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View additional product information for RiboPure™ RNA Purification Kit - FAQs (AM1924)
7 product FAQs found
RNA质量/纯度差通常是由于以下原因:
•RNA部分降解:应使用新鲜的组织或细胞,或在无法立即冻存组织的情况下使用RNAlater溶液保存样品。
•DNA污染:如果样品含有机溶剂、强力缓冲液或碱性溶液,我们推荐在8°C下进行液相分离。
•A260/A280比值低(<1.6):这表示TRI Reagent用量不足。在室温下孵育匀浆液5分钟,有助于核蛋白从RNA上解离。苯酚污染也会引起吸光度比值降低。
柱分离临界尺寸为200 nt。RiboPure试剂盒不适用于回收miRNA。我们推荐使用mirVana试剂盒、TRIzol Plus RNA纯化试剂盒或PureLink RNA微量提取试剂盒分离miRNA。
PureLink RNA小量提取试剂盒提供快速的总RNA柱纯化,无需有机溶解(苯酚/氯仿)。单次提取可获得多达1,000 µg的纯化RNA。RiboPure RNA纯化试剂盒结合了苯酚/硫氰酸胍溶液和玻璃纤维过滤纯化法。
Poor quality/poor purity RNA is typically due to the following:
- Partially degraded RNA: Use fresh tissue or cells, or use RNAlater Stabilization Solution if tissue cannot be frozen immediately.
- DNA contamination: If the sample contains organic solvents, strong buffers, or an alkaline solution, we recommend performing phase separation at 8 degrees C.
- A low A260/A280 ratio (<1.6): This indicates that an insufficient amount of the TRI Reagent was used. Incubation of the homogenate at room temperature for 5 minutes can help nucleoproteins dissociate from RNA. Phenol contamination could also cause a low absorbance ratio.
The column cut-off size is 200 nt. Using a RiboPure kit is not appropriate for miRNA recovery. For miRNA isolation, we would suggest using a mirVana kit, the TRIzol Plus RNA Purification Kit, or the PureLink RNA Micro Kit.
The PureLink RNA Mini Kit provides rapid column-based purification of total RNA, without organic lysis (phenol/chloroform). You can obtain up to 1,000 µg of purified RNA from a single extraction. The RiboPure RNA Purification Kits combine a phenol/guanidine thiocyanate solution with a glass-fiber filter purification method.
The elution buffer composition is proprietary.