Skip to Content
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
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Formaldehyde solution, for molecular biology, 36.5-38% in H2O
Sigma-Aldrich
Protease Inhibitor Cocktail, for plant cell and tissue extracts, DMSO solution
Sigma-Aldrich
Propidium iodide, ≥94.0% (HPLC)
Sigma-Aldrich
Spermidine, ≥99% (GC)
Sigma-Aldrich
Magnesium chloride, anhydrous, ≥98%
Millipore
Triton X-100 Detergent, Molecular Biology Grade, Non-ionic detergent and emulsifier. Has an optimal pH range of 6.0-8.0.
Roche
cOmplete, Mini, EDTA-free Protease Inhibitor Cocktail, Protease Inhibitor Cocktail Tablets provided in a glass vial, Tablets provided in a glass vial