Northern blot
A technique for separating RNA molecules by electrophoresis and then identifying a target fragment with a DNA probe.
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A technique for separating RNA molecules by electrophoresis and then identifying a target fragment with a DNA probe.
An immunologic technique for the detection of specific messenger RNAs using complementary DNA. Called also Northern transfer.
The northern blot is a technique used in molecular biology research to study gene expression. It takes its name from the similarity of the procedure to the Southern blot procedure, named for biologist Edwin Southern, used to study DNA, with the key difference that, in the northern blot, RNA, rather than DNA, is the substance being analyzed by electrophoresis and detection with a hybridization probe. This technique was developed in 1977 by James Alwine, Kemp, and George Stark at Stanford University.[1]
The gels may be run on either agarose or denaturing polyacrylamide gels depending on the size of the RNA to be detected. A notable difference in the procedure in case of agarose gels, (as compared with the Southern blot) is the addition of formaldehyde which acts as a denaturant. For smaller fragments denaturing polyacrylamide urea gels are employed.
As in the Southern blot, the hybridization probe may be made from DNA or RNA.
A variant of the procedure known as the reverse northern blot was occasionally (although, infrequently) used. In this procedure, the substrate nucleic acid (that is affixed to the membrane) is a collection of isolated DNA fragments, and the probe is RNA extracted from a tissue and radioactively labelled.
The use of
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Southern blot (DNA) - Western blot (protein) - Northern blot (RNA) - Southwestern blot (protein:DNA) - Far-western blotting (protein:protein) |
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