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      產品中心您現在的位置:首頁 > 產品展示 > > 天然免疫研究產品 > ODN 2216

      ODN 2216

      更新時間:2022-01-28

      簡要描述:

      CpG oligonucleotides (ODNs) are synthetic ODNs that contain unmethylated CpG dinucleotides in particular sequence contexts (CpG motifs).These CpG motifs are present at a 20-fold greater frequency in……

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      Class A CpG oligonucleotide - Human TLR9 ligand

      CpG oligonucleotides (ODNs) are synthetic ODNs that contain unmethylated CpG dinucleotides in particular sequence contexts (CpG motifs).

      These CpG motifs are present at a 20-fold greater frequency in bacterial DNA compared to mammalian DNA. CpG ODNs activate Toll-like receptor 9 (TLR9), leading to strong immunostimulatory effects.

      ODN 2216 is a Class-A CpG ODN that preferentially binds to human TLR9.

      Class A CpG ODNs are characterized by a phosphodiester central CpG-containing palindromic motif and a phosphorothioate 3’ poly-G string.

      They induce high IFN-α production in plasmacytoid dendritic cells (pDC) but are weak stimulators of TLR9-dependent NF-κB signaling.


      Specifications

      Specificity: human TLR9 agonist.

      Working concentration: 1-5 µM.

      Solubility:  5 mg/ml in water.

      ODN 2216 sequence:
      5’-ggGGGACGA:TCGTCgggggg-3’ (20 mer).
      Note: Bases shown in capital letters are phosphodiester, and those in lower case are phosphorothioate (nuclease resistant). Palindrome is underlined.

      Quality control:

      • TLR9 activity has been tested using HEK-Blue™ TLR9 cells.

      • The absence of bacterial contamination (e.g. lipoproteins and endotoxins) has been confirmed using HEK-Blue™ TLR2 and HEK-Blue™ TLR4 cells.


      Contents

      ODN 2216 is provided lyophilized and is available in three quantities.

      tlrl-2216 (formerly tlrl-hodna):

      • 200 μg (31 nmol) lyophilized ODN 2216

      • 1.5 ml sterile endotoxin-free water

      tlrl-2216-1 (formerly tlrl-hodna-1):

      • 1 mg (155 nmol) lyophilized ODN 2216

      • 1.5 ml sterile endotoxin-free water

      tlrl-2216-5 (formerly tlrl-hodna-5):

      • 5 mg (777 nmol) lyophilized ODN 2216

      • 10 ml sterile endotoxin-free water

       

       ODN 2216 is shipped at room temperature.

       Upon receipt, store at -20?°C.


      Description

      CpG ODNs are synthetic oligonucleotides that contain unmethylated CpG dinucleotides in particular sequence contexts (CpG motifs) [1]. These CpG motifs are present at a 20-fold greater frequency in bacterial DNA compared to mammalian DNA. CpG ODNs are recognized by Toll-like receptor 9 (TLR9) leading to strong immunostimulatory effects [2].

      Three types of stimulatory CpG ODNs have been identified, types A, B and C, which differ in their immune-stimulatory activities [3-4]. Type A CpG ODNs are characterized by a phosphodiester central CpG-containing palindromic motif and a phosphorothioate 3’ poly-G string. They induce high IFN-α production from plasmacytoid dendritic cells (pDC) but are weak stimulators of TLR9-dependent NF-κB signaling. Type B CpG ODNs contain a full phosphorothioate backbone with one or more CpG dinucleotides. They strongly activate B cells but stimulate weakly IFN-α secretion. Type C CpG ODNs combine features of both types A and B. They contain a complete phosphorothioate backbone and a CpG-containing palindromic motif. Type C CpG ODNs induce strong IFN-α production from pDC and B cell stimulation.

      ODN 2216 is a CpG ODN type A with a preference for human TLR9.

      1. Krieg, A.M. et al., 1995. CpG motifs in bacterial DNA trigger direct B-cell activation. Nature, 374(6522):546-9.
      2. Bauer, S. et al., 2001. Human TLR9 confers responsiveness to bacterial DNA via species-specific CpG motif recognition. PNAS. 98(16):9237-42.
      3. Krug A. et al., 2001. Identification of CpG oligonucleotide sequences with high induction of IFN- alpha/beta in plasmacytoid dendritic cells. Eur J Immunol, 31(7): 2154-63.
      4. Marshall JD. et al., 2005. Superior activity of the type C class of ISS in vitro and in vivo across multiple species. DNA Cell Biol. 24(2):63-72.


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