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- 详细信息
- 文献和实验
- 技术资料
- 保质期:
/
- 英文名:
ODN 2395
- 库存:
大量
- 供应商:
Neobioscience
- CAS号:
/
- 保存条件:
-20
- 规格:
1 mg
货号:tlrl-2395-1
规格:1 mg
产品描述:
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 effects2 . Three classes of stimulatory CpG ODNs have been identified, classes A, B and C, which differ in their immunostimulatory activities3-4. 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-a production from plasmacytoid dendritic cells (pDC) but are weak stimulators of TLR9-dependent NF-kB 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-a secretion. Class C CpG ODNs combine features of both classes A and B. They contain a complete phosphorothioate backbone and a CpGcontaining palindromic motif. Class C CpG ODNs induce strong IFN-a production from pDC and B cell stimulation. ODN 2395 is a Class C CpG ODN with a preference for human and murine TLR9.
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文献和实验Antisense Efficacy: Site-Restricted In Vivo and Ex Vivo Models
In the laboratory, antisense oligodeoxynucleotides (ODN) have repeatedly demonstrated efficacy in modulating the expression of various genes, thus providing important insights into their roles in tumorigenesis or normal growth and development
Modulation of human interferon- biosynthesis by antisense oligodeoxynucleotides
We investigated the inhibition of human interferon-γ (HuIFN-γ) production in cultures of lymphocytes with the use of the antisense strategy. Out of a series of antisense oligodeoxynucleotides (ODN) complementary to different regions of the HuIFN
Transport of Antisense Across the Blood-Brain Barrier
. Recently, two types of unmodified antisense analogs have been shown to effectively cross the BBB and affect CNS function. One of the analogs, a phosphorothioate oligodeoxy-nucleotide (P-ODN) directed against the amyloid β protein, was peripherally
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