1997
DOI: 10.5962/bhl.title.143318
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Use of "Lysis Buffer" in DNA isolation and its implication for museum collections

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Cited by 329 publications
(320 citation statements)
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“…We collected contour feathers and blood samples by venipunction of the brachial vein (~40 μl). Samples were stored separately in test tubes containing 95 % ethanol (feathers) or Longmire buffer (Longmire et al 1997;blood sample), and preserved at -20 °C until analyzed. Partridges were released within 30 min in the same capture site.…”
Section: Methodsmentioning
confidence: 99%
“…We collected contour feathers and blood samples by venipunction of the brachial vein (~40 μl). Samples were stored separately in test tubes containing 95 % ethanol (feathers) or Longmire buffer (Longmire et al 1997;blood sample), and preserved at -20 °C until analyzed. Partridges were released within 30 min in the same capture site.…”
Section: Methodsmentioning
confidence: 99%
“…We extracted genomic DNA from skeletal muscle or organ tissue samples with standard phenol methods (Longmire et al, 1997). We followed Van Den Bussche and Hoofers (2000) methods to amplify and sequence a 2.6 kilobase-fragment of mtDNA encompassing 12S rRNA, tRNA Val , and 16S rRNA genes.…”
Section: Molecular Methodsmentioning
confidence: 99%
“…and deposited in the Mammalogy Division of Museo de Zoología at the Pontificia Universidad Católica del Ecuador, Quito, Ecuador (QCAZ 8478). Tissues (heart, kidney and liver) were preserved in lysis buffer (Longmire et al 1997) and deposited at the Angelo State Natural History Collection, Angelo State University, San Angelo, Texas, USA (ASK 7645).…”
mentioning
confidence: 99%