Related Experiment Video

Updated: Aug 21, 2026

DNA Stable-Isotope Probing (DNA-SIP)
14:57

DNA Stable-Isotope Probing (DNA-SIP)

Published on: August 2, 2010

Size fractionation of double-stranded DNA by precipitation with polyethylene glycol

J T Lis, R Schleif

    Nucleic Acids Research
    |March 1, 1975
    PubMed

    More Related Videos

    Iterative Optimization of DNA Duplexes for Crystallization of SeqA-DNA Complexes11:42

    Iterative Optimization of DNA Duplexes for Crystallization of SeqA-DNA Complexes

    Published on: November 1, 2012

    Preparation of DNA-crosslinked Polyacrylamide Hydrogels09:06

    Preparation of DNA-crosslinked Polyacrylamide Hydrogels

    Published on: August 27, 2014

    Related Concept Videos

    DNA Isolation01:34

    DNA Isolation

    DNA from cells is required for many biotechnology and research applications, such as molecular cloning. To remove and purify DNA from cells, researchers use various methods of DNA extraction. While the specifics of different protocols may vary, some general concepts underlie the process of DNA extraction.
    DNA Isolation01:24

    DNA Isolation

    DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
    DNA Agarose Gel Electrophoresis02:35

    DNA Agarose Gel Electrophoresis

    Agarose gel electrophoresis is a laboratory technique commonly used to separate DNA fragments by size. However, it can also be used to isolate and purify DNA fragments using a gel extraction protocol.
    Gel extraction follows five major steps: running gel electrophoresis to separate fragments, isolating the individual bands, extracting DNA from those bands, and removing the dye and salts from the extracted mixture to obtain pure DNA.
    In cloning experiments, both the insert and vector DNA...
    SDS-PAGE01:27

    SDS-PAGE

    Gel electrophoresis is a method that separates biological macromolecules like nucleic acids or proteins by forcing them to pass through a gel matrix under an electric field.
    A variation of gel electrophoresis, termed  polyacrylamide gel electrophoresis (PAGE), is commonly used for separating proteins according to their molecular size by passing them through a polyacrylamide gel. Because of the varying charges associated with amino acid side chains, PAGE can be used to separate intact proteins...