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In the center of molecular biology is one species of molecules: DNA.
DNA molecules are amplified and introduced into organisms by transformation or transfection, separated, stained, examined under the microscope, manipulated, sequenced and so on.
For all these techniques the initial step is to isolate DNA from the origin of interest.
This page provides you an overview of the different methods for nucleic acid isolation and offers a number of must-have reagents to obtain pure DNA and/or RNA from various sources.

Introduction
What does it mean technically when we talk about DNA extraction, isolation or purification - terms often used synonymously for getting preferably pure DNA from a sample? What are the mechanisms behind? How is it possible to separate distinct species of DNA?
On this page we focus on the isolation of the two DNA species that are mainly isolated in molecular biology labs - genomic DNA and bacterial plasmids. We give an overview about established DNA isolation techniques, their chemical background and we discuss their respective advantages and limitations.

Regarding the basic procedure, DNA extraction is simple and can be done using domestic products. Basically, all you require is a rich source of DNA, salt, water, dishwashing detergent, a coffee filter, high-proof alcohol and a stick to spool the precipitated DNA salt out of solution. For higher demands (regarding quantity and quality), of course, the method requires further refinement.
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Thumbnail Catalog Description Packaging Specification
A5216 DNA Ladder 100 bp plus 50 ¥ìg / 250 ¥ìg • Fragment sizes in bp: 1500; 1000 (x2); 900; 800; 700; 600; 500 (x2); 400; 300; 200; 100 • Number of bands: 11 Concentration: 0.2 mg/mL
A1624 Phenol water-saturated, stabilized 108-95-2 500 ml CAS No. 108-95-2 / Liquid
A5324 Magnesium Chloride solution (100 mM) for molecular biology 1 ml DNases/RNases/Proteases: not detectable Concentration: 100 mM
A1578 Phenol water-saturated, non-stabilized 108-95-2 500 ml CAS No. 108-95-2 / Liquid
A5456 Tetramethylammonium Chloride solution (6 M) for molecular biology 500 ml DNases/RNases/Proteases: not detectable Composition: TMACl: 657 g/L
A1153 Phenol equilibrated, stabilized 108-95-2 100 ml / 250 ml / 500 ml CAS No. 108-95-2 / Liquid
A9801 qPCR Cycler Validation Kit 2 Tests Usage: for real-time/qPCR thermal cyclers with optical unit
A7248 Dimethyl Sulfoxide, sterile filtered (ampules) 67-68-5 5 x 10 ml CAS No. 67-68-5 / Liquid / M.W 78.13 g/mol
A2160 Salmon sperm DNA Sodium Salt 9007-49-2 1 g CAS No. 9007-49-2 / Solid
A9742 PCR Cycler Validation Kit 2 Tests Annealing temp. 63¡ÆC: two amplicons Annealing temp. 65¡ÆC: one amplicon Annealing temp. 68¡ÆC: no amplicon

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