Zobrazeno 1 - 10
of 88
pro vyhledávání: '"A, Deggerdal"'
Publikováno v:
BioTechniques, Vol 26, Iss 5, Pp 980-983 (1999)
The quality of sequencing results is to a large extent determined by the purity of the template and the purification of the sequencing products. Fragments that can act as unspecific primers and templates are removed before gel analysis, and the backg
Externí odkaz:
https://doaj.org/article/5f0aa533201645ecb4b46f16e2c4ac4b
Publikováno v:
BioTechniques, Vol 22, Iss 3, Pp 506-511 (1997)
A magnetic bead-based system for DNA isolation utilizing monodisperse beads was tested with the aim of producing a general approach for PCR-ready DNA. This commercially available system was originally designed for isolating PCR-ready DNA from human w
Externí odkaz:
https://doaj.org/article/31468c5439e44647b8c37886bb206f49
Autor:
Arne Deggerdal, Frank Larsen
Publikováno v:
BioTechniques, Vol 22, Iss 3, Pp 554-557 (1997)
PCR-based methods for the analysis of genomic DNA are becoming increasingly common both in research and for routine purposes. A rapid, small-scale DNA isolation method is needed to take full advantage of the speed and automation potential of the PCR
Externí odkaz:
https://doaj.org/article/9af585902461485cb9781e88ee2ba928
Autor:
W. B. Gundersen, A. Deggerdal
Publikováno v:
Hereditas. 103:17-22
A strain of Bacillus subtilis, Mu8u5ul, has been used as the recipient in genetic transformation by DNA isolated from two different Bacillus licheniformis strains. Among the markers scored were five antibiotic resistance markers, all located to indis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::517d06838d9f5c5fc922a67c3d767381
https://doi.org/10.1111/j.1601-5223.1985.tb00478.x
https://doi.org/10.1111/j.1601-5223.1985.tb00478.x
Publikováno v:
BioTechniques. 22:506-511
A magnetic bead-based system for DNA isolation utilizing monodisperse beads was tested with the aim of producing a general approach for PCR-ready DNA. This commercially available system was originally designed for isolating PCR-ready DNA from human w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53ba0e0d28145fd7fd71721a447df81e
https://doi.org/10.2144/97223rr01
https://doi.org/10.2144/97223rr01
Autor:
Frank Larsen, Arne Helge Deggerdal
Publikováno v:
BioTechniques. 22:554-557
PCR-based methods for the analysis of genomic DNA are becoming increasingly common both in research and for routine purposes. A rapid, small-scale DNA isolation method is needed to take full advantage of the speed and automation potential of the PCR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::503ad56626820b277bf0fd79b72d3a22
https://doi.org/10.2144/97223pf02
https://doi.org/10.2144/97223pf02
Publikováno v:
Nucleic Acids Research. 22:959-964
In human cells at least 20 different proteins or groups of proteins have been identified that are associated with hnRNAs. These proteins (designated A1-U) are highly abundant in the nucleus. In this study, we present the sequence of a novel cDNA clon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ccca4e1ac679475cb9f42624c62ccaf
https://doi.org/10.1093/nar/22.6.959
https://doi.org/10.1093/nar/22.6.959
Autor:
Arne Deggerdal, Erlend B. Smeland, Heidi Kiil Blomhoff, Cecilia Skjønsberg, Kristin B. Andersson
Publikováno v:
Journal of Cellular Physiology. 157:61-69
The Reh cell system is suitable for evaluating events important for control of proliferation independently of mechanisms involved in differentiation, as Reh cells are unable to differentiate. In the human pre-B cell line Reh, activation of adenylate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14b956d7028a0f1d71ec9f95c115f530
https://doi.org/10.1002/jcp.1041570108
https://doi.org/10.1002/jcp.1041570108
Autor:
Erlend B. Smeland, Dordi Anne Aas-Eng, Arne Deggerdal, Hans Christian Aasheim, Heidi Kiil Blomhoff, Steinar Funderud
Publikováno v:
European Journal of Biochemistry. 213:467-475
In humans, two cDNAs have been isolated encoding beta-galactoside alpha 2,6-sialyltransferase, differing only in part of the 5' untranslated region. Primer extension data show that the two cDNAs are near full-length clones. RNase protection analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d319751d72fe82acb319fc89b7c33eee
https://doi.org/10.1111/j.1432-1033.1993.tb17783.x
https://doi.org/10.1111/j.1432-1033.1993.tb17783.x