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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
A5207 DNA Ladder 1 kb 50 ¥ìg / 250 ¥ìg • 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
A5194 DNA Marker Phage Lambda - Sty I 50 ¥ìg • 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
A5193 DNA Isolation Spin-Kit Agarose 50 Isolations Kit for the DNA isolation from agarose gels with spin minicolumns • Application of the DNA in cloning and sequencing • performance of the electrophoresis in either TAE or TBE buffer • Binding capacity of the columns 10 ¥ìg • Isolation of DNA fragments in the range of 100 to 6000 bp
A5191 DNA Ladder 100 bp 50 ¥ìg / 250 ¥ìg • Fragment sizes in bp: 1000; 900; 800; 700; 600; 500 (x2); 400; 300; 200; 100 • Number of bands: 10 Concentration: 0.2 mg/mL
A5187 DNA Phage Lambda 1 mg Concentration: 0.2 - 0.5 mg/mL
A5076 Magnesium Chloride 25 mmol/l (25 mM) for molecular biology 5 ml DNases/RNases/Proteases: not detectable Concentration: 25 mM Composition: MgCl2 ¡¤ 6H2O: 5.08 g/L
A4051 TRItidy G¢â 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
A3660 DNA Ladder Mix 100 - 5000 (lyophilised) 50 ¥ìg • Number of bands: 17 • Fragment sizes in bp: 5000; 4000; 3000; 2500; 2000; 1500; 1000; 900; 800; 700; 600; 500 (x2); 400; 300; 200; 150; 100 • supplied with loading buffer (1X) • recommended loadings: 0.5 - 0.8 ¥ìg/lane • extremely stable: storage for at least 4 years at -20¡ÆC possible
A3640 Bromophenol Blue Sodium Salt for electrophoresis 34725-61-6 5 g CAS No. 34725-61-6 / Solid / M.W 691.94 g/mol

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