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ODN 1668 sodium is a B class CpG ODN (oligodeoxynucleotide) recognized as a TLR-9 agonist. It demonstrates potent immunomodulatory effects by enhancing the level of IgG2 subtype antibodies and stimulating both T cell and B cell immune responses, making it useful for vaccine adjuvant research. Additionally, CpG ODN 1668 sodium induces antibacterial immune responses in orange-spotted grouper through a CaTLR9-dependent pathway. Sequence: 5’-tccatgacgttcctgatgct-3’.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | ODN 1668 sodium is a B class CpG ODN (oligodeoxynucleotide) recognized as a TLR-9 agonist. It demonstrates potent immunomodulatory effects by enhancing the level of IgG2 subtype antibodies and stimulating both T cell and B cell immune responses, making it useful for vaccine adjuvant research. Additionally, CpG ODN 1668 sodium induces antibacterial immune responses in orange-spotted grouper through a CaTLR9-dependent pathway. Sequence: 5’-tccatgacgttcctgatgct-3’. |
| In vitro | ODN 1668, at a non-salt dosage, ranging from 6-60 µg/mL for 12-72 hours, enhances the synthesis of S100A8/A9, IL-6, and β-galactosidase in mouse bone marrow-derived macrophages. Administered for 24 hours, ODN 1668 promotes B cell activation and proliferation while increasing the expression of CD86 and CD25. Additionally, ODN 1668, at concentrations of 0.3-3.0 μM over four days, supports the dose-dependent growth of CD8+ T cells treated with anti-CD3. At concentrations from 0.25-32 μg/mL for 12 hours, ODN 1668 promotes head kidney lymphocyte proliferation and enhances the expression of immune-related genes. |
| In vivo | Non-salt dosage: ODN 1668 (10 nmol ≈ 63.6 μg; injected into the hind paw; single dose) significantly enhanced the antibody response and increased IgG2a and IgG2b titers in OVA-treated mice. ODN 1668 (15 μg; intramuscular injection; single dose) improved the grouper's antimicrobial immunity against delayed cestode infection, with the liver, spleen, and kidneys showing the most pronounced antibacterial activity. ODN 1668 (1-5 mg/kg; intraperitoneal/subcutaneous injection; single dose) can induce fever, anorexia, and brain inflammation in rats. |
| Storage | Lyophilized powder: -20~-80°C for 1 year |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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