Isolation of genomic DNA from tissues—NucleoBond AXG

Anion exchange columns for purification of ultra-pure genomic DNA from tissue, bacteria, or yeast by gravity flow

NucleoBond AXG columns are anion-exchange columns for isolating ultra-pure genomic DNA from tissue, bacteria, or yeast. Macherey-Nagel offers buffer sets for extracting genomic DNA from tissue and bacteria, which include all required buffers and enzymes (Proteinase K and RNase A). Using these buffer sets in combination with NucleoBond AXG columns allows isolation of up to 500 µg of genomic DNA from different matrices. 

NucleoBond AXG columns are anion-exchange columns for isolating ultra-pure genomic DNA from tissue, bacteria, or yeast. Macherey-Nagel offers buffer sets for extracting genomic DNA from tissue and bacteria, which include all required buffers and enzymes (Proteinase K and RNase A). Using these buffer sets in combination with NucleoBond AXG columns allows isolation of up to 500 µg of genomic DNA from different matrices. Isolation of genomic DNA from yeast requires additional buffers (see user manual). NucleoBond AXG columns are available in three different sizes (AXG 20, AXG 100, and AXG 500).

The quality of the isolated genomic DNA is extraordinarily high. AXG columns used to purify genomic DNA with a gravity flow-based protocol yield high molecular weight DNA without shearing. Samples are first lysed with Proteinase K. Before loading, the sample is diluted with Buffer N2 in order to guarantee a good flow rate as well as quantitative DNA binding. After efficient washing, the genomic DNA is eluted with high-salt buffer and precipitated with isopropanol. The DNA purified using this method is suitable for all kinds of subsequent reactions.

Overview

  • Ultra-pure genomic DNA from from tissue, bacteria, or yeast
  • Combine NucleoBond AXG columns and the corresponding buffer set for highest flexibility
  • NucleoBond AXG columns + NucleoBond Buffer Set III for isolation of genomic DNA from bacteria and yeast
  • NucleoBond AXG columns + NucleoBond Buffer Set IV for isolation of genomic DNA from tissue

More Information

  NucleoBond AXG 20 NucleoBond AXG 100 NucleoBond AXG 500
Technology Anion-exchange technology
Format Mini gravity-flow columns Midi gravity-flow columns Maxi gravity-flow columns
Starting material 2–5 ml bacterial culture
3–5 ml yeast culture
<20 mg tissue
15–20 ml bacterial culture
10–20 ml yeast culture
<100 mg tissue
60–80 ml bacterial culture
100–500 ml yeast culture
<400 mg tissue
Fragment size 500 bp–300 kb 500 bp–300 kb 500 bp–300 kb
Typical yield 20 µg 100 µg 500 µg
A260/280 1.80–1.95 1.80–1.95 1.80–1.95
Preparation time 4–5 hr 4–5 hr 4–5 hr
Binding capacity 20 µg 100 µg 500 µg

Applications

  • Isolation of genomic DNA from bacteria, yeast, and tissue

Additional product information

Please see the product's Certificate of Analysis for information about storage conditions, product components, and technical specifications. Please see the Kit Components List to determine kit components. Certificates of Analysis and Kit Components Lists are located under the Documents tab.