Isolating RNA from tissues and paraffin-embedded tissue samples can be challenging due to cross-linking of biomolecules and fragmented nucleic acids. The best solution is to slice the tissues into smaller pieces and make a homogenate solution (using tissue homogenizer or grinding liquid nitrogen frozen samples) in presence of RNAse inhibitors. The homogenization process should be carried out on dry ice to maintain the integrity of RNA.
Isolating RNA from tissues and paraffin-embedded tissue samples can be challenging due to cross-linking of biomolecules and fragmented nucleic acids. The best solution is to slice the tissues into smaller pieces and make a homogenate solution (using tissue homogenizer or grinding liquid nitrogen frozen samples) in presence of RNAse inhibitors. The homogenization process should be carried out on dry ice to maintain the integrity of RNA.
Get tips on using TRIzol™ Plus RNA Purification Kit to perform RNA isolation / purification Cells - primary rabbit aortic endothelial cells
Get tips on using NEBNext® Ultra™ Directional RNA Library Prep Kit for Illumina® to perform RNA sequencing Mouse - RAW264.7
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized 293T
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized VCaP
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized U87
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized T98G
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized PNT2
Get tips on using RNAzol® RT to perform RNA isolation / purification Cells - immortalized LNCaP
Fill out your contact details and receive price quotes in your Inbox
Outsource experiment