EXTRACTME DNA BACTERIA KIT

Index Size
EM02-010 10 preps
EM02-050 50 preps
EM02-250 250 preps

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Product Features

The EXTRACTME DNA BACTERIA kit is designed for the rapid and efficient purification of high quality bacterial DNA from broth and plate cultures as well as frozen cells. The isolation protocol and buffer formulations were optimized for high isolation efficiency and DNA purity.

 

SAMPLE MATERIAL

broth or plate bacterial culture, frozen cell pellet

 

EFFICIENCY

- up to 5x 108 cells → 100%

- 1x 109 ÷ 3x 109 → 75-90% (when the modified protocol for isolation from large number of cells is followed)

- 1x 109 ÷ 3x 109 → ≤ 60% (when the standard isolation protocol is followed)

 

BINDING CAPACITY

approx. 40 μg DNA

 

TIME REQUIRED

40-60 minutes (including incubation time)

 

DNA PURITY

A260/A280 ratio = 1.7 – 1.9

 

Principle

The DNA purification procedure consists of four steps and utilises spin minicolumns with membranes which efficiently and selectively bind nucleic acids. In the first isolation step, the cell walls, membranes and proteins are degraded by lysis buffer and Proteinase K. To obtain an RNA-free DNA sample, the RNA is removed by RNase A. After the addition of chaotropic salts, the lysate is applied to the purification column membrane and the DNA is bound. The two-step washing stage effectively removes impurities and enzyme inhibitors. The purified DNA is eluted using a low ionic strength buffer (Elution Buffer) or water (pH 7.0-9.0) and may be used directly in all downstream applications such as PCR, qPCR, Southern blotting, DNA sequencing, enzymatic restriction, ligation and so forth, or stored until ready to use.

 

Quality control

The quality of each production batch (LOT) of EXTRACTME DNA BACTERIA kit is tested using standard QC procedures. The purified DNA concentration, quality and stability are evaluated by gel electrophoresis and spectrophotometer. In addition, the functional quality is tested by qPCR and digestion with restriction enzymes.


Manufacturer: BLIRT S.A.