Genopure Plasmid Maxi Kit

Description

• General description: For large-scale (maxi) preparation of plasmid DNA.
• Application: The Genopure Plasmid Maxi Kit prepares transfection-grade plasmid DNA in large quantities (up to 500 μg plasmid) from bacterial cultures. Isolated plasmid is suitable for most molecular biology applications:TransfectionSouthern blottingSequencingPCR/long PCRRestriction digestionCloning
• Features and Benefits: The Genopure Plasmid Maxi Kit prepares highly purified plasmid DNA in large quantities using a modified alkaline lysis method.Save time with ready-to-use reagents.Purify up to 10 samples (10 minutes hands-on-time/75 minutes overall).Purify all sizes and types of plasmideven BAC DNA, since the crude lysate can be filtered to avoid plasmid shearing.Process multiple samples in parallelusing high speed gravity-flow columns.Eliminate the use of hazardous organic compoundssuch as cesium chloride, phenol, chloroform, and ethidium bromide.Obtain higher purity plasmid DNAover plasmid prepared by 2 x cesium chloride gradient centrifugation.
• Components: Suspension BufferRNase ALysis BufferNeutralization BufferEquilibration BufferWash BufferElution BufferNucleoBond AX 500 ColumnsFolded Filters (240 mm diameter)Sealing Rings
• Quality: Plasmid DNA purified by this kit has been tested for restriction digestion; pUC 19 was isolated from transformed HB101 as described in the protocol. 1 μg of plasmid was completely digested with 1 U Msp I for 2 hours at +37°C, as shown by agarose gel analysis.Plasmid recovery was tested with 250 μg purified plasmid. The recovery was >90%, with more than 80% in supercoiled form. The yield of plasmid DNA was determined by isolating pBS from DH5a cells. From 150 ml culture volume with a density of A600 between 3 and 6, >400 μg of plasmid DNA was obtained.The purity (checked by the ratio of A260/A280) is 1.8 + 0.2.RNA contamination was analyzed with 3 μg pBS purified with the standard procedure and checked by electrophoresis on an agarose gel. No RNA was detected.The kit components have been tested for the absence of nucleases according to current quality control procedures.
• Preparation Note: The isolation procedure is based on a modified alkaline lysis protocol and can be divided into the following steps:The bacteria are partially lysed, allowing the plasmid DNA to escape the cell wall into the supernatant. The larger E. coli chromosomal DNA is trapped in the cell wall. The lysate is cleared of cellular debris by filtration or centrifugation, and the plasmid DNA-containing fraction is loaded onto a pre-equilibrated column. Since the cleared lysate is applied to the column in a low-salt buffer, plasmid DNA binds to the macroporous anion-exchange material in the column. Cellular impurities are eluted from the column with a high-salt wash. Finally, the plasmid DNA is eluted from the column. Recovered DNA is precipitated from the eluate to remove salt and concentrate the plasmid.
• Analysis Note: Sample:E. coli culture that contains a high-copy number plasmid: 30 to 150 mL bacterial cultureE. coli culture that contains a low-copy number plasmid: 100 to 500 mL bacterial culturePlasmid Size: The isolation procedure is suitable for all sizes of plasmid. Note: Lysates of larger constructs (up to 100 kb) should be cleared by filtration rather than centrifugation to avoid shearing the plasmid.Time Required: 75 minutes (including filtration of the lysate)Typical Yield:High-copy number plasmid: 3 to 5 μg/mL cultureLow-copy number plasmid: 0.2 to 1 μg/mL cultureProduct Purity: Isolated plasmid DNA is free of other bacterial components, including RNA.
• Other Notes: Ion Exchange Chromatography