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Highlights
- Simple, high-throughput (96-well) method for efficient isolation of DNA from insects, including mosquitoes, bees, lice, ticks, and D. melanogaster .
- Compatible with tough-to-lyse tissues from other organisms.
Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
Highlights
- Simple, high-throughput (96-well) method for efficient isolation of DNA from insects, including mosquitoes, bees, lice, ticks, and D. melanogaster .
- Compatible with tough-to-lyse tissues from other organisms.
Original Manufacturer
Innovated in California, Made in the USA
Satisfaction 100% guaranteed, read Our Promise
| Cat # | Name | Size | Price | Quantity |
|---|
| Cat # | Name | Size | Price | |
|---|---|---|---|---|
| S6002-96-2 | ZR-96 BashingBead Lysis Rack | 2 mm | $224.00 | |
| C2003 | Elution Plate | 2 Plates | $22.10 | |
| C2002 | Collection Plate | 2 Plates | $25.60 | |
| C2001 | Silicon-A Plate | 2 Plates | $150.60 | |
| P1001-2 | 96-Well Block | 2 Blocks | $21.00 | |
| C2007-4 | 96-Well Plate Cover Foil | 4 Foils | $10.30 | |
| D6001-3-40 | BashingBead Buffer | 40 ml | $33.90 | |
| D3004-5-50 | DNA Pre-Wash Buffer | 50 ml | $30.40 | |
| D3004-4-10 | DNA Elution Buffer | 10 ml | $16.40 | |
| D3004-2-100 | g-DNA Wash Buffer | 100 ml | $35.00 | |
| D3004-1-150 | Genomic Lysis Buffer | 150 ml | $85.20 | |
Description
Performance
Technical Specifications
| Applicable For | All sensitive downstream applications such as qPCR and Next-Generation sequencing. |
|---|---|
| Elution Volume | ≥ 25 µl |
| Equipment | Centrifuge with microplate carriers, 96-well plate/block disruptor or pulverizer. |
| Purity | A260/A280 nm ≥1.8. |
| Sample Source | Insect or solid tissue |
| Sample Storage | DNA stored at ≤ -20°C. |
| Size Range | Capable of recovering genomic DNA up to and above 40 kb. Typical fragment sizes range from 25 kb - 35 kb. If present, parasitic and viral DNA will also be recovered. |
| Type | Total DNA |
| Yield | 5 µg total DNA |
Resources
Documents
FAQ
A viscous sample can indicate incomplete sample lysis. Try using less of your sample and optimize bead beating conditions (duration, speed, time) to ensure samples are thoroughly lysed. After bead beating, pellet the cell debris before moving on. Adding more Genomic Lysis buffer to the lysate can help dilute and deproteinate the sample, making the sample less viscous and more suitable for DNA recovery.
Addition of beta-mercaptoethanol is recommended to enhance sample lysis, but can be substituted with dithiothreitol (DTT, final concentration of 10 mM). However, if bead beating is optimized and lysis is efficient, the addition of BME is not necessary and can be omitted.
No additional RNase A treatment is required when processing samples within kit capacity. The selective chemistry allows for binding of double stranded DNA to the column and for RNA to flow through.
Citations
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