Bacterial Genomic DNA Kit

The Bacteria Genomic DNA Extraction Kit provides a simple and rapid method for high quality genomic DNA isolation from Gram Positive and Gram Negative Bacteria. The Bacteria Genomic DNA system uses the silica-gel-membrane spin column technology for simple and fast isolation of Genomic DNA without phenol/chloroform. Homogenization is not necessary since tissues are directly lysed by Proteinase K.

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CAD$100.00

  • 50 preps
  • 100 preps
  • 200 preps

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The Bacteria Genomic DNA Extraction Kit provides a simple and rapid method for high quality genomic DNA purification from Gram Positive and Gram Negative Bacteria. The Bacteria Genomic DNA system uses the silica-gel-membrane technology for simple and fast isolation of Genomic DNA without phenol/chloroform. Homogenization is not necessary since tissues are directly lysed by Proteinase K. The buffer system is optimized to allow selective binding of DNA to the silica-gel membrane. The simple centrifugation protocol completely removes contaminants such as proteins, divalent cations, and secondary metabolites. Pure DNA is then eluted in water or low-salt buffer, ready to use. The typical yield of genomic DNA is 3-20 µg from 0.52 ml of bacteria culture. The purified high molecular weight genomic DNA is suitable for direct use in all common molecular biology applications: PCR, restriction digestion, cloning, DNA sequencing and Southern blot analysis.


Features


Efficient: 3-20 µg of genomic DNA from 1.52 ml bacteria culture.
Fast: Procedure takes only 30 min.
Safe: No phenol extraction step.
High purity: Purified DNA is ready for downstream application such as PCR, restriction digestion.

Downstream Applications


Purified DNA is free from contaminants and enzyme inhibitors, and typically has A260/A280 ratios between 1.7 and 1.9, and is suitable for applications such as:

ü Restriction digestion

ü PCR

ü Labeling

ü Library construction

Kit Content: (for a 50-prep kit size)

Component

Volume or Size

Solution DS

15 ml

Solution MS

20 ml

Proteinase K

1 ml

Wash Buffer (PS)

30 ml

Wash Buffer (PE)

15 ml

Elution Buffer TE

5 ml

Spin Columns

50 each


Storage


Store Protein K at -20, other reagents can be stored at room temperature for up to 1 year. Any precipitate in the Solution DS and Solution MS can be re-dissolved by incubating at 37°C before use.


Important Notes


Prior to the initial use of the kit, dilute the Wash Buffer(PE) with ethanol (96-100%):

N1151(50preps)

N1152(100preps)

Wash Buffer(PE)

15 ml

30 ml

Ethanol

45 ml

90 ml

Total Volume

60 ml

120 ml

After the ethanol has been added, mark the check box on the bottle to indicate the completed step.
Examine the solution for precipitates before each use. Re-dissolve any precipitate by warming the solution to 37°C and cooling to 25°C.
All purification steps should be carried out at room temperature.

Protocol

1. Add 0.52 ml of an overnight culture to a 1.5 ml microcentrifuge tube. Centrifuge at 12,000 rpm for 2 min to pellet the cells. Remove the supernatant.

2. Add 200 μl Solution DS to the pellet. It is essential that the sample and Solution DS are mixed immediately and thoroughly by vortexing or pipetting to yield a homogeneous solution.
Note: For Gram Positive Bacteria, resuspend the cells thoroughly in 180μl of buffer (20 mM Tris, pH 8.0, 0.2 mM EDTA, 1.2% Triton X-100) with 50 mg/ml lysozyme by vortexing. Incubate at 37 for 30 minutes.
(Optional): If RNA-free genomic DNA is required, add 4 μl RNase A (100 mg/ml) and incubate for 5 minutes at room temperature. RNase A (100 mg/ml) can be purchased separately.

3. Add 20 μl Proteinase K and 220 μl Solution MS. Mix thoroughly by vortexing. Incubate at 65°C for 10 minutes to yield a homogeneous solution. Spin down the water beads on the wall of the tube.

4. Add 220 μl ethanol (96100%) to the sample, and mix thoroughly by vortexing. It is important that the sample and the ethanol are mixed thoroughly. A precipitate may appear. Pipet the mixture from step 4 into the spin column placed in a 2 ml collection tube (provided). Centrifuge at 12,000rpm for 1 min. Discard flow-through.

5. Add 500 μl Wash Buffer PS, and centrifuge for 1 min at 12,000 rpm. Discard flow-through.

6.Add 500 μl Wash Buffer PE, and centrifuge for 1 min at 12,000 rpm. Discard flow-through. Repeat step 6 again.

7. Centrifuge for 3 min at 12,000 rpm to dry the column membrane. Discard flow-through and collection tube.
Note It is important to dry the membrane of the spin column, since residual ethanol may interfere with subsequent reactions. This centrifugation step ensures that no residual ethanol will be carried over during the following elution. Following the centrifugation step, remove the spin column carefully so that the column does not come into contact with the flow-through, since this will result in carryover of ethanol. If carryover of ethanol occurs, empty the collection tube, then reuse it in another centrifugation for 1 min at 12,000 rpm.

8. Place the spin column in a clean 1.5 ml microcentrifuge tube (not provided), and pipet 30-100 μl Eluent Buffer AE (prewarm to 65) directly onto the membrane. Incubate at room temperature for 2 minutes, and then centrifuge for 2 min at 12,000 rpm to elute. The tube contains the purified DNA. Store the DNA at -20℃.

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