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Merck
  • Isolation of Nuclei in Tagged Cell Types (INTACT), RNA Extraction and Ribosomal RNA Degradation to Prepare Material for RNA-Seq.

Isolation of Nuclei in Tagged Cell Types (INTACT), RNA Extraction and Ribosomal RNA Degradation to Prepare Material for RNA-Seq.

Bio-protocol (2018-04-05)
Mauricio A Reynoso, Germain C Pauluzzi, Sean Cabanlit, Joel Velasco, Jérémie Bazin, Roger Deal, Siobhan Brady, Neelima Sinha, Julia Bailey-Serres, Kaisa Kajala
摘要

Gene expression is dynamically regulated on many levels, including chromatin accessibility and transcription. In order to study these nuclear regulatory events, we describe our method to purify nuclei with Isolation of Nuclei in TAgged Cell Types (INTACT). As nuclear RNA is low in polyadenylated transcripts and conventional pulldown methods would not capture non-polyadenylated pre-mRNA, we also present our method to remove ribosomal RNA from the total nuclear RNA in preparation for nuclear RNA-Seq.

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不含EDTA的cOmplete Mini蛋白酶抑制剂混合物, Protease Inhibitor Cocktail Tablets provided in a glass vial, Tablets provided in a glass vial
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氯化镁, anhydrous, ≥98%
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碘化丙啶, ≥94.0% (HPLC)
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精脒, ≥99% (GC)
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Protease Inhibitor Cocktail, for plant cell and tissue extracts, DMSO solution
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TritonX-100洗涤剂,分子生物学级, Non-ionic detergent and emulsifier. Has an optimal pH range of 6.0-8.0.