Our Products
Nuclear and Cytoplasmic Protein Extraction Kit is designed to quickly prepare highly enriched fractions of cytoplasmic and nuclear proteins from eukaryotic samples, such as cultured cells and fresh tissues:
Mycoplasma prevention spray of laboratory surfaces and apparaatus
Eradicates mycoplasma
Non-corrosive an non-carcinogenic
Convenient and stable
Ready-to-use
Mycoplasma are known as common contaminants in cell cultures, virus stocks, and other cell-derived biologicals. Contaminated cultures must be isolated and destroyed quickly, to avoid cross contamination, one of the main reasons for mycoplasma contamination in cell culture laboratories. Especially contaminated lab equipment and lab surfaces cause the spread out of mycoplasma. Only frequent cleansing of all used surfaces and equipment can fight and avoid mycoplasma contamination in laboratories. MycoClean™ Mycoplasma Prevention Spray is an effective solution for reliable disinfection of laboratory surfaces and apparatus including clean benches, incubators, work benches, cell storage boxes and liquid nitrogen containers. MycoClean™ shows an excellent effectiveness against mycoplasma. Contamination-fee and clean surfaces can be achieved in single application.
Spin column type product for quick and easy separation/purification of high yield of Plasmid DNA
Preparation time except Cell harvest takes only 10 minutes.
Possible to extract high purified and yield of plasmid DNA using relatively low amounts of buffer
Ice incubation, centrifugation are not necessary
Able to use extracted plasmid DNA in downstream application
Fast DNA-spinTM Plasmid DNA Purification Kit is used for purifying and separating high yield of plasmid DNA from E.Coli using silica membrane and optimized alkali lysis buffer system. Especially, experiment time has been minimized by simplifying procedure and ice incubation, centrifugation is not necessary. This product can be stored at RT for 1 year if buffer contents including Rnase A were not used. Also, Lysis & Neutralization indicator such as Lysis Viewer is included and able to verify pH change visually in real time. Purified plasmid DNA from this kit can be used for transfection, ligation, transformation, sequencing, etc. This product is suitable for PCR and restriction enzyme experiments as well.
RedSafe™ Nucleic Acid Staining Solution (20, 000x) is a new and safe nucleic acid staining solution. It is an alternative to the traditional ethidium bromide(EtBr) stain for detecting nucleic acid in agarose gels. It emits green fluorescence when bound to DNA or RNA.
This new stain has two fluorescence excitation maxima when bound to nucleic acid, one caentered at 309 nm and another at 419 nm. In addition, it has one visible excitation at 514 nm.
The fluorescence emission of RedSafe™ bound to DNA is centered at 537 nm. RedSafeTM Nucleic Acid Staining Solution (20, 000x) is as sensitive as EtBr. The protocol is also similar with a protocol of EtBr. The Ames test proves lower mutation with RedSafe™ Nucleic Acid Staining solution compare with EtBr. In addition, RedSafe™ Nucleic Acid Staining Solution (20, 000x) has a negative result in mouse marrow chromophilous erythrocyte micronucleus test and mouse spermary spermatocyte chromosomal aberration test.
Therefore, it is wise to choose RedSafe™ Nucleic acid Stainig Solution (20, 000x) instead of EtBr for detecting nucleic acid in agarose gels
Non Toxic
Non Mutagenic
Non Carcinogenic
No Hazardous Waste
Essential for EtBr decontamination in laboratory such as space and equipment surface, vitreous instrument surface
Efficiency : Quickly remove EtBr and SYBR series dye
Economical : Refillable spray type allows control of pollution source at low cost
Safety : Demonstration of blocking effect on mutagenicity through AMES Test
Simplicity : Easy to spray and wipe
EtBr Wiper is an indispensable product used to decontaminate Ethidium Bromide (EtBr) in the laboratory, such as the surfaces of space and equipment, and the surface of microscopic instruments. Ethidium bromide (EtBr), the most commonly used dye for DNA electrophoresis, has very strong genotoxicity and is classified as a mutagenic or carcinogenic substance in humans. To this end, many researchers are doing their utmost to take care of the separation and handling of the handling space There is a lot of difficulty to control the invisible pollution that occurs in the environment such as the glassware and the glassware. Of course, we use RedSafe ™ Nucleic Acid Staining Solution (Cat. No. 21141), a replacement for EtBr, but we do not give up EtBr according to your experimental environment and preferences.
For these researchers, EtBr WiPER is a Lab Well-being product that can completely remove EtBr by spraying and wiping it with contamination source. This product quickly and efficiently decomposes EtBr into the human body as hypoallergenic. It is also very easy to spray and wipe to control the lab's long-suffering EtBr. This product is suitable for the experimental space such as the table where EtBr is contaminated.
Essential product of RNA work which can easily remove RNase from experiment device and vitreous surface Effective removal of RNase contamination, which is likely to occur through the environment
No DEPC with high concentration of detergent, strong acid or carcinogen
Ready to use
Available in a spray ready for immediate use Spray / Rinse or Wipe
Remove the contamination source just by spraying on the surface to be cleaned and then rinsing or wiping
Easily applicable to plastic, glass, pipette, etc. which are difficult to sterilize
RNase as well as unwanted DNA contamination can be effectively removed
RNase WiPER ™ is used to remove RNase, a major source of contamination that has a major impact on the results of experiments with RNA work, from the surface of the laboratory, instrument, and various horses. It is a simple product that is sprayed locally and sprayed where pollution is expected or where contamination is needed, but it is very effective for removing RNase contamination. RNase WiPER ™ does not use DEPC with high concentration of detergent or carcinogen, so it is easy to spray and relatively safe for the experimenter. In addition, since it does not use strong acid, it is not only highly safe but also has no effect on subsequent experiments. This product is intended to maintain the compatibility of surrounding environment during various RNA work, but it is a chemical different from RNase inhibitor and it is prohibited to inject directly into the reaction solution of the experiment.