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Cpg 2006

Manufactured by Merck Group

CpG 2006 is a synthetic DNA oligonucleotide that acts as a toll-like receptor 9 (TLR9) agonist. It is designed to stimulate the immune system by activating TLR9, which is expressed on certain immune cells. The core function of CpG 2006 is to serve as a research tool for investigating immune system responses and potential therapeutic applications.

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3 protocols using cpg 2006

1

Human B Cell Functional Analysis

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PBMCs were labeled with mAbs against CD20, CD10, CD27, and IgG, and sorted for naïve, transitional, CD27, or unswitched (IgG) memory B cells using the FACSAria III (Becton Dickinson), ensuring >98% purity of the recovered populations. Transitional, naïve, or unswitched memory B cells were cultured in 96-well round-bottom plates (30–40 × 103 cells per well for CFSE analysis or 5 × 103 cells per well to determine Ig secretion). B cells were stimulated with 200 ng/ml CD40L cross-linked to 50 ng/ml HA Peptide mAb (R&D Systems) alone or together with 50 ng/ml IL-21 (PeproTech), 1 μg/ml CpG 2006 (Sigma-Aldrich), 0.05% heat-killed, or formalin-fixed Staphylococcus aureus Cowan I strain (SAC; Sigma-Aldrich). Varying doses of the PI3K p110δ-specific inhibitor leniolisib (Hoegenauer et al., 2017 (link); Rao et al., 2017 (link)) and equivalent doses of DMSO were also added.
B cell viability was determined using the Zombie Aqua Viability dye (BioLegend) and proliferation was measured by CFSE (eBioscience) as described previously (Avery et al., 2010 (link); Hodgkin et al., 1996 (link)). Secretion of IgM, IgG, and IgA by in vitro cultured human transitional, naïve, and memory B cells was determined using Ig heavy-chain specific ELISAs, as described previously (Avery et al., 2005 (link)).
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2

Transitional and Naive B Cell Culture

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PBMCs were labeled with mAbs against CD20, CD27, and CD10 and transitional (CD20+CD10+CD27) or naive (CD20+CD10CD27) B cells were then sorted using a FACSAria III (Becton Dickinson; Cuss et al., 2006 (link); Suryani et al., 2010 (link)). Purity of the recovered populations was >98%. Transitional and naive B cells were then cultured in 96-well U-bottom plates (Falcon; 20–40 × 103/200 µl well) for 4–5 d to determine proliferation and gene expression by qPCR and microarray analysis, or 5 × 103/200 µl well for 5–7 d to determine Ig secretion. B cells were stimulated with 200 ng/ml CD40L cross-linked to 50 ng/ml HA Peptide mAb (R&D Systems) alone or together with 100 U/ml IL-4, 100 U/ml IL-10 (provided by R. de Waal Malefyt, DNAX Research Institute, Palo Alto, CA), 50 ng/ml IL-21 (PeproTech), 2.5 µg/ml F(ab’)2 fragment of goat anti-IgA/IgG/IgM (H+L; Jackson ImmunoResearch), 1 µg/ml CpG 2006 (Sigma-Aldrich), and varying doses of the PI3K p110δ specific inhibitor leniolisib (Hoegenauer et al., 2017 (link); Rao et al., 2017 (link); Novartis Pharma), and equivalent doses of DMSO.
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3

Chemical Compound Procurement for Research

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Ganciclovir (GCV), MG132, CPG 2006, cycloheximide and emetine dihydrochloride hydrate were purchased from Sigma-Aldrich (St. Louis, MO).
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