Cytiva provides three silica-based kits for DNA cleanup. illustra™ GFX™ PCR and Gel Band Purification Kit purifies PCR products and other DNAs from solution or gel slices. This product is discussed in more detail below. illustra™ GFX 96 PCR Purification Kit purifies PCR products from solution in a 96-well format, allowing for increased throughput. illustra™ CyScribe™ GFX Purification Kit is designed for cleanup of Cy3- or Cy5- dye-labeled cDNA prior to microarray or other applications.
illustra™ GFX PCR DNA and Gel Band Purification Kit is designed for the purification and concentration of DNA from PCR mixtures, restriction enzyme digests, solutions, and agarose gel bands. DNA ranging in size from 50 bp up to 10 kbp can be purified from solution volumes of up to 100 μL and from gel slices of up to 900 mg. No modifications are required for purification of DNA from gels run in borate-based buffers (e.g., TBE).
The developed method uses a chaotropic agent to extract DNA from solution and/or to dissolve agarose and to denature proteins. DNA binds selectively to the silica membrane contained in an illustra™ GFX MicroSpin column. The matrix-bound DNA is washed with an ethanolic buffer to remove salts and other contaminants, and the purified DNA is eluted in a low-ionic-strength buffer.
When purifing a PCR fragment less than 50 bp (but greater than 10 bp), use an illustra™ MicroSpin G-25 Column.
This kit cannot be used for the purification of RNA.
If handling large numbers of samples in solution, 100 bp–10 kbp in length, use illustra™ GFX 96 PCR Purification Kit.
Before first use, add absolute ethanol to the bottle containing wash buffer type 1. See product instructions for volume. Mix by inversion. Indicate on the label that this step has been completed. Store upright and airtight.
Note: Buffers and columns are NOT transferable between Cytiva kits in the illustra™ product range. Please ensure you use the correct buffers and columns for your purification.
a. From solution: Add Capture Buffer to prepare the sample for binding. Capture Buffer contains chaotropic salts that denature proteins (including enzymes) and promote adsorption of DNA to the silica matrix.
If the sample contains DNA greater than 5 kb, do not vortex, as this will cause shearing of the DNA.
b. From agarose: Add Capture Buffer to dissolve agarose and prepare the sample for binding. Incubate/mix at 60 °C until agarose dissolves.
Add sample from step 1 to the GFX column. Centrifuge. DNA greater than 50 bp binds to the silica membrane in the presence of chaotropic salts.
Wash the matrix-bound DNA with an ethanolic buffer to remove salts and other contaminants.
Note: the membrane should be free of liquid following the centrifugation step to ensure that ethanol is not eluted into the purified DNA.
Wash and dry steps can be repeated when purity is paramount, for example if the sample is to be used in a blunt-ended ligation.
Elute DNA from the membrane using 10 to 50 μL of a low-ionic-strength elution buffer. Incubate briefly at room temperature and centrifuge to elute purified DNA. In the absence of chaotropic salts, DNA desorbs from the membrane.
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