2008
DOI: 10.1080/00218839.2008.11101432
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Comparison of microsatellite DNA diversity among commercial queen breeder stocks of Italian honey bees in the United States and Italy

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Cited by 13 publications
(11 citation statements)
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“…This may be an artifact of marker selection. The markers selected for this study differ from those used in previous studies assessing genetic diversity for both Russian and Italian honey bees (Bourgeois et al 2008, Bourgeois andRinderer 2009). The markers in the current study were selected for homogeneity within each grouping (i.e., Russian or non-Russian).…”
Section: Discussionmentioning
confidence: 99%
“…This may be an artifact of marker selection. The markers selected for this study differ from those used in previous studies assessing genetic diversity for both Russian and Italian honey bees (Bourgeois et al 2008, Bourgeois andRinderer 2009). The markers in the current study were selected for homogeneity within each grouping (i.e., Russian or non-Russian).…”
Section: Discussionmentioning
confidence: 99%
“…It is known that the anion products of dissolved salts individually affect the aggregation or precipitation of proteins from solutions such that the efficacies can be described by the Hofmeister series (Zhang & Cremer, ; Kunz, ). Although many DNA extraction protocols (Bourgeois et al., , ; Bourgeois & Rinderer, ) and kits use acetate salts (potassium or ammonium), we chose to focus on sodium chloride due to its availability and universal use in a variety of laboratories. Chloride anion is considered a marginally functional salting‐out factor, somewhat less effective than acetate on the Hofmeister series.…”
Section: Resultsmentioning
confidence: 99%
“…Traditional phenol‐chloroform extractions require handling, storage, and disposal of hazardous organic solvents. Honey bee DNA has recently been effectively extracted and purified by homogenization and utilizing proteinase K and ‘salting‐out’ methods to remove proteins (Bourgeois et al., , ; Bourgeois & Rinderer, ). However, we developed a simple, cost‐effective, and fast method using only sodium chloride and sodium dodecylsulfate (SDS) to extract clean DNA directly useable for PCR without additional dilution as is typically required.…”
Section: Introductionmentioning
confidence: 99%
“…Queens of one group can be produced and mated simultaneously. This mating scheme has resulted in a stock that retains good genetic diversity among groups and lines (Bourgeois et al, 2008). Also, allelic frequency differences at molecular loci enable RHBs to be distinguished from other commercial stocks with very high accuracy (Bourgeois and Rinderer, 2009).…”
Section: Development Of a Closed Breeding Population Of Rhbmentioning
confidence: 99%