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Highlights
- Quick (20 minute), large-scale recovery of ultra-pure DNA from PCR, endonuclease digestions, cell-free lysates, etc.
- ZR-96 Silicon-A Plate design allows DNA to be eluted at high concentrations into minimal volumes of solvent.
- Eluted DNA is well suited for use in PCR, DNA sequencing, DNA ligation, endonuclease digestion, RNA transcription, radiolabeling, etc.

Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
Highlights
- Quick (20 minute), large-scale recovery of ultra-pure DNA from PCR, endonuclease digestions, cell-free lysates, etc.
- ZR-96 Silicon-A Plate design allows DNA to be eluted at high concentrations into minimal volumes of solvent.
- Eluted DNA is well suited for use in PCR, DNA sequencing, DNA ligation, endonuclease digestion, RNA transcription, radiolabeling, etc.

Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
Cat # | Name | Size | Price | Quantity |
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Cat # | Name | Size | Price | |
---|---|---|---|---|
D4003-2-24 | DNA Wash Buffer (Concentrate) | 24 ml | $38.50 | |
D4004-1-L | DNA Binding Buffer | 100 ml | $66.50 | |
D4003-2-48 | DNA Wash Buffer (Concentrate) | 48 ml | $70.00 | |
C2001 | Silicon-A Plate | 2 Plates | $150.60 | |
C2003 | Elution Plate | 2 Plates | $22.10 | |
C2002 | Collection Plate | 2 Plates | $25.60 | |
Description
Performance
Technical Specifications
Detergent Tolerance | ≤5% Triton X-100, ≤5% Tween-20, ≤5% Sarkosyl, ≤0.1% SDS |
---|---|
Elution Volume | ≥ 30 µl for shallow well, ≥ 10 µl for deep well |
Equipment | Centrifuge with microplate carriers |
Purity | A260/A280 > 1.8 |
Sample Source | DNA from PCR, endonuclease digestions, DNA modification reactions, isotope/fluorescence labeling reactions, etc. |
Size Range | 75 bp to 23 kb for shallow well, 50 bp to 23 kb for deep well |
Yield | ≤ 5 µg total DNA can be recovered. For DNA 75 bp to 10 kb the recovery is 70-90%. For DNA 11 kb to 23 kb the recovery is 50-70%. |
Resources
Documents
FAQ
Picogram levels of DNA can be recovered. The limitation is based on sensitivity of detection method.
Add an equal volume of ethanol (95-100%) to the sample and mix well. The sample is ready-to-bind and does not require DNA Binding Buffer. Proceed to Step 2.
The DNA will be eluted off the column. Rebind samples using the appropriate amount of DNA Binding Buffer and wash the column with the properly prepared wash buffer.
Oversaturation of the column can result in total DNA loss due to clogging of silica matrix.
We recommend no more than 5 times as binding efficiency might decrease.
Working with volumes below 50 µl can result in decreased recovery. We recommend raising the starting volume to 100 µl with water to ensure optimal binding conditions.
Citations
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