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HOME > Product search results > Code No. RN1007 BRIC Kit

Code No. RN1007


Availability (in Japan)


(In Japan at 17:00,
Apr 19, 2021 in JST)


20 assays


  • BrU-labeled RNA was isolated by BRIC Kit from total RNA extracted after BrU pulse-chase labeling.

  • BrU-labeled RNA (BrU-RNA) was isolated by BRIC Kit from total RNA extracted at each time point after BrU washout. The isolated BrU-RNA was analyzed to determine its own half-life by RT-qPCR.

Components RNA-IP buffer, Wash buffer, mi-Solution I, mi-Solution II, mi-Solution III, mi-Solution IV, Protein G-Magnetic beads, BrU solution (100 mM), Anti-BrdU mAb, Spike-in control
Intended use The BRIC Kit is designed to analyze stability of RNA by chasing chronological decreases of BrU-labeled RNA in mammalian cells under physiologically undisturbed condition.
Storage temp. -20°C Manufacturer MBL
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  1. Ueno D et al. Comprehensive analysis of mRNA internal cleavage sites in Arabidopsis thaliana. J Biol Bioeng. (2018) In press.(PMID:29358038)
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  3. Imamachi N et al. BRIC-seq: a genome-wide approach for determining RNA stability in mammalian cells. Methods 67, 55-63 (2014)(PMID: 23872059
  4. Tani H et al. The RNA degradation pathway regulates the function of GAS5 a non-coding RNA in mammalian cells. PLoS One 8, e55684 (2013)(PMID: 23383264
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Product category
Research area
RNA-RNP Network
RiboCluster Profiler™

  • The availability is based on the information in Japan at 17:00, Apr 19, 2021 in JST.
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  • For storage temparature: RT: room temparature
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