RNA immunoprecipitation technique for Drosophila melanogaster S2 cells
- Авторы: Kachaev Z.M.1, Gilmutdinov R.A.1, Kopytova D.V.1, Zheludkevich A.A.1, Shidlovskii Y.V.1, Kurbidaeva A.S.1
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Учреждения:
- Institute of Gene Biology
- Выпуск: Том 51, № 1 (2017)
- Страницы: 72-79
- Раздел: Molecular Cell Biology
- URL: https://journal-vniispk.ru/0026-8933/article/view/162933
- DOI: https://doi.org/10.1134/S002689331606008X
- ID: 162933
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Аннотация
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.
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Об авторах
Z. Kachaev
Institute of Gene Biology
Автор, ответственный за переписку.
Email: k-z-m@mail.ru
Россия, Moscow, 119334
R. Gilmutdinov
Institute of Gene Biology
Email: k-z-m@mail.ru
Россия, Moscow, 119334
D. Kopytova
Institute of Gene Biology
Email: k-z-m@mail.ru
Россия, Moscow, 119334
A. Zheludkevich
Institute of Gene Biology
Email: k-z-m@mail.ru
Россия, Moscow, 119334
Y. Shidlovskii
Institute of Gene Biology
Email: k-z-m@mail.ru
Россия, Moscow, 119334
A. Kurbidaeva
Institute of Gene Biology
Email: k-z-m@mail.ru
Россия, Moscow, 119334
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