rna-isolation-purification-cells-primary-rat-cardiac-fibroblasts

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Get tips on using NucleoSpin® RNA to perform RNA isolation / purification Tissue - Human Decidua

Products Macherey Nagel NucleoSpin® RNA

Get tips on using NucleoSpin® RNA to perform RNA isolation / purification Tissue - Human Bladder

Products Macherey Nagel NucleoSpin® RNA

Get tips on using NucleoSpin® RNA to perform RNA isolation / purification Tissue - Human Adipose

Products Macherey Nagel NucleoSpin® RNA

Get tips on using illustra RNAspin Mini Kit to perform RNA isolation / purification Cells - immortalized BRL 3A

Products GE Healthcare Life Sciences illustra RNAspin Mini Kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Cells - immortalized BEAS-2B

Products Qiagen miRNeasy Mini kit

Get tips on using miRNeasy Mini kit to perform RNA isolation / purification Cells - immortalized A2780/DDP

Products Qiagen miRNeasy Mini kit

Get tips on using TruSeq RNA Library Prep Kit v2 to perform RNA sequencing Rat - Retinal ganglion cells (RGCs)

Products Illumina TruSeq RNA Library Prep Kit v2

Get tips on using PolyATtract® mRNA Isolation Systems to perform RNA isolation / purification Yeast - Coprinus cinereus

Products Promega PolyATtract® mRNA Isolation Systems

Hello! I used Trizol to extract total RNA from in-vitro cultured bacteria (1 X 10^8 cells). After phase separation, I mixed ~0.4 ml of the upper phase which contains RNA with 0.5 mL cold isopropanol. However, the amount of RNA when measured in Nanodrop was very low. In addition, the ratio between 260 and 230 was around 0.1 to 0.5. Is there a chance that my sample was contaminated by the Trizol reagent? When I collected the aqueous phase I made sure to not touch the lower phase. What should I do?

Discussions Some help with RNA isolation using Trizol

Get tips on using RNeasy Plus Mini Kit to perform RNA isolation / purification Cells - immortalized HeLa, CaSki and C33A (Cervical cancer cells)

Products Qiagen RNeasy Plus Mini Kit

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