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EXTRACTME PLASMID MAXI ENDOTOXIN-FREE KIT

EXTRACTME PLASMID MAXI ENDOTOXIN-FREE KIT
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The EXTRACTME PLASMID MAXI ENDOTOXIN-FREE kit is designed for the efficient purification of high quality plasmid DNA from 200-1000 ml of cultured Escherichia coli cells. The kit is based on modified anion-exchange resin, allowing extraction of ultrapure, transfection-grade pDNA, which is highly suited for use in demanding applications.
Endotoxins <0.1 EU/μg verified by LAL.
 
SAMPLE MATERIAL
Bacterial broth culture:
- 200-600 ml (high-copy number plasmids)
- 400-1000 ml (medium- and low-copy number plasmids)
YIELD
1-1.5 g of transfection-grade pDNA from 400 ml of cultured bacterial cells
TIME REQUIRED
- 120 min
- additional ~60 min for DNA precipitation
DNA PURITY
A260/A280 ratio = 1,7 - 1,9
 
ENDOTOXIN REMOVAL
<0.1 EU/μg verified by LAL
 
Principle
The plasmid DNA purification procedure utilizes pre-packed anion-exchange resin columns which efficiently and selectively bind nucleic acids. In the first isolation step, the pDNA is released from bacterial cells by alkaline lysis. Then the lysate is neutralized and all the cell residues along with the proteins and genomic DNA are separated in the centrifugation step. This alkaline lysis method and RNase treatment are used to obtain clear cell lysate with minimal genomic DNA/RNA contaminants. In the next step the lysate is applied to the purification column with the equilibrated resin and the DNA is bound. The washing stage effectively removes impurities and enzyme inhibitors. A suitable buffer with a high ionic strength allows the elution of the plasmid DNA, which is then concentrated and desalted by precipitation. The purified plasmid DNA may be used directly in all downstream applications such as PCR, qPCR, transfection, microinjection, Southern blotting, DNA sequencing, enzymatic restriction and so forth, or stored until ready to use.
 
Quality control
The quality of each production batch (LOT) of the EXTRACTME PLASMID MAXI ENDOTOXIN-FREE kits is tested using BLIRT’s ISO-certified quality management system. The purified DNA concentration, quality and stability are evaluated by gel electrophoresis and spectrophotometry. In addition, the functional quality is tested by qPCR, digestion with restriction enzymes and pDNA transfection.
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