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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
A0871 Formamide ultrapure 75-12-7 1 L CAS No. 75-12-7 / Liquid / M.W 45.04 g/mol
A8511 SYBR Green® staining reagent, DNA free 5 x 0,625 ml / 10 x 0,625 ml Bacterial DNA: not detectable (min. 40 PCR cycles) Concentration: 10X concentrated solution
A5207 DNA Ladder 1 kb 50 μg / 250 μg • Fragment sizes in kb: 10.0, 8.0, 6.0, 5.0, 4.0, 3.0 (x2), 2.5, 2.0, 1.5, 1.0 (x2), 0.75, 0.5, 0.25 • Number of bands: 13 Concentration: 0.2 mg/mL
A4051 TRItidy G™ 100 ml / 200 ml • mono-phasic reagent (contains phenol and guanidinium thiocyanate) • suited for small and large samples • for samples of human, animal, plant and bacterial origin • isolation of intact total RNA from tissue and cells, sequential precipitation of DNA and protein
A3470 DNA Ladder 100 bp (lyophilised) 50 μg • Number of bands: 11 • Fragment sizes in bp: 1000; 900; 800; 700; 600; 500 (x2); 400; 300; 200; 150; 100 • supplied with loading buffer (1X) • recommended loadings: 0.4 - 0.8 μg/lane • extremely stable: storage for at least 4 years at -20°C possible
A1091 Agarose MP 9012-36-6 100 g / 250 g / 500 g CAS No. 9012-36-6 / Solid
A8963 Agarose Basic 9012-36-6 100 g / 250 g / 500 g / 1 kg CAS No. 9012-36-6 / Solid
A5194 DNA Marker Phage Lambda - Sty I 50 μg • Fragment sizes in bp: 19329*; 7743; 6223; 4254*; 3472; 2690; 1882, 1489; 925; 421; 74 • Number of bands: 11 Concentration: 0.2 - 0.5 mg/ml
A3481 Loading buffer DNA IV (for Agarose gels) 10 ml / 25 ml Composition: Bromophenol blue: 0.25 % EDTA · Na2 (pH 8.0): 100 mM Ficoll® 400: 20 % SDS: 1.0 % Xylene cyanol FF: 0.25 %
A9555 DNA-Dye NonTox 1 ml ♦ nonhazardous Ethidium bromide substitute • Loading buffer with highly sensitive DNA dye • contains three tracking dyes • Visualization of DNA with blue light und UV light

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