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ODN 21595
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
CAS NO:1964506-28-2
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
ODN 21595 是一种鸟嘌呤修饰的抑制性寡核苷酸 (INH-ODN)。ODN 21595 抑制 IFN-α 和 IL-6 的释放且无细胞毒性。ODN 21595 降低 CD86 和 HLA-DR 的表达。ODN 21595 具有研究系统性红斑狼疮 (SLE) 的潜力。
生物活性

ODN 21595 is a Guanine-ModifiedTLR7andTLR9inhibitor. ODN 21595 inhibits the release of IFN-α andIL-6with no cytotoxic. ODN 21595 reduces the expression of CD86 and HLA-DR. ODN 21595 has the potential for the research of systemic lupus erythematosus (SLE)[1].

体外研究
(In Vitro)

ODN 21595 (0.01, 0.1, 1, 10 μM; 24 h) inhibits the release of IFN-α in CpG-ODN 2216 (3 μM) and TLR7-ligand RNA-ORN 22075 (5 μM) stimulated human PBMCs[1].
ODN 21595 (0.01, 0.1, 1, 10 μM; 48 h) inhibits the secretion of IL-6 in CpG-ODN 2006 (100 nM) and imiquimod (5 μg/ml) stimulated human PBMCs[1].
ODN 21595 (0.1, 1, 10 μM; 24 h) inhibits the secretion of IL-6 in CpG-ODN 2006 (100 nM) and imiquimod (5 μg/ml) stimulated human B-cells[1].
ODN 21595 (1, 10 μM; 48 h) displays a lower stimulatory activity and reduces significantly the CpG-ODN 2006 (100 nM) or imiquimod (5 μg/ml)-induced expression of CD86 or HLA-DR in CD20+B-cells[1].

Cell Cytotoxicity Assay[1]

Cell Line:human PBMCs
Concentration:0.01, 0.1, 1, 10 μM
Incubation Time:48 h
Result:Showed no cytotoxic for human PBMCs.
CAS 号

1964506-28-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.