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Chromatographic purification and separation of plasmid and lambda phage DNAs

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F02%3A00006665" target="_blank" >RIV/00216224:14310/02:00006665 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Chromatographic purification and separation of plasmid and lambda phage DNAs

  • Original language description

    Plasmid pBR322 DNA was purified by gel permeation chromatography. Recovered plasmid DNA was free of RNA and retained its biological activity. The biological activity of purified plasmid DNA was tested by electrotransformation into bacterial cells. DNA fragments of lambda DNA and lambda DNA were separated on column for gel permeation chromatography. Small fragments were eluted in void volume; large fragments and lambda DNA were separated in reversed order than expected according to GPC and according to the slalom chromatography mechanisms.

  • Czech name

    Chromatographic purification and separation of plasmid and lambda phage DNAs

  • Czech description

    Plasmid pBR322 DNA was purified by gel permeation chromatography. Recovered plasmid DNA was free of RNA and retained its biological activity. The biological activity of purified plasmid DNA was tested by electrotransformation into bacterial cells. DNA fragments of lambda DNA and lambda DNA were separated on column for gel permeation chromatography. Small fragments were eluted in void volume; large fragments and lambda DNA were separated in reversed order than expected according to GPC and according to the slalom chromatography mechanisms.

Classification

  • Type

    D - Article in proceedings

  • CEP classification

    EI - Biotechnology and bionics

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA203%2F00%2F1339" target="_blank" >GA203/00/1339: Dispersion polymerisation of hydrophilic monomers for the preparation of magnetic carriers used in biotechnological application</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2002

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    22nd International Symposium on the Separation of Proteins, Peptides and Polynucleotides

  • ISBN

  • ISSN

  • e-ISSN

  • Number of pages

    1

  • Pages from-to

    53-53

  • Publisher name

    Dechema

  • Place of publication

    Heidelberg, Germany

  • Event location

    November, 10-13, 2002, Heidelberg, Germany

  • Event date

    Jan 1, 2002

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article