RNA is then separated by chloroform and precipitated with isopropanol. The RNA sample, from leaf tissue, for example, is homogenized using guanidium isothiocyanate and phenol which disrupts cells and inactivates RNases. The first method involves organic solvents like phenol and chloroform to extract RNA. Two methods can be used to extract RNA from cells or tissues: The initial and crucial step in the Northern blot technique is RNA extraction, which determines the quality and quantity of the RNA molecule being analyzed. Let’s take a closer look at the Northern blotting steps in detail. This enables researchers to detect the RNA molecule by autoradiography or other detection methods. The gel is then transferred to a membrane, such as nitrocellulose or nylon, where RNA is immobilized.įollowing the transfer, RNA is hybridized with a DNA or RNA probe whose sequence complements the target RNA molecule. The Northern blotting technique involves separating RNA molecules based on their size by agarose gel electrophoresis (transcript size >=1kb) or polyacrylamide gel electrophoresis (transcript size < 1kb). General steps in a Northern blotting experiment While Southern blot analyzes DNA, Northern blot analyzes RNA. This technique, developed in 1977, is similar to Southern blot, but it analyzes different nucleic acids. And in addition to detecting the quantity of specific transcripts, Northern blot also helps determine the sizes of specific transcripts under investigation. This method is useful for monitoring the transcription and transcript abundance of a target gene in a cell or tissue sample by assaying for the corresponding RNA.īy measuring the transcript levels of your gene of interest, you can monitor the tissue-wide expression pattern of your gene as well as how its transcript is turned over. Northern blot is a molecular biology technique used to detect levels of RNA molecules of a specific sequence in your sample.
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