AL;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • 2.5 Construction of lipodystrophy mouse model and ibuprofen treatment

    … To induce deletion of Cre-positive cells, mice were injected daily with 100 ng/mouse/day of diphtheria toxin (DT) (Biological List Laboratories, Cat#150) for 5 days via the intraperitoneal (i.p.) route. The R26-(SA-LSL-DTR) flox/flox mice received an equal amount of PBS as the control group. Samples were collected at day 7 after the first injection (Figure 2E). To determine the effect of ibuprofen on lipodystrophy metabolic dysfunction, 1 mg/mL ibuprofen (Sigma, St. Louis, I1892) was continuously added to the drinking water of both Con + IBU and DTRADQ + IBU groups of mice 7 days prior to intraperitoneal injection until the end of the experiment. After 7 days of IBU pretreatment (D−7 to D0), mice in both the DTRADQ + water and DTRADQ + IBU groups were intraperitoneally injected with DT daily for 5 consecutive days (D0 to D4), and at the same time, mice in the Con + water and Con + IBU groups were injected with an equal volume of PBS. All mice were sacrificed to harvest for tissues on D6 (Figure 4A).

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

CD11c-expressing microglia are transient, driven by interactions with apoptotic cells

Ghena, N;Anderson, S;Roberts, J;Irvin, E;Schwakopf, J;Bosco, A;Vetter, M;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

FOXP3+ Regulatory T Cells Require TBET to Regulate Activated CD8+ T Cells During Recovery from Influenza Infection

Mambetsariev, N;Acosta, MAT;Liu, Q;Flores, CPR;Joudi, AM;Helmin, KA;Gurkan, JK;Steinert, EM;Morales-Nebreda, L;Singer, BD;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Diphtheria toxin treatment and adoptive transfer of Treg cells to Foxp3DTR mice

    For the Treg cell depletion studies, Foxp3DTR mice were intra-peritoneally injected with a diphtheria toxin (DT, List Biologicals cat. no. 150) loading dose (50 μg/kg) on day 14 post-influenza virus inoculation and given three maintenance doses (10 μg/kg) every other day thereafter to deplete endogenous Treg cells. For the adoptive transfer experiments, Foxp3DTR mice received a DT loading dose one day before influenza virus inoculation as well as 1 x 106 Treg cells via retro-orbital adoptive transfer from either Black 6 or TBET KO mice enriched using the Miltenyi Biotec CD4+ CD25+ Regulatory T Cell Isolation Kit (cat. no. 130-091-041) according to the manufacturer’s instructions. Foxp3DTR mice receiving adoptive transfers were then given a DT maintenance dose every other day until tissue harvest.

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

AAV-mediated Gene Cocktails Enhance Supporting Cell Reprogramming and Hair Cell Regeneration

Zhang, L;Chen, X;Wang, X;Zhou, Y;Fang, Y;Gu, X;Zhang, Z;Sun, Q;Li, N;Xu, L;Tan, F;Chai, R;Qi, J;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Animals and Genotyping

    In this paper, the different mice including wild-type C57BL/6J mice, transgene Lgr5-EGFPcreERT2 mice (Jackson Laboratory), Sox9 creERT2 mice (Jackson Laboratory), and Rosa26-CAG-tdTomato mice (Jackson Laboratory) were used. In P1-2 mice, the Cre recombination enzyme was activated by intraperitoneal injection of tamoxifen (Sigma, T5648), and the dose was controlled at 0.3 mg/4 g. Diptheria toxin (List Biologicals Lab) was intraperitoneally injected into P4 mice at a dose of 10 ng g−1. …

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

FGD5 in basal cells induces CXCL14 secretion that initiates a feedback loop to promote murine mammary epithelial growth and differentiation

Zhang, T;Zhao, C;Li, Y;Wu, J;Wang, F;Yu, J;Wang, Z;Gao, Y;Zhao, L;Liu, Y;Yan, Y;Li, X;Gao, H;Hu, Z;Cui, B;Li, K;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Foxp3+ Treg control allergic skin inflammation by restricting IFN-γ-driven neutrophilic infiltration and NETosis

Tong, X;Kim, S;Che, L;Park, J;Lee, J;Kim, T;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

Availability of an inflammatory macrophage niche drives phenotypic and functional alterations in Kupffer cells

Huang, H;Chen, Y;Zheng, X;Yue, J;Ju, H;Shi, Y;Tian, L;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

  • Tamoxifen and diphtheria toxin treatment

    Tamoxifen (MedChemExpress) was dissolved in corn oil (20 mg ml−1) and heated at 37°C for 3 hours. To activate Cx3cr1CreERT2-mediated recombinase, each mouse was injected with Tamoxifen (100 mg/kg body weight) by oral gavage every three days, starting from Day 12 post-intraportal injection, as indicated in Fig. 2e. For proliferation tracing experiment, DreERT2-mediated recombinase was introduced by a single dose of tamoxifen gavage (100 mg/kg body weight) on Day 12 post-intraportal injection, as indicated in Fig. 3f. For KC specific depletion, DreERT2-mediated recombinase was introduced by 8 doses of tamoxifen gavage (2 mg per dose), as indicated in Fig. 5d. A single dose of 200 ng DT (List Laboratories) was intraperitoneally introduced one week after the last Tamoxifen injection. The cancer cells were inoculated into liver through portal vein one day after DT injection.

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