Alkaline Lysis Solution I, Plasmid Extraction, 50 mM Glucose, 25 mM Tris, 10 mM EDTA
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Alkaline Lysis Solution I, Plasmid Extraction, 50 mM Glucose, 25 mM Tris, 10 mM EDTA

Cat.No: ATR-SDS-0012 Datasheet

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Product Name Alkaline Lysis Solution I, Plasmid Extraction, 50 mM Glucose, 25 mM Tris, 10 mM EDTA
Catalog No. ATR-SDS-0012
Description The resuspension buffer (Solution I) of the classic alkaline lysis plasmid miniprep protocol, containing glucose for osmotic stabilization, Tris for pH buffering, and EDTA for divalent cation chelation.
Intended Use Resuspension of pelleted bacterial cells as the first step in alkaline lysis plasmid DNA purification prior to addition of SDS-NaOH lysis solution.
Principle / Technology Glucose maintains osmotic pressure to prevent premature cell lysis; Tris maintains pH 8.0 ensuring EDTA chelation of Mg2+ ions; EDTA destabilizes the outer membrane and inhibits endogenous nucleases.
Detection Method Plasmid yield and purity by spectrophotometry, restriction enzyme digest verification, agarose gel analysis
Sample Type Escherichia coli bacterial pellets from overnight culture
Performance Range / Specifications Typical plasmid yield 20–50 µg per 5 mL overnight culture (high-copy plasmid)
Sensitivity / LOD N/A
Specificity N/A
Reaction Conditions / Protocol Resuspend bacterial pellet in 250 µL (per 5 mL culture) by vortexing or pipetting; proceed immediately to Solution II addition.
Components / Formulation Glucose 50 mM, Tris-HCl pH 8.0 25 mM, EDTA 10 mM, RNase A 100 µg/mL (optional)
Storage Conditions 2–8°C (when RNase added); 15–30°C (without RNase)
Shelf Life 6 months (with RNase); 24 months (without RNase)
Package Specifications 100 mL, 500 mL
Product Form Liquid, ready to use
Quality Control pH, osmolality, DNase/RNase free, plasmid extraction efficiency validation
Key Features Ready to use; RNase A pre-added option; standard alkaline lysis component; validated for high and low copy plasmids

For research use only, not for clinical use.

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