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24. Explain what a DNA probe is and how it could be used to identify a person who carries an allele for a genetic disorder.

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Step-by-step explanation:

DNA probes are stretches of single-stranded DNA used to detect the presence of complementary nucleic acid sequences (target sequences) by hybridization. DNA probes are usually labelled, for example with radioisotopes, epitopes, biotin or fluorophores to enable their detection.

Laboratory tests, including genetic testing: Molecular, chromosomal, and biochemical genetic or genomic testing are used to diagnose genetic disorders. Other laboratory tests that measure the levels of certain substances in blood and urine can also help suggest a diagnosis.

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