TOOLS Plasmid Mini kit
TOOLS Plasmid Mini kit is based on alkaline lysis technology followed by adsorption of DNA onto silica membrane in the presence of high salt. Plasmid DNA purified with this product is immediately ready for use. Phenol extraction and ethanol precipitation are not required. High-quality plasmid DNA is eluted in a small volume of Tris Buffer or deionized water. This protocol is designed for purification of up to 30 μg of plasmid DNA (<12kb) from 1-4 ml overnight cultures of E. coli in LB (Luria-Bertani) medium. Plasmid DNA prepared by this kit is suitable for a variety of routine applications including restriction enzyme digestion, sequencing, library screening, ligation and transformation, in vitro translation, and transfection of robust cells.
Features
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High yields of plasmid DNA
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Cost-effective preparations
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For optimum lysis and maximum DNA yield.
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Work Flow
Q1. Purity of plasmid affect the efficiency of restriction enzymes?
A: In fact, there are many factors that affect the activity of enzyme, generally speaking, they are related to temperature, buffer composition, DNA configuration or methylation, sample purity, and, in addition, sample purity, if the sample contains Protein, EDTA, Ethanol, SDS, Chloroform, Phenol, ion, etc., they will also affect the activity of enzyme.
A: In fact, there are many factors that affect the activity of enzyme, generally speaking, they are related to temperature, buffer composition, DNA configuration or methylation, sample purity, and, in addition, sample purity, if the sample contains Protein, EDTA, Ethanol, SDS, Chloroform, Phenol, ion, etc., they will also affect the activity of enzyme.
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HSIEH, Yen‐Che, et al. Pparα deficiency inhibits the proliferation of neuronal and glial precursors in the zebrafish central nervous system. Developmental Dynamics, 2018, 247.12: 1264-1275.