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 214 out of 479
4784 citations found

Renitence vacuoles facilitate protection against phagolysosomal damage in activated macrophages

Wong, AO;Marthi, M;Mendel, ZI;Gregorka, B;Swanson, MS;Swanson, JA;

Product: LPS from Salmonella typhimurium

  • Materials:

    LPS from Salmonella typhimuirum (no. 225) was purchased from List Biological Laboratories (Campbell, CA). …

    Cell culture and stimulation:

    …  LPS (100 ng/ml) was added to cells during both the overnight pulse and chase period.  Lysosomal damage was induced by feeding BMM 3 m AW beads in RPMI lacking serum for 60 min.  AW beads were added at a
    concentration empirically determined to result in uptake of on average 3 to 4 beads per cell by
    both resting and LPS-activated BMM.  All analyses of damage were performed on cells that had
    internalized 3 to 7 beads per cell. …

SRC1 promotes Th17 differentiation by overriding Foxp3 suppression to stimulate RORt activity in a PKC–dependent manner

Sen, S;Wang, F;Zhang, J;He, Z;Ma, J;Gwack, Y;Xu, J;Sun, Z;

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

Hydrogen postconditioning promotes survival of rat retinal ganglion cells against ischemia/reperfusion injury through the PI3K/Akt pathway

Wu, J;Wang, R;Yang, D;Tang, W;Chen, Z;Sun, Q;Liu, L;Zang, R;

Product: Cholera Toxin B Subunit (CTB) from Vibrio cholerae FITC, Conjugate

ATG-dependent phagocytosis in dendritic cells drives myelin-specific CD4+ T cell pathogenicity during CNS inflammation

Keller, CW;Sina, C;Kotur, MB;Ramelli, G;Mundt, S;Quast, I;Ligeon, LA;Weber, P;Becher, B;Mnz, C;Lnemann, JD;

Product: Pertussis Toxin from B. pertussis (in Glycerol)

  • EAE:

    On day 0, donor mice were actively induced with EAE via s.c. immunization in the flank region with 200 µg MOG3555 (MEVGWYRSPFSRVVHLYRNGK; RP10245; GenScript) in CFA (263810; BD Difco). Pertussis toxin (200 ng) from Bordetella pertussis (179B; List Biological Laboratories) in PBS was administered i.p. After induction of EAE, mice were observed daily for weight loss, disability, and availability of food and water. …

    Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

Intraneural injection of ATP stimulates regeneration of primary sensory axons in the spinal cord

Wu, D;Lee, S;Luo, J;Xia, H;Gushchina, S;Richardson, PM;Yeh, J;Krgel, U;Franke, H;Zhang, Y;Bo, X;

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

MicroRNA-146a Alleviates Experimental Autoimmune Anterior Uveitis in the Eyes of Lewis Rats

Hsu, Y;Chang, S;Lin, Y;Yang, C;

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

Product: Anti-Cholera Toxin B Subunit (Goat)

Role of Nuclear Factor (Erythroid-Derived 2)-Like 2 Signaling for Effects of Fumaric Acid Esters on Dendritic Cells

Hammer, A;Waschbisch, A;Knippertz, I;Zinser, E;Berg, J;Jrg, S;Kuhbandner, K;David, C;Pi, J;Bayas, A;Lee, DH;Haghikia, A;Gold, R;Steinkasserer, A;Linker, RA;

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

Redox Regulation Mechanisms in Inflammatory Macrophages

Diotallevi, M;

Product: LPS from Escherichia coli O55:B5

  • Chemicals and Kits:

    Lipopolysaccharide from Eschericha coli 055:B5 List Biological Labs, Incorporated

    Spin trapping coupled to EPR:
     
    … This technique was used in this project to evaluate the ROS species release from cells after stimulation by LPS, and if this environment was modified by treatment with BSO. BMPO (5-tert-butoxycarbonyl 5-methyl-1-pyrroline N-oxide) was used as a spin trap. It specifically reacts with O2.-  forming a superoxide adduct, BMPO-OOH, or with HO. forming the hydroxyl adduct, BMPO-OH which is characterised by a 4 lines absorbance spectrum (Figure 2.2). …

    Cell preparation:

    RAW Cells were plated at 5x106cells in 5ml of RPMI media supplemented with 10%FCS and 1%P/S into 25cm2 flasks. At 70% confluence, 120M of BSO, an inhibitor of the synthesis of GSH, was added to the culture for overnight incubation. The next day, cells were stimulated for 2h with LPS. In total four experimental conditions were tested: control, LPS, BSO, BSO+LPS.  

    NOTE:  At the time this paper was written, Product #203 (5mg – LPS from Escherichia coli O55:B5) was utilized.

    Product #203 (5 mg – LPS from Escherichia coli O55:B5) is no longer sold.

    Product #203A (2.5 mg – LPS from Escherichia coli O55:B5) is available for purchase.

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