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- Cossarizza, A., et al.
(författare)
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Guidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
- 2019
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Ingår i: European Journal of Immunology. - : Wiley. - 0014-2980 .- 1521-4141. ; 49:10, s. 1457-1973
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Tidskriftsartikel (refereegranskat)abstract
- These guidelines are a consensus work of a considerable number of members of the immunology and flow cytometry community. They provide the theory and key practical aspects of flow cytometry enabling immunologists to avoid the common errors that often undermine immunological data. Notably, there are comprehensive sections of all major immune cell types with helpful Tables detailing phenotypes in murine and human cells. The latest flow cytometry techniques and applications are also described, featuring examples of the data that can be generated and, importantly, how the data can be analysed. Furthermore, there are sections detailing tips, tricks and pitfalls to avoid, all written and peer-reviewed by leading experts in the field, making this an essential research companion.
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| 2. |
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| 3. |
- Ghaani, M., et al.
(författare)
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Determination of 2,4-diaminotoluene by a bionanocomposite modified glassy carbon electrode
- 2018
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Ingår i: Sensors and actuators. B, Chemical. - : Elsevier B.V.. - 0925-4005 .- 1873-3077. ; 277, s. 477-483
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Tidskriftsartikel (refereegranskat)abstract
- This work describes the development of a modified glassy carbon electrode (GCE) for the selective determination of 2,4-diaminotoluene (TDA), a primary aromatic amines (PAAs) that can be formed in food packaging materials including aromatic polyurethane (PU) adhesives. The electrode's surface was modified with multi-walled carbon nanotubes (MWCNTs), MWCNTs in chitosan (CS), and gold nanoparticles (AuNPs). The highest current response was achieved with AuNPs/MWCNTs-CS/GC electrodes, which exhibited an oxidation peak of 9.87 μA by cyclic voltammetry (CV), compared with 1.39 μA of the bare GCE. A detection limit of 35 nM was estimated by amperometry experiments. The oxidation of TDA was strongly dependent on the pH of the medium, having maximum sensitivity at pH ∼ 7. From a mechanistic point of view, the diffusion coefficient of TDA (D = 6.47 × 10−4 cm2 s−1) and the number of electrons (n ≈ 2) involved in the catalytic oxidation of TDA at the surface of the AuNPs/MWCNTs-CS/GCE were determined. The practical utility of this nanocomposite modified electrode was demonstrated by migration studies from conventional food packaging materials.
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| 4. |
- Merluzzi, S, et al.
(författare)
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CD40 stimulation induces Pax5/BSAP and EBF activation through a APE/ref-1-dependent redox mechanism
- 2004
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Ingår i: Journal of Biological Chemistry. - : American Society for Biochemistry and Molecular Biology. - 0021-9258 .- 1083-351X. ; 279:3, s. 1777-1786
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Tidskriftsartikel (refereegranskat)abstract
- CD40 is a member of the growing tumor necrosis factor receptor family that has been shown to play important roles in T cell-mediated B lymphocyte activation. Ligation of B cell CD40 by CD154, mainly expressed on activated T cells, stimulates B cell proliferation, differentiation, isotype switching, up-regulation of surface molecules contributing to antigen presentation, development of the germinal center, and the humoral memory response. In this study we demonstrate that the redox factor APE/Ref-1 acts as a key signaling intermediate in response to CD40-mediated B cell activation. The transcription factors Pax5a or BSAP ( B cell lineage-specific activator protein) and EBF ( early B cell factor) are constitutively expressed in spleen B cells and CD40 cross-linking induces increases in Pax5a and EBF binding activity compared with nonstimulated B cells. We show that upon CD40 antibody-mediated cross-linking, APE/Ref-1 translocates from the cytoplasm to the nucleus of activated B cells, where it modulates the DNA binding activity of both Pax5a and EBF. Moreover, we show that the repression of APE/Ref-1 protein production is able to block CD40-mediated Pax5a activation. We also provide evidence that APE/Ref-1 can modulate the cooperative activation of the blk promoter operated by Pax5a and EBF and that APE/Ref-1 might directly regulate EBF functional activity. Finally, we show that the interaction between Pax5a and EBF enhances EBF binding activity to its consensus sequence, suggesting that Pax5a can physically interact with EBF and modulate its DNA binding activity.
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