1978
DOI: 10.1016/0003-2697(78)90262-2
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The isolation of high molecular weight DNA from whole organisms or large tissue masses

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Cited by 169 publications
(63 citation statements)
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“…Samples from the field were placed, separately, into 1.5 ml vials containing 240 µl lysis buffer (Graham 1978), homogenized, and extracted with 240 µl phenol/chloroform. The material was shipped to the laboratory in Israel, where DNA isolation was completed by additional phenol/chloroform and chloroform extraction.…”
Section: Methodsmentioning
confidence: 99%
“…Samples from the field were placed, separately, into 1.5 ml vials containing 240 µl lysis buffer (Graham 1978), homogenized, and extracted with 240 µl phenol/chloroform. The material was shipped to the laboratory in Israel, where DNA isolation was completed by additional phenol/chloroform and chloroform extraction.…”
Section: Methodsmentioning
confidence: 99%
“…DNA extraction and microsatellite typing of colonies were performed as per . Samples from the field were placed separately into vials containing lysis buffer (Graham 1978), homogenized and extracted with phenol/chloroform. Five Botryllus schlosseri microsatellites, BS-811 (Pancer et al 1994), PB-29, PB-41, PB-49 and PBC-1 (Stoner et al 1997), were used following primers and suggested conditions.…”
Section: Samplingmentioning
confidence: 99%
“…Tissue was broken and DNA extracted as described by Graham (1978). DNA was further purified according to the UP procedure described by Britten etal.…”
Section: Methodsmentioning
confidence: 99%