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Pierce Cell Lysis Reagents  |
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Bacterial protein extraction reagents (B-PER) for efficient yet gentle extraction of proteins, especially recombinant proteins, from E. coli and other bacteria. Several convenient formulations available.
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A special guanidine-hydrochloride solution to effectively solubilize purified inclusion bodies.
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An optimized insect cell protein extraction reagent (I-PER).
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The most effective reagent method for preparing protein extracts from plant tissues.
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The Pierce IP Lysis Buffer is a moderate strength lysis buffer that effectively solubilizes cytoplasmic, membrane and nuclear proteins but does not liberate genomic DNA or disrupt protein complexes like RIPA buffer.
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A high-quality prepared form of the traditional RIPA lysis buffer for routine cell lysis and protein extraction.
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A gentle ready-to-use cell lysis solution for cultured mammalian cells that requires no scraping, freeze-thaw cycles or sonication!
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A mild detergent-based lysis buffer for extracting proteins from soft mammalian tissues.
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A special formulation of yeast protein extraction reagent that uses a dialyzable detergent to facilitate compatibility with downstream applications.
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An effective detergent-based lysis buffer for protein extraction from yeast cells.
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DNA extraction and purification reagents for Saccharomyces cerevisiae and selected other species of yeast.
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A fast, easy-to-use system for detecting ß-Galactosidase in yeast cells. The homogenous assay procedure includes cell lysis solution and detection reagents.
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Enzyme for digesting single and double-stranded DNA in molecular biology applications and to aid in cell lysis for protein extraction.
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An enzyme that facilitates cell lysis and protein extraction when added to detergent-based reagents.
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A cell lysis reagent for prokaryotic and eukaryotic cells that facilitates the release of DNA in a form ready for PCR.
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A fast, easy-to-use system for measuring ß-Galactosidase activity in mammalian cells.
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D-Luciferin is primarily used in reporter assays and ATP assays. Our D-Luciferin is specially purified by a chiral-specific HPLC method to ensure maximum activity.
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