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miRNA Sponge Clone miRNA sponge technology was first introduced by Sharp’s laboratory in 2007 as a means to generate RNA molecules containing multiple, tandem binding sites for a miRNA seed family of interest and able to block a whole family of related miRNAs. This method is a useful tool for study of miRNA loss-of-function. miRNAs in a same family often share a common seed sequence (positions of 2–8 of the miRNA, the major specificity determinant for target recognition). The sponge mRNA contains multiple target sites complementary to a miRNA of interest. When the sponge vector is transfected into cells and the sponge mRNA is expressed at high levels, it specifically inhibits the activity of a family of miRNAs sharing a common seed. RGBiotech offers high quality service for construction of miRNA sponge vector clones to assist researchers worldwide on their miRNA studies. Features & Benefits Tabel 1. Comparison of miRNA sponge and antagomir
References [1]. EbertMS, Neilson JR, Sharp PA: MicroRNA sponges: Competitive inhibitors of small RNAs in mammalian cells. Nat Methods 2007, 4:721–726.[2]. Ebert MS, Sharp PA: MicroRNA sponges: progress and possibilities. RNA 2010, 16: 2043–2050. >Contact Us For more information about our miRNA services, please contact us at admin@rgbiotech.com. |
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