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The Fast Ion Plasmid Maxi Kit (Endotoxin Free) uses pre-packed anion exchange resin columns to purify plasmid DNA from 100-250 ml of bacterial cultures. Modified alkaline lysis method (1) and RNase treatment are used for obtaining clear cell lysate with minimal genomic DNA and RNA contaminants. Once the plasmid DNA has been bound to the column, the contaminants can be washed off using the wash buffer. Finally, the purified plasmid DNA is eluted by a high salt buffer and precipitated with isopropanol for desalting. The entire procedure can be completed in 120 minutes and the obtained high purity plasmid DNA is suitable for transfection, sequencing reactions, PCR and in-vitro transcription.
Specifications: |
Endo Free Midi |
Endo Free Maxi |
Sample: |
50ml culture for high-copy |
100ml culture for high-copy |
100ml culture for low-copy |
250ml culture for low-copy |
|
Yield: |
up to 200ug of plasmid DNA |
500ug to 1mg of plasmid DNA |
Format: |
gravity flow |
gravity flow |
Time: |
approx 120 min. |
approx 120 min. |
The 96-Well Genomic DNA Kits are designed for high-throughput purification of total DNA (including genomic, mitochondrial and viral DNA) from whole blood and a variety of animal tissues or cells. This method uses Proteinase K and a chaotropic salt to lyse cells and degrade proteins. DNA in the chaotropic salt is bound by the glass fiber matrix of each well. Once any contaminants have been removed, the purified DNA is eluted by a low salt elution buffer or water. The entire procedure can be completed in 1 hour without phenol extraction or alcohol precipitation. These kits can be used for manual filtration or with robotic handling systems, and purified DNA with approximately 20-30kb is suitable for PCR or other enzymatic reactions.
Sample Size: |
Up to 25mg of animal tissues, mouse tails or swabs |
Format: |
96-Well Plates |
Operation: |
Centrifuge/Vacuum manifold |
Binding Capacity: |
Up to 30ug per well |
Operation Time: |
60 minutes |
The Genomic DNA Mini Kit for Plants provide a quick and easy method for purifying total DNA (including genomic DNA, mitochondrial and chloroplast DNA) from plant tissue. Samples are disrupted by both grinding in liquid nitrogen and lysis buffer incubation. The lysate is treated with RNase A to degrade RNA and then filtered to remove cell debris and salt precipitates. In the presence of the binding buffer, coupled with chaotropic salt, genomic DNA in the lysate binds to the glass fiber matrix of the spin column. Contaminants are removed using a Wash Buffer (containing ethanol) and the purified genomic DNA is eluted by a low salt Elution Buffer or TE. The procedure does not require DNA phenol extraction or alcohol precipitation, and can be completed in less than 1 hour. The purified genomic DNA is ready for use in PCR, Real-time PCR, Southern Blotting and RFLP.
|
MINI |
MAXI |
Sample Size: |
up to 100mg fresh plant tissue/ |
up to 1g of fresh plant tissue/ |
Format: |
Spin Column |
Spin Column |
Expectant Yield: |
up to 50µ g DNA |
up to 140µ g DNA |
Operation Time: |
60 min or less |
60 min |
The Genomic DNA Mini Kit for Tissue was designed specifically for purifying total DNA (including genomic, mitochondrial and viral DNA) from a variety of animal tissue, paraffin-embedded tissue, buccal swab and amniotic fluid. The provided micropestle can efficiently homogenize tissue samples to shorten the time in the Lysis Step. Proteinase K and chaotropic salt are used to lyse cells and degrade protein, allowing DNA to be easily bound by the glass fiber matrix of the spin column. Once any contaminants have been removed, using a Wash Buffer (containing ethanol), the purified DNA is eluted by a low salt Elution Buffer or TE. The entire procedure can be completed within 1 hour without phenol/chloroform extraction or alcohol precipitation. The expected yield of genomic DNA is up to 50µg and the purified DNA (with approximately 20-30 Kb) is suitable for use in PCR or other enzymatic reactions.
