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
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.
|RNase WiPER™||200 ml x 2 ea|
Effective way to prevent Rnase contamination
After applying RNase-WiPER ™ to the experimental horseradish to observe the effect on the subsequent stage, it was confirmed that it is possible to remove the contamination effectively by spraying and wiping it on the contaminated horseradish.
|1||O / N Soaking with RNase WiPER Used without rinsing|
|2||When RNase WiPER was used after rinsing with O / N Soaking after DW|
|3||Using RNase WiPER and Kimwipe|
|4||Washing with DW after using RNase WiPER and Kimwipe|
|6||Use contaminated product|
Effective way to remove DNA contamination
As a result of RNase-WiPER ™ treatment of the DNA solution and the presence of DNA in the residue, it is possible to find effective DNA only by treating RNase-WiPER ™.
|1||Residue after using RNase WiPER|
|2||Residue after washing with distilled water|
|3||Remained DNA after 10 μl RNase WiPER|
|4||Remained DNA after 10 μl RNase WiPER + 1ug DNA|
|5||10 μl DW + 1μg DNA (control)|