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Detection of Caprine-specific Nucleic Acid Sequences in Goat Milk Using Polymerase Chain Reaction

Bibliographic Data

ID22320585
AuthorsAsim Osman (0000-0002-3163-7114, National Ribat University), Imadeldin E Aradaib (0000-0002-9335-0848, University of Khartoum), Imadeldin Aradaib, Omer Musa, Omer Said Musa (University of Khartoum)
Year2013
Volume25
Issue2
Pages105
Publication date2013-01-01
Open AccessYes
TypeARTICLE
VenueMateria Socio Medica (JOURNAL)
Journal identifiersISSN: 1512-7680 • E-ISSN: 1986-597X
PublisherScopeMed (PUBLISHER • TR)
DOI10.5455/msm.2013.25.105-108
PMID24493993
OpenAlexW2160436832
LanguageEN

CONFLICT OF INTEREST: none declared. INTRODUCTION: This study was carried out to evaluate PCR-based method for detection of DNA in goat milk. It utilized primers targeting the mitochondrial cytochrome -b (mtcyt-b) gene, which was used as a target DNA for PCR amplification. METHODS: For the specific identification of goat mtcyt-b gene, pair of primers (GSL1, GSR2), were used, which produced a 428 base pair (bp) PCR product from milk samples as well as from peripheral blood. Amplification products were visualized on ethidium bromide-stained agarose gels. RESULTS AND DISCUSSION: Amplification products were not detected when the PCR was applied to DNA from animal species including cattle, sheep, swine, camel, deer, horse, donkey, and human, which indicates that the 2 pairs of primers are specific for goat. CONCLUSION: DNA can be extracted from goat milk and would be advantageous in the variety of application such as species identification in milk and milk

Biology · DNA · Donkey · Ethidium bromide · Gene · Mitochondrial DNA · Nucleic acid · Polymerase chain reaction · Real-time polymerase chain reaction · Animal Diversity and Health Studies · Identification and Quantification in Food · Milk Quality and Mastitis in Dairy Cows · Genetics · Molecular Biology

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