Sample Size: |
Up to 50mg of tissue or 200ul of blood |
Format: |
Spin Column |
Expectant Yield: |
up to 50µ g DNA in 50-200µ l |
Operation Time: |
60 min or less |
The Genomic DNA Kit for Blood or Cultured Cells provides an efficient method for purifying total DNA (including genomic, mitochondrial and viral DNA) from whole blood, frozen blood, buffy coat, cultured animal/bacterial cells and fungus. Chaotropic salt is used to lyse cells and degrade protein, allowing DNA to bind to the glass fiber matrix of the spin column. Contaminants are removed using a Wash Buffer (containing ethanol) and the purified genomic DNA is eluted by a low salt Elution Buffer or TE. The entire procedure can be completed in 1 hour without phenol/chloroform extraction or alcohol precipitation, with an average DNA yield of 6 µ g from 200 µ l of whole human blood and up to 50µ g of DNA from 200µ l of buffy coat. Purified DNA, with approximately 20-30 Kb, is suitable for use in PCR or other enzymatic reactions.
|
MINI |
MAXI |
Sample Size: |
up to 300µ l fresh whole blood, up to 10 cultured cells |
10ml frozen blood, up to 10 cultured cells |
Format: |
Spin Column |
Spin Column |
Expectant Yield: |
up to 50µ g DNA in 50-200µ l |
up to 140µ g DNA in 1-2ml |
Operation Time: |
40 min or less |
60 min or less |
SealPlate® RollMate™ Pre-scored Film in a Convenient, Easy to Use Roll Format
Pre-scored film on a roll is a more economical and efficient alternative to rapidly seal microplates or racked test tubes; faster than applying single sheeted film. Self-standing, non-slip supports hold the pre-scored film roll securely in place for quick and easy bench-top dispensement. The roll unwind tension can be easily adjusted to user preference. Continuous backing liner can be torn off or fed directly into a waste basket for disposal.
- Economical
- Quicker, more efficient sealing
- Provides a secure seal and is easy to remove
- Rigid polyester film features good clarity and easy handling
- Can be used as a temporary seal while awaiting further processing
- General laboratory use
- Short-term storage
- Incubation
- ELISA
- -40°C to +120°C
- Higher sensitivity
- Use in the same way as EtBr in agarose gel electrophoresis
- Detection of DNA and RNA
- Safest DNA stain by far
- Low cost
- 10,000X
- Excitation wavelengths at 290nm and 490nm
DNA SafeStain Plus is a highly sensitive green fluorescent DNA/RNA staining reagent for detecting nucleic acids in agarose and polyacrylamide gels. This unique stain gives high sensitivity for detection of double-stranded or single-stranded DNA and RNA. Gels can be post-stained or the stain can be added to gels during gel casting or to the gel running buffer. DNA SafeStain Plus has two excitation wavelength peaks at about 290nm and 490nm, and an emission wavelength at 530nm, making it compatible with a standard UV light box, a blue-light transilluminator, or a gel reader equipped with visible light excitation; such as, a 488 nm laser-based gel scanner.
DNA SafeStain Plus is in a 10,000X concentrated format that can be easily diluted 10,000 times for use in precast gel staining, or 5,000 times for use in post gel staining.
Samples stained with DNA SafeStain Plus are compatible with downstream molecular biology applications; such as, gel extraction, and cloning.
- Safest DNA stain by far
- Replaces EthBr in agarose gel electrophoresis
- Detection of DNA and RNA
- Excitation at 290nm & 490 nm
- Emission at 530nm
DNA SafeStain is a new and safe nucleic acid stain for visualization of double-stranded DNA, single-stranded DNA, and RNA in agarose gels. The dyes are developed to replace toxic ethidium bromide (EthBr, a potent mutagen), commonly used in gel electrophoresis for visualization of nucleic acids in agarose gels. DNA SafeStain is non-carcinogenic by the Ames-test. The results are negative in both the mouse marrow chromophilous erthrocyte micronucleus and mouse spermary spermatocyte chromosomal aberration tests.
