Details:

Technology: Silica-membrane technology

Format: Mini Spin Column

Fragment Size: 50bp-50kbp

Banding capability: 40ug-50ug

 

Applications
Purification of DNA from Plasmid, Bacteria

Purification of DNA from Whole blood, Serum, Plasma

Purification of DNA from Agarose Gel, PCR Products

Purification of DNA from Tissue, cells, stool, urine, forensic, FFPE samples

DNA suitable for PCR, Southern blotting, enzymatic reactions, 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. Max rotate Speed up to 12,000g

 

 

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 m
this high-efficiency filter will retain fine particles down to 0.7 m. 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 m - 0.8 m 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.