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Soluble anti cd28 37

Manufactured by Thermo Fisher Scientific

Soluble anti-CD28 (37.51) is a laboratory reagent used in cell culture and immunological research. It functions as an activator of the CD28 co-stimulatory receptor, which plays a crucial role in T-cell activation and proliferation. This product is provided in a soluble format for convenient addition to cell culture systems.

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2 protocols using soluble anti cd28 37

1

T Cell Activation and Stimulation Protocol

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Human CD4+ T cells purified from peripheral blood mononuclear cells (PBMCs) using EasySepTM human CD4+ T cell enrichment kit (StemCell Technologies, Vancouver, Canada) were stimulated with plate-bound anti-CD3ε (OKT3, eBioscience, San Diego, CA) plus soluble anti-CD28 (CD28.2 eBioscience, San Diego, CA). Procedures with human subjects were approved by the Institutional Review Board of the University of California, Irvine and were conducted in conformity with the 1954 Declaration of Helsinki in its currently applicable version. Similarly, mouse T cells were stimulated with plate-bound anti-CD3ε (2C11, eBioscience, San Diego, CA) plus soluble anti-CD28 (37.51, eBioscience, San Diego, CA). Mgat5 wild-type and heterozygous mice were used for mouse experiments and approved by the Institutional Animal Care and Use Committee of the University of California, Irvine. Both human and mouse cells were cultured in RPMI 1640 medium, supplemented with 10% fetal bovine serum, 2 mM L-glutamine, 100 units/ml penicillin, and 100 ug/ml streptomycin, and 50 μM β-mercaptoethanol. GlcNAc was obtained from Wellesley Therapeutics Inc. (Toronto, Canada) while all acetylated forms of GlcNAc were obtained from Santa Cruz Biotechnology (Dallas, TX). GlcNAc and its acetylated forms were >95% pure.
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2

In vitro Treg Differentiation Assay

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CD4+CD25 T cells (106/ml) were pre-incubated with 1 uM ODN for 2 h and then transferred to a 96 well plate coated with 3 ug/ml anti-CD3 (2C11; eBioscience, San Diego, CA). Cells were cultured in complete medium (RPMI 1640 supplemented with 10% FCS (both from Lonza, Walkersville, MD), 2 mM glutamine, 100 IU/ml penicillin, 100 ug/ml streptomycin, 25 mM HEPES buffer (all from Invitrogen, Carlsbad, CA), 0.0035% 2 ME (Sigma Aldrich, St. Louis, MO) and stimulated with 2 ug/ml soluble anti-CD28 (37.51; eBioscience) plus 20 ng/ml human TGFb1 (R&D Systems). 20 ng/ml of IL-2 (R&D Systems) was included to support the proliferation of Tregs from C57Bl/6 mice. This supplementation was not needed for T cells from BALB/c mice which intrinsically produce sufficient IL-2 when stimulated [28 (link)]. In experiments examining whether Sup ODN influenced the differentiation of iTreg, only 5 ng of TGFβ1 was added during culture. At the indicated time points, cells were analyzed for FoxP3 expression by flow cytometry or used in functional assays.
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