DNA SafeStain emits green fluorescence when bound to DNA. It has two excitation wavelength peaks when bound to nucleic acid, at 290nm and 490nm and the emission can be detected at 530nm.
Storage:
Store under dark at 4°C or room temperature.
User Instruction:
DNA SafeStain can be used in the exact same way as EtBr in agarose gel electrophoresis. For example, add 100µl to 1 liter of 1X running buffer (1xTAE or 1x TBE), and use this DNA SafeStain containing buffer to make the agarose gel and run the gel.
Special Notes:
1. For best results, dilute the DNA SafeStain 1:10,000 in your gel running buffer and use this dye-containing running buffer to make your agarose gel and to run the gel.
2. As is the case with EtBr; add more DNA SafeStain, if brighter DNA bands are desired. To view the results, any conventional DNA gel viewing light box or gel documentation system should work well with the DNA SafeStain; although, using a LED light instead of a UV light source is preferred due to the harmful nature of UV light.
This Product is For Research Use Only
For the proper disposal of this product, follow University or Company Guidelines.
EZcap™FoilStrips
An economical and more user-friendly alternative to PCR strip caps; no sore thumbs and fingers guaranteed!
- Certified DNase- & RNase- free
- Each sheet contains 6 strips on a continuous liner for ease of use
- Pierceable with a pipet tip or robotic probe for direct sample recovery
- The conformable nature of foil allows for the visual verification of the seal’s security around each well
- 2.0mil aluminum foil removes easily without tearing
- A non-locking workstation is recommended for sample prep (e.g. 96-well round-boom plate)
- Removal of the end-tabs at the perforations is recommended before cycling
- A final sealing step is highly recommended in the thermal cycler because 8-tube strips flex during handling
- Do not fold foil around sides of tubes
- The CleanSpot is designed to fulfill a very important laboratory need...control of PCR contamination.
- Just 25 - 30 minutes of UV irradiation in the CleanSpot can prevent unwanted PCR contamination.
- The combination of a special light reflector and two powerful overhead UV bulbs generate Pyrimidine Dimers (T,C) and other photo defects in contaminating target sequences, thus eliminating falsely primed products that result in countless lost time and expense.
- The CleanSpot is designed to prevent unwanted contaminant DNA in amplification mixtures, thereby saving many lost hours and expensive samples.
- The UV resistant acrylic enclosure provides a contained, dead air space in which to set up your reactions and permits safe 254nm UV irradiation of solutions and supplies. This powerful UV wavelength renders DNA contaminants biologically inactive in 30 minutes or less.
- The thick front panel is an effective beta irradiation shield as well as acting as a breath guard. An overhead fluorescent light illuminates the work area.
- Dimensions: 18"L x 24"W x 28"H
- 1 year warranty
AlumaSeal® CS™
- Specially formulated for cold storage to -80 °C
- Excellent barrier properties to retard evaporation
- Easily pierceable with pipet tips or robotic probes for sample recovery
The Rotocycler 72 facilitates the handling and insertion of caps on the tubes by offering a special solid aluminum loading rack. This rack can hold up to 18 x 0.1 mL tube strips for a total of 72 tubes. Other cavities can hold larger reaction tubes. To keep reactions cool during setup, simply place the rack in a refrigerated area. For easy reference, all wells are numbered. Color coding is made possible by inserting a Capinsert in up to two locations on the rack.
Includes: Rotocycler 72 and 500 assorted color coding inserts
Accessories for the Rotocycler 72
T319-4N |
Rotocycler 0.1 mL Tube and Cap Strips for Qiagen Rotor-Gene Q |
T319-72D2 |
Rotocycler 72 Rotor with 100 µL wells for Qiagen Rotor-Gene Q |
T319-100D1 |
Rotocycler 100 Rotor with 25 µL wells for Qiagen Rotor-Gene Q |