Andrew C. Chen, achen@spa.ars.usda.gov, USDA-ARS, KBUSLIRL, 2700 Fredericksburg Road, Kerrville, TX and Kevin B. Temeyer, Kevin.Temeyer@ars.usda.gov, USDA-ARS-KBUSLIRL, 2700 Fredericksburg Rd, Kerrville, TX.
Single nucleotide polymorphism (SNP) genotyping has been carried out by various methods, including differential hybridization such as allele-specific oligonucleotide hybridization and fluorescent probes (molecular beacon, TaqMan); melting temperature-based analyses such as single-stranded conformational polymorphism (SSCP), heteroduplex analysis, DHPLC and fluorescence melting curves; allele-specific amplification; and DNA sequencing or primer extension to distinguish alleles. All these methods are either cumbersome to perform or expensive in both the equipment and reagents required. We have developed a method based on fluorescence-labeled allele specific probes. The alleles can be simply visually distinguished on agarose gel after amplification of genomic DNA.
Species 1: Acari Ixodidae
Boophilus microplus (southern cattle tick)
Keywords: SNP, fluorescence
Poster (.pdf format, 83.0 kb)