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      ODN 1826

      更新時(shí)間:2022-01-29

      簡要描述:

      ODN 1826 is a class B CpG ODN specific for murine TLR9.CpG-B ODNs contain a full phosphorothioate backbone with one or more CpG dinucleotides.They strongly activate B cells but weakly stimulate ……

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      Class B CpG oligonucleotide - Murine TLR9 agonist

      ODN 1826 is a class B CpG ODN specific for murine TLR9.

      CpG-B ODNs contain a full phosphorothioate backbone with one or more CpG dinucleotides.

      They strongly activate B cells but weakly stimulate IFN-α secretion in plasmacytoid dendritic cells (pDCs).

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

      A 20-fold higher frequency of these CpG motifs is found in bacterial DNA compared to mammalian DNA.

      CpG ODNs activate Toll-like receptor 9 (TLR9), leading to strong immunostimulatory effects.


      Specifications

      Specificity: Murine TLR9 agonist

      Working concentration: 1-5 µM

      Solubility: 5 mg/ml in water

      ODN 1826 sequence
      5’-tccatgacgttcctgacgtt-3’ (20 mer)
      Note:  This ODN contains a full phosphorothioate backbone and is nuclease resistant.

      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 1826 is provided lyophilized and is available in three quantities:

      tlrl-1826 (formerly tlrl-modn):

      • 200 μg (31.42 nmol) lyophilized ODN 1826

      • 1.5 ml sterile endotoxin-free water

      tlrl-1826-1 (formerly tlrl-modn-1):

      • 1 mg (157.1 nmol) lyophilized ODN 1826

      • 1.5 ml sterile endotoxin-free water

      tlrl-1826-5 (formerly tlrl-modn-5):

      • 5 mg (785.5 nmol) lyophilized ODN 1826

      • 10 ml sterile endotoxin-free water

       

       ODN 1826 is shipped at room temperature.

       Upon receipt it should be stored 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 classes (A, B and C) of stimulatory CpG ODNs have been identified which differ in their immune-stimulatory activities [3-4].
      Class A CpG ODNs are characterized by a phosphodiester central CpG-containing palindromic motif and a phosphorothioate 3’ poly-G stretch. They induce high IFN-α production from plasmacytoid dendritic cells (pDCs) but are weak stimulators of TLR9-dependent NF-κB signaling.
      Class 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.
      Class C CpG ODNs combine features of both types A and B. They contain a complete phosphorothioate backbone and a CpG-containing palindromic motif. Class C CpG ODNs induce strong IFN-a production from pDCs as well as B cell stimulation.

      ODN 1826 is a Class B CpG ODN specific for murine TLR9 [5].

       

      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.
      5. Ballas ZK. et al., 2001. Divergent therapeutic and immunologic effects of oligodeoxynucleotides with distinct CpG motifs. J Immunol. 167(9):4878-86.


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