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Fluorescence in situ hybridization with rRNA-targeted oligonucleotide probes Jakob Pernthaler1×, FrankOveralll ckner1, Wilhelm Sch nhuber2, Rudolf Amann1 1 Max-Planck-Institute for Marine Microbiology,
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How to fill out fluorescence in situ hybridization:

01
Prepare the sample by fixing cells or tissues onto a slide.
02
Denature the DNA or RNA in the sample to ensure proper hybridization.
03
Apply the fluorescently labeled probes that are specific to the target DNA or RNA sequence.
04
Incubate the sample to allow the probes to hybridize with the target sequences.
05
Wash away any unbound probes.
06
Mount the slide and examine it under a fluorescence microscope to visualize the hybridized probes.

Who needs fluorescence in situ hybridization:

01
Researchers and scientists working in genetics and molecular biology often use fluorescence in situ hybridization to study gene expression, chromosome abnormalities, and genomic variations.
02
Fluorescence in situ hybridization is commonly used in clinical settings for diagnostic purposes, such as detecting specific genetic abnormalities or determining the presence of certain pathogens.
03
This technique is also employed in the fields of pathology and oncology to aid in the diagnosis and monitoring of various diseases, including cancer.
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Fluorescence in situ hybridization (FISH) is a molecular cytogenetic technique used to detect and localize the presence or absence of specific DNA sequences on chromosomes.
Researchers and medical professionals who need to analyze specific DNA sequences on chromosomes are required to perform fluorescence in situ hybridization.
Fluorescence in situ hybridization is performed by preparing a sample with specific DNA probes, hybridizing the probes to the chromosomes, and then visualizing the results using fluorescence microscopy.
The purpose of fluorescence in situ hybridization is to identify and locate specific DNA sequences on chromosomes, which can be helpful in genetic research, diagnosis of genetic disorders, and monitoring disease progression.
Fluorescence in situ hybridization reports typically include details on the specific DNA probes used, the chromosome location of the DNA sequences, and any abnormalities or mutations detected.
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