The principle of FISH involves the use of fluorescently labeled DNA probes that bind to complementary sequences of DNA within the cell. These probes are designed to target specific regions of the genome, allowing researchers to visualize the location of these sequences within the cell.
Procedure
Preparation of the sample: The sample, such as cells or tissue sections, is fixed to glass slides to preserve the cellular structure.
Denaturation: The DNA in the sample is denatured to separate the double-stranded DNA into single strands.
Hybridization: The fluorescently labeled DNA probes are added to the sample and allowed to hybridize with the complementary DNA sequences.
Washing: The unbound probes are washed away to remove non-specific binding.
Visualization: The sample is examined under a fluorescence microscope to visualize the fluorescently labeled DNA probes and their location within the cell.
Cellular biology: Understanding the structure and organization of cells, particularly the nucleus and its components, is important for visualizing the localization of DNA sequences using FISH.
Applications: Familiarize yourself with the various applications of FISH in genetics, clinical diagnostics, and research to understand its significance in the field of biology.
By mastering these fundamental concepts, you will be well-prepared to understand and apply the principles of fluorescence in situ hybridization in various biological contexts.
Identify and analyze forces responsible for changes in rotational motion and develop an understanding of the effect of rotational inertia on the motion of a rotating object (e.g., merry-go-round, spinning toy, spinning figure skater, stellar collapse [supernova], rapidly spinning pulsar).