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ODN 1668 sodium

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Catalog No. T212714

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’.

ODN 1668 sodium

ODN 1668 sodium

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Catalog No. T212714
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’.
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Product Introduction

Bioactivity
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.
Chemical Properties
Storage & Solubility Information
StorageLyophilized powder: -20~-80°C for 1 year

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent 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.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
% DMSO
%
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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