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- Biolegend
- 155102
- 2025年11月24日
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文献和实验Purification of Recombinant Poly(ADP-Ribose) Polymerases
extract are separated on a Heparine Sepharose™ column. The PARP-containing fractions are then affinity purified on a 3-aminobenzamide Sepharose™ chromatographic step. The last contaminants and the 3-methoxybenzamide used to elute the PARP from the previous
Expression and Preparation of Fusion Proteins from Recombinant gt1.1 Phages
-level expression, the relative stability of β-galactosidase fusion proteins, and simple approaches to purify the fusion proteins. After the desired clone is detected and purified, it is often necessary to obtain preparative amounts of recombinant protein
Quantifying In Vivo Somatic Mutations Using Transgenic Mouse Model Systems
Mouse, lacZ in the MutaMouse, and the gpt delta assay. Briefly, high-molecular-weight DNA is purified from the tissue of interest and used as substrate during in vitro packaging reactions, in which the λ transgenes are excised from the genome
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