Endotoxin-Free Plasmid DNA Mini Extraction Kit
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Endotoxin-Free Plasmid DNA Mini Extraction Kit

Cat.No: DREK-0091 Datasheet

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Product Name Endotoxin-Free Plasmid DNA Mini Extraction Kit
Catalog No. DREK-0091
Description A spin-column kit for rapid purification of high-yield plasmid DNA with low endotoxin carryover. The workflow combines alkaline lysis, selective silica-membrane binding and dedicated impurity removal for transfection-ready DNA.
Intended Use Plasmid DNA purification for restriction digestion, PCR, sequencing, ligation, transformation and cell transfection.
Principle / Technology Optimized alkaline lysis followed by selective silica-membrane adsorption and endotoxin-removal chemistry.
Detection Method Downstream DNA analysis and transfection performance.
Sample Type 1-5 mL overnight bacterial culture.
Performance Range / Specifications Approximately 25-minute workflow; plasmid DNA yield up to 50 µg; endotoxin residue ≤0.1 EU/µg DNA.
Specificity Selective recovery of plasmid DNA while reducing endotoxin, protein, genomic DNA and other bacterial impurities.
Reaction Conditions / Protocol Harvest the bacterial culture, resuspend and lyse the pellet, neutralize and clarify the lysate, bind plasmid DNA to the spin column, wash and elute.
Components / Formulation Alkaline lysis, neutralization, binding, wash and elution reagents with silica spin columns and collection tubes.
Storage Conditions Store at 15-25°C.
Package Specifications 50 reactions.
Product Form Endotoxin-free plasmid DNA spin-column kit.
Quality Control Yield, DNA integrity, purity and endotoxin-removal performance are evaluated during release testing.
Key Features Up to 50 µg yield; endotoxin ≤0.1 EU/µg; approximately 25-minute workflow; no hot-cold phase switching; transfection-compatible DNA.
Shipping Conditions Ship at room temperature.
Compatibility Common mammalian cell transfection and routine molecular biology workflows.
Application Notes / Precautions Use a healthy overnight culture and avoid overloading the column. Handle lysates gently after alkaline lysis to minimize genomic DNA contamination.
Batch-to-Batch Consistency Yield, purity and endotoxin-removal performance are controlled across production batches.

For research use only, not for clinical use.

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