Hybridization probe

From WikiMD's Food, Medicine & Wellness Encyclopedia

Hybridization probe is a fragment of DNA or RNA molecule used in molecular biology to detect the presence of nucleotide sequences (the target) that are complementary to the sequence in the probe. The probe binds through base pairing, also known as hybridization, to the target sequence and marks it for detection.

Overview[edit | edit source]

Hybridization probes are used in many different applications in molecular biology, including gene expression studies, genotyping, mutation detection, and genomic mapping. They are also used in clinical diagnostics for the detection of specific pathogens or genetic disorders.

Design and Synthesis[edit | edit source]

The design of a hybridization probe depends on the specific application. In general, the probe is designed to be complementary to a specific target sequence. The probe is usually synthesized chemically, but it can also be produced by PCR or cloning.

The length of the probe can vary, but it is typically between 20 and 50 nucleotides. The probe is often labeled with a radioactive or fluorescent marker to allow detection.

Hybridization[edit | edit source]

The process of hybridization involves the binding of the probe to the target sequence. This is usually done in a solution containing the target DNA or RNA. The solution is heated to denature the target, separating the two strands. The probe is then added, and the solution is cooled to allow the probe to bind to the target.

Detection[edit | edit source]

After hybridization, the probe-target complex can be detected using various methods. If the probe is labeled with a radioactive marker, the complex can be detected using autoradiography. If the probe is labeled with a fluorescent marker, the complex can be detected using fluorescence microscopy or flow cytometry.

Applications[edit | edit source]

Hybridization probes are used in a wide range of applications in molecular biology and clinical diagnostics. They are used in gene expression studies to detect specific mRNAs, in genotyping to detect specific alleles, and in mutation detection to identify specific genetic changes. They are also used in genomic mapping to locate specific sequences on chromosomes.

In clinical diagnostics, hybridization probes are used to detect specific pathogens, such as viruses or bacteria, or to detect specific genetic disorders.

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