2006
DOI: 10.1016/j.forsciint.2005.08.007
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Identification of animal species by protein radioimmunoassay of bone fragments and bloodstained stone tools

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Cited by 41 publications
(22 citation statements)
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“…Several alternative approaches to species identification of fragmentary bones have been considered, ranging from histology (Hars anyi 1993;Hillier & Bell 2007;Cuijpers & Lauwerier 2008;Greenlee & Dunnell 2010), to biomolecular analyses (Lowenstein et al 2006;Blow et al 2008). Histological analysis, which can be considered a type of morphological analysis on a microscopic scale, is relatively low cost but has not been adopted widely in archaeology or palaeontology due to the amount of time, expense and technical expertise required in relation to the limited taxonomic resolution available (Cuijpers 2006).…”
mentioning
confidence: 99%
“…Several alternative approaches to species identification of fragmentary bones have been considered, ranging from histology (Hars anyi 1993;Hillier & Bell 2007;Cuijpers & Lauwerier 2008;Greenlee & Dunnell 2010), to biomolecular analyses (Lowenstein et al 2006;Blow et al 2008). Histological analysis, which can be considered a type of morphological analysis on a microscopic scale, is relatively low cost but has not been adopted widely in archaeology or palaeontology due to the amount of time, expense and technical expertise required in relation to the limited taxonomic resolution available (Cuijpers 2006).…”
mentioning
confidence: 99%
“…Highest percentage of binding reflects a significant reaction and is interpreted as an identification of a species. Non-identification (''no reaction'') occurs when values are extremely low; we consider significant reactions to be !3 (following earlier studies, e.g., Lowenstein et al, 2006). Weak reactions can occur when one of the three test runs yields significant high binding values and subsequent testing yields little to no reaction values.…”
Section: Pria Techniquementioning
confidence: 70%
“…The protein-based methods rely on immune assays or chromatography that includes gas chromatography (GC) [6], liquid chromatography (LC) [25], high-performance liquid chromatography (HPLC) [5], enzyme-linked immunosorbent assay (ELISA) [26], several blotting immunological assays [27,28], and electrophoretic analysis [29,30]. However, each technique has its own limitations, such as being expensive, laborious, inadequate, and time-consuming, diverse range of equipment, and difficulty to the interpretation of obtained results [10].…”
Section: Introductionmentioning
confidence: 99%