1983
DOI: 10.1016/s0022-2836(83)80190-9
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Lambda replacement vectors carrying polylinker sequences

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Cited by 1,709 publications
(616 citation statements)
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“…Fragments of 14-24 kb were enriched by centrifugation through a sucrose density gradient and used to construct a genomic library in EMBL3 h cloning vector as described [12].…”
Section: Methodsmentioning
confidence: 99%
“…Fragments of 14-24 kb were enriched by centrifugation through a sucrose density gradient and used to construct a genomic library in EMBL3 h cloning vector as described [12].…”
Section: Methodsmentioning
confidence: 99%
“…Two genomie libraries from human kidney and brain tissue in lambda EMBL-4 phages were constructed by the method of Frischauf [6]. 2,3 x 106 phages were screened by hybridization with the eDNA of CSAP [5] which was labeled before with ~2p by random priming using a kit from Pharmacia (Freiburg, Germany).…”
Section: Isolation Of Genomic Clonesmentioning
confidence: 99%
“…Escherichia coli strains DH5a [6] and XL1-Blue (Stratagene) were the host strains for the plasraids pUC9 [7] and pBluescript (Stratagene), respectively. E. coil strains NM 538 and NM 539 were host strains for propagation of phage A EMBL3 and its derivatives [8]. Bacterial cells were grown in LB media under the appropriate selective conditions [9].…”
Section: Strains and Culture Conditionsmentioning
confidence: 99%
“…Then about 80 ng Aspergillus DNA fragments were ligated to 500 ng vector arms. After in vitro packaging, recombinant phages were selected according to their ability to grow in cells of E. coli NM 539 carrying prophage P2 [8].…”
Section: Isolation Of Chromosomal Dna and Construction Of A Genomic Lmentioning
confidence: 99%