AG-DNA Binding Column I

Details:

1.Technology: Silica-membrane technology

2.Format: Mini Spin Column

2. Fragment Size: 50bp-50kbp

3. Banding capability: 30ug-40ug

Applications
• Purification of Genomic, Bacterial, Viral DNA

• Purification of DNA from Whole blood, Serum, Plasma

• Purification

• DNA suitable for PCR, Southern blotting, enzymatic reactions, cloning, ect.

Specification

1. DNA mini binding Columns for DNA extraction

2. Silica-based DNA Binding Column

3. High yield and purity guaranteed

4. Very High Performance and Stability for Long-term Storage.

5. High-loading capacity

no more spill-over and cross contamination

no extra steps for processing

6. High qualify for DNA purification and has been used extensively in house application and by many academic labs.

7. Compatible with other company buffer (Qiagen, Sigma, Promega ect).

8. Economical for large sample process.

Features

1. Plastic centrifuge tube made from high quality PP material

2. Flat top design together with a large white writing area for sample identification

3. High recoveries for fragments down to 50bp

4. Max rotate speed up to 12,000g

5. High concentrated DNA, minimal elution volume of 15ul.

Column Supply

We use whatman GF/F: 0.7um membrane. GF/F This ultra-fine filter has a 98% retention efficiency for particles down to 0.7um in liquids.
Below is the information of GF/F:0.7ul membrane.

Grade GF/F: 0.7 µm
This high-efficiency filter will retain fine particles down to 0.7 µm. Unlike membrane filters with a comparable retention value, it has a very rapid flow rate and an extremely high loading capacity.

Because of the tight specification of 0.6 µm - 0.8 µm particle retention and pure borosilicate glass structure, GF/F is the material upon which the EPA Method TCLP 1311 for Toxicity Characteristic Leaching Procedure was developed. It remains today the filter of choice.

Recommended for DNA binding and purification. Very effective in filtering finely precipitated proteins, GF/F can be used in conjunction with GF/D as a prefilter for the successful clarification of extremely ‘difficult’ biochemical solutions and fluids, and nucleic acids.