Abstract
We herein describe a procedure that allows for simultaneous genotyping of six loss-of-function mutations in the bovine myostatin gene associated with the double-muscling phenotype. The proposed method relies on a multiplex oligonucleotide ligation assay and detection of the fluorescently labelled products using automatic sequencers.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Base Sequence
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Cattle / genetics*
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DNA Primers
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Genetic Techniques*
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Muscle Development*
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Muscles / metabolism
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Mutation*
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Myostatin
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Oligonucleotides
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Transforming Growth Factor beta / genetics*
Substances
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DNA Primers
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Myostatin
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Oligonucleotides
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Transforming Growth Factor beta