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Daniel J. Simpson

Researcher at Promega

Publications -  22
Citations -  3074

Daniel J. Simpson is an academic researcher from Promega. The author has contributed to research in topics: Nucleic acid & RNA. The author has an hindex of 15, co-authored 22 publications receiving 2674 citations. Previous affiliations of Daniel J. Simpson include Office of Technology Transfer & Woods Hole Oceanographic Institution.

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Journal ArticleDOI

HaloTag: A Novel Protein Labeling Technology for Cell Imaging and Protein Analysis

TL;DR: The utility of this modular protein tagging system for cellular imaging and protein immobilization is demonstrated by analyzing multiple molecular processes associated with NF-kappaB-mediated cellular physiology, including imaging of subcellular protein translocation and capture of protein--protein and protein--DNA complexes.
Journal ArticleDOI

Evidence for anoxygenic photosynthesis from the distribution of bacteriochlorophylls in the Black Sea.

TL;DR: It is suggested that anoxygenic photosyn-thesis is a relatively recent phenomenon in the Black Sea initiated by shallowing of the chemocline over the past decade and develop-ment of an anoxic layer devoid of O2 and H2S (ref. 7).
Journal ArticleDOI

Luminogenic cytochrome P450 assays.

TL;DR: Luminogenic cytochrome P450 (CYP) assays couple CYP enzyme activity to firefly luciferase luminescence in a technology called P450-GloTM (Promega) to offer advantages of speed and safety over HPLC and radiochemical-based methods.
Journal ArticleDOI

HaloTag7: a genetically engineered tag that enhances bacterial expression of soluble proteins and improves protein purification.

TL;DR: A novel protein tag engineered to enhance expression and solubility of recombinant proteins and to provide efficient protein purification coupled with tag removal, designed to bind rapidly and covalently with a unique synthetic linker to achieve an essentially irreversible attachment.
Patent

pH dependent ion exchange matrix and method of use in the isolation of nucleic acids

TL;DR: In this article, the pH dependent ion exchange matrices are designed to bind to the target nucleic acid at a pH wherein the overall charge of the matrix is positive, and to release as the pH of the surrounding solution is increased.