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文献和实验Analysis of Protein-DNA Binding by Streptavidin-Agarose Pulldown
. We describe here a streptavidin-agarose pulldown assay that is capable of analyzing quantitatively binding of an array of proteins to DNA probes. The assay is easy to perform and does not require radiolabeled probes. It involves incubation of nuclear extract proteins
Purification of DNA‐Binding Proteins Using Biotin/Streptavidin Affinity Systems
by adsorption onto a biotin?containing resin. Since streptavidin is multivalent, it is able to serve as a bridge between the biotinylated DNA fragment and the biotin?containing resin. Proteins remaining in the supernatant are removed by washing, and the resin
Extraction of DNA from Agarose Gels
, to destabilize the agarose gel. The DNA is subsequently bound to a substrate (e.g., an anionic resin) and washed to remove impurities prior to elution of the DNA from the substrate. Other methods include hot phenol extraction of the DNA from the gel. The use
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