RNA immunoprecipitation technique for Drosophila melanogaster S2 cells
- 作者: Kachaev Z.M.1, Gilmutdinov R.A.1, Kopytova D.V.1, Zheludkevich A.A.1, Shidlovskii Y.V.1, Kurbidaeva A.S.1
-
隶属关系:
- Institute of Gene Biology
- 期: 卷 51, 编号 1 (2017)
- 页面: 72-79
- 栏目: Molecular Cell Biology
- URL: https://journal-vniispk.ru/0026-8933/article/view/162933
- DOI: https://doi.org/10.1134/S002689331606008X
- ID: 162933
如何引用文章
详细
RNA-binding proteins play an important role in RNA metabolism, especially in mRNA biogenesis and subsequent expression patterns regulation. RNA immunoprecipitation (RIP) is a powerful tool for detecting protein–RNA associations. In this paper, we briefly cover the history of this method for analyzing RNA–protein interactions and reviewing a number of modifications of the RIP technique. We also present an adjusted RIP protocol that was modified for Drosophila S2 cell culture. The use of this protocol allows one to perform the efficient precipitation of RNA–protein complexes and harvest RNA in amounts that are sufficient for its downstream analysis.
作者简介
Z. Kachaev
Institute of Gene Biology
编辑信件的主要联系方式.
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
R. Gilmutdinov
Institute of Gene Biology
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
D. Kopytova
Institute of Gene Biology
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
A. Zheludkevich
Institute of Gene Biology
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
Y. Shidlovskii
Institute of Gene Biology
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
A. Kurbidaeva
Institute of Gene Biology
Email: k-z-m@mail.ru
俄罗斯联邦, Moscow, 119334
补充文件
