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Read The Zymo Research PromiseZR-96 Genomic DNA Clean & Concentrator-5 Kit
Cat # | Name | Size |
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Highlights
- Quick, high-throughput (96-well) recovery of large-sized DNA from any enzymatic reaction or impure preparation without messy precipitations
- Unique spin column for low volume elution of ultra-pure, high-yield DNA
- Eluted DNA is ideal for PCR, endonuclease digestion, sequencing, etc.
Documents
Product Description
Technical Specifications
Applicable For | Eluted DNA is ideal for ligation, sequencing, labeling, PCR, microarray, transfection, transformation, restriction digestion procedures, and any other sensitive downstream application |
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Elution Volume | ≥ 15 µl of DNA Elution Buffer |
Equipment | Centrifuge w/ microplate carriers |
Purity | A260/A280 > 1.8, A260/A230 > 1.8 |
Sample Source | Enzymatic reactions or impure preparations containing genomic DNA |
Sample storage | Eluted DNA can be used immediately or stored at ≤ -20°C |
Size Range | > 50 bp and up to 200 kb |
Yield | Up to 5 µg DNA. Recovery of DNA ranges from 70 - 95% |
Resources
Q1: What is the lower limit and minimal amount of DNA that can be recovered?
Picogram levels of DNA can be recovered. The limitation is based on sensitivity of detection method.
Q2: How to process naked DNA stored in DNA/RNA Shield?
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.
Q3: What to do if ethanol addition to the DNA Wash Buffer was omitted?
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.
Q4: What happens if more DNA was loaded on the columns than the stated maximum binding capacity?
Oversaturation of the column can result in total DNA loss due to clogging of silica matrix.
Q5: How many times can columns be reloaded?
We recommend no more than 5 times as binding efficiency might decrease.
Q6: What is the minimum input volume of DNA sample?
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.
Cat # | Name | Size | |
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D3004-4-4 | DNA Elution Buffer | 4 ml | |
D3004-4-1 | DNA Elution Buffer | 1 ml | |
D3004-4-16 | DNA Elution Buffer | 16 ml | |
D3004-4-10 | DNA Elution Buffer | 10 ml | |
D4003-2-24 | DNA Wash Buffer (Concentrate) | 24 ml | |
D4003-2-6 | DNA Wash Buffer (Concentrate) | 6 ml | |
D4003-2-48 | DNA Wash Buffer (Concentrate) | 48 ml | |
D5201-1-50 | ChIP DNA Binding Buffer | 50 ml | |
D5201-1-100 | ChIP DNA Binding Buffer | 100 ml | |
C2010 | Zymo-Spin I-96-XL Plates | 2 Plates | |
C2003 | Elution Plate | 2 Plates | |
C2002 | Collection Plate | 2 Plates | |
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