RNase Residue Quantitative Assay Kit
Cat.No:R8600 Solarbio
Storage:-20℃
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Nucleic Acid Extraction/Purification >
Extraction/Purification Auxiliary reagent >
RNase Residue Quantitative Assay KitStorage:-20℃
Qty:
Size:
Storage | -20℃ |
Note | 1. It is recommended to test ribonuclease activity in a relatively clean environment such as a super-clean workbench or biosafety cabinet, so as to avoid the influence of ribonuclease on the samples to be tested. 2. 10×ReactionBuffer, RNaseSubstrate, and RNase-free ddH2O are either fully balanced to room temperature before use. It is recommended that RNaseSubstrate be centrifuge for a few seconds before use for the first time. 3. Please pay attention to prevent the reagent from being contaminated by RNase during operation. If necessary, nuclease scavengers can be used to remove RNase existing in the environment before each experiment. 4. 96-hole blackboard is recommended for testing. 5. Pay attention to personal protection during the experiment. |
Unit | Set |
Specification | 100T |
Ribonuclease (RNase) is a class of nucleases that catalyzes the degradation of RNA into small fragments. The RNase family includes RNaseA, RNaseB, RNaseC, RNaseH, S-RNase, RNaseP, RNaseT, etc. Among them, RnaseA is a widely used endonuclidenase. RNaseA efficiently and specifically catalyzes the break of phosphodiester bonds on the single-stranded RNA skeleton at the 3' end of pyrimidine nucleotide residues C and U to form oligonucleotides with 2', 3' -cyclic phosphate derivatives. At present, the common RNase residue detection methods mainly include radioisotope method, spectrophotometry, fluorescence quenching method and electrochemical method. The RNase residue quantitative detection kit provided by Solarbio is a rapid and highly sensitive detection kit for RNaseA activity by fluorescence method with high sensitivity and the lowest detection limit as low as 0.078pg RNase. The substrate is a synthetic RNA oligonucleotide probe with a FAM Fluorophore (Donor) at one end and a TAMRA Quencher (Acceptor) at the other end. The absorption spectra of the two groups overlap to a certain extent, and when the distance between the two fluorophores is appropriate, the fluorescence energy is transferred from the donor to the acceptor, resulting in the fluorescence intensity of the donor fluorescence molecule itself decays. When the substrate was cut by RNase, the end and end of the substrate were separated, the two groups were separated, the fluorescence of FAM was no longer damped by TAMRA, and the fluorescence of FAM could be detected. The increase rate of the fluorescence signal was positively correlated with the amount and activity of the enzyme.
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
2. For your safety and health, please wear laboratory clothes, disposable gloves and masks.
3